US2703270A - Production by spinning of cellulose hydrate filaments - Google Patents

Production by spinning of cellulose hydrate filaments Download PDF

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Publication number
US2703270A
US2703270A US301364A US30136452A US2703270A US 2703270 A US2703270 A US 2703270A US 301364 A US301364 A US 301364A US 30136452 A US30136452 A US 30136452A US 2703270 A US2703270 A US 2703270A
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United States
Prior art keywords
filaments
stretching
viscose
spinning
cellulose
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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
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US301364A
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English (en)
Inventor
Studer Martin
Willimann Louis
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.)
Viscosuisse SA
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Societe de la Viscose Suisse SA
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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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S264/00Plastic and nonmetallic article shaping or treating: processes
    • Y10S264/27Process of spinning viscose where viscose has high degree of polymerization

Definitions

  • the present invention relates to a spinning process for the production of filaments of all kinds from viscous solutions which are characterised by a highly oriented crystalline structure and in consequence a high tensile strength, and to the filaments so obtained.
  • the term filaments as used herein is to be understood to. cover multiple and single filaments, fibres, small ribbons and foils.
  • viscose filaments having a relatively high stretching capacity and tensile strength up to about 3.5 g./den. in the dry condition and about 2.0 g./den. in the wet condition. This is frequently achieved by softening and simultaneously stretching the freshlyspun thread in one or more baths at temperatures which may be, for example, higher than 70 C.
  • Other processes employ spinning baths which either have a high content of, zinc sulphate or have, a minimal coagulating action on the viscose solution. The object of all these processes is to make it possible to subject the thread to a high degree of stretching during the spinning, operation itself or immediately after that operation. However, there is 111 practice a limit. to the amount of stretch that can.
  • a processv for the production of filaments of high stretching capacity and high tensile strength comprises spinning through spinnerets a viscose of gamma number above 60 in such a manner that the degree ofpolymerisation of the filament is above 300 into a spinning bath of low electrolyte content and stretchingthe filaments continuously with their formation, the spinning being effected at room temperature and the stretching of the filaments being effected so that the speed of travel of the filaments afiter such stretching is not greater than 12 metres/ minute.
  • the gamma number is the number of mols of CS2 combined per glucose radical multiplied by 100.
  • Viscose solutions of gamma number above 60 may have a cellulose content of about 4 to 11% by weight and a caustic soda con-tent of about 3 to 12% by weight, that is to say, they are of normal composition. Wood pulp or linters or othervcellulose products employed in the viscose industry are used as cellulose-containing starting materials. The production of the viscose solutions is eifected in the usual manner.
  • Cellulose xanthate containing cellulose of high molecular weight is particularly useful and is obtained by treating a material containing cellulose of high molecular weight with caustic soda and omitting the ripening of the alkali cellulose.
  • the average degrees of polymerisation of the cellulose hydrate regenerated from the alkali cellulose or the viscose are, in accordance with this invention, above 300. 7
  • These viscose solutions are spun into baths which have a weak coagulating action, a low sulphuric acid content and a relatively low electrolyte content and which are operated at room temperature, by which is meant about 10 to 25 C.
  • the sodium sulphate concentration is preferably kept below 100 g./lt.
  • Such metal salts as Zinc sulphate, iron sulphate, aluminium. sulphate and magnesium sulphate which tend to reduce the stretchability of the filament are avoided.
  • the sulphuric acid concentr ation is preferably 1 0 to 40 g./lt. Substances such as lau'ryl pyridium chloride or sulphate, which facilitate spinning may be added to the spinning bath.
  • the filaments obtained may be stretched, in, accordance with the invention by more than 1.50% and preferably. 200% to 400% if individual filaments of less. than 10 denier are required. For the production. of single filaments, or small ribbons or the like above 10 denier, the stretch must be reduced.
  • the speed of the filaments after the, stretching operation is, less than 12 metres per minute and preferably 4 to 7 metres per minute.
  • the speed of the filaments after the, stretching operation is, less than 12 metres per minute and preferably 4 to 7 metres per minute.
  • For a stretch of 200-400% at 4 to 7 metres per minute final speed it is necessary on the one hand to make the distance between the spinneret and the point where the stretch is initiated as. small as possible and, on the other hand, to establish arninimum period of 3 seconds during which the thread is. subjected to tension.
  • the necessity for these stretching conditions may perhaps be explained on the.
  • the high degree of stretch is only possible and elfective when the filament to bestretched has a relatively high concentration of Xant-hate groups and that the stretching tension must be elfective while a relatively large part of these Xanthate. groups is. being split off.
  • the distance between, the spinneret andthe place where the stretching is initiated may be adjusted, within the abovedescribed limits according to the gamma number of the viscose solution at the composition. and temperature of the spinning bath. In this connection, the lower the concentration of the ester groups at the point where the stretching commences, the
  • the filament can be stretched by friction by means of tubular rods or between driven rolls or pairs of rolls rotating at different peripheral speeds or by a combination of both systems. During the stretching the filament can move forward partially or wholly in the spinning bath or partially or wholly in the air.
  • the filament can be drawn off vertically or horizontally through the spinning bath from the spinneret, or at any intermediate angle.
  • the spinnerets are of the usual construction. Where multiple hole spinnerets are employed, they are so located that the gases formed during the spinning may readily escape.
  • the stretched filaments are spooled in any suitable manner.
  • a sulphite pulp with 89% a-cellulose content was employed.
  • the viscose solution was adjusted to 6.1% cellulose and 7.7 caustic soda content. Its gamma number at the moment of spinning was 75.
  • the cellulose regenerated from the viscose solution had a degree of polymerisation of 650.
  • the spinning bath contained 20 g. sulphuric acid and g. sodium sulphate per litre. Its temperature was C. and the thread of 300/200 den.
  • the holes of the spinneret had a diameter of 0.07 mm., the bath path was 10 cm. and the distance between the spinneret and the place where the stretching commenced was 40 cm.
  • Stretching was carried out in air between two driven stretching rolls, the spacing of which was 120 cm.
  • the threads were spooled with very slight tension on rollers and then washed free from acid, de-sulphurised, soaped and dried. The following measurements were made on the dried test pieces.
  • test piece B An X-ray diagram with CuK a-radiation was made on test piece B.
  • a diagram was obtained with a large number of clearly perceptible reflections of the first, second, third and fourth layer lines.
  • the intensity and length of the interferences show up a very high proportion of crystallised cellulose and a very high degree of orientation of the crystallites such as has not been known hitherto with viscose filaments.
  • Example I A sulphite pulp with 89% content of a-cellulose is mercerised at 18 C. and then shredded at 0 C. The alkali cellulose is then immediately xanthogenated for 2 /2 hours with 60 parts CS2 to 100 parts a-cellulose and dissolved by stirring in four hours at a temperature of 5 C. After dissolving, the gamma number is 75. The viscose solution containing 6.1% a-cellulose and 7.7% NaOI-I is filtered, deaerated and spun with a gamma number of 70 and at a viscosity of 220 poises (measured at 20 C.).
  • a filament bundle of 10,500 den. with 7,000 individual filaments is spun from a spinneret, the holes of which have a diameter of 0.07 mm.
  • the spinning bath contains 18 g. H2804, 90 g. NazSOr and 2.5 mg. lauryl pyridinium sulphate per litre. Its temperature is 20 C. and the bath path 10 cm. The distance between the spinneret and the point at which stretching commences is 30 cm. Stretching is carried out between driven rolls which are arranged at a distance of 120 cm. from one another. The degree of stretch is 300% and the spinning speed after stretching 5 m./min. The tension on the bundle with a stretch of 300% amounts to 0.78 g./den.
  • the bundle is drawn off vertically from the spinning nozzle and then vertically towards the stretching members.
  • the bundle produced in this manner is relieved of tension after the stretching and is continuously cut to 40 mm. staple lengths in the acid condition.
  • the fibres are washed free from acid and salt in the usual manner, de-sulphurised, treated with an aqueous solution containing for example 5 g./litre cetyl alcohol sulphate and dried.
  • the fibres have the following properties:
  • Example II The preparation of the viscose solution is carried out in the same manner as in Example 1.
  • the viscose solution is spun from a spinneret with 200 holes having a diameter of 0.07 mm. to form a thread of 300 den. into a spinning bath which contains 20 g. H2804 and 15 g. NazSO4 per litre and has a temperature of 18 C.
  • the bath path is 3 cm.
  • the distance between the spinneret and the point at which stretching commences is 23 cm.
  • the thread is drawn vertically from the spinneret and stretched horizontally between two driven rolls which have a spacing of cm.
  • the stretching amounts to 280% and the spinning speed after the stretching 4.7 m./min.
  • the thread tension during the stretching is 0.9 g./den.
  • the thread is wound with light tension on to a roller and finished in the usual manner. After the drying, it is twisted on a ring spinning machine at turns per The percentage amount of the elastic elongation in the dry condition to the total elongation was determined on a Scott tester, maintaining a recuperation period of one minute after each loading:
  • the dye-absorbing capacity of this thread has been compared with bleached cotton and with a commercial viscose thread of 120/80 den. with 97% swelling prepared by spinning into a Muller-type bath.
  • Dye solution 4.32 g./lit. solar blue GLN. Bath ratio 1:800.
  • the dye absorption in mg. per kg. thread or fibre respectively is 530:21 for the thread with 65% swelling spun in accordance with Example II, 300$ 12 for bleached cotton, 530:21 for viscose thread of 120/80 den. with 97% swelling.
  • Example III The same viscose solution is used as in Example 1, except that 0.8% titanium dioxide per kg. a-cellulose are added to it.
  • a bundle of 19,500 den. comprised of 1300 individual filaments of den. is spun from the spinneret, the holes of which have a diameter of 0.12 mm.
  • the spinneret is disposed in a bath which contains 60 g. H2804 and g. Na2SO4 per litre and which has an internal temperature of 22 C.
  • the length of the bath is 30 cm.
  • the bundle is drawn OE With an upward inclination of about 30. Directly above the bath, it is stretched by passing over and under 4 successive rods in such a manner that the braking action takes place. It is then conducted into a stretching device according to Example I.
  • the stretching between driven rolls, which follows the stretching due to the braking action, is 150%.
  • the final speed of the thread is 5 m./niin.
  • the bundle is then cut into staple lengths of 100 mm.
  • the fibres are finished in a manner similar to that set out in Example I.
  • Example IV Linters pulp is mercerised in the usual manner in 18% NaOI-I and squeezed out in order to produce an alkali cellulose containing about 31% a-cellulose and 15.5% NaOH.
  • This alkali cellulose is shredded for 110 minutes at 0 C. and immediately xanthated with 65 parts CS2 per 100 parts a-cellulose.
  • the xanthate is then dissolved in a beater device at 7 C. to form a viscose solution with 7.2% cellulose and 5.7% NaOH.
  • the filtered and deaerated viscose arrives at the spinneret with a gamma number of 70. It then has a viscosity of 370 poises (measured at 20 C.).
  • the spinning bath contains 20 g. H2804 and 1 g. NazSOs per litre. It has a temperature of 20 C.
  • the thread is drawn off vertically through the bath.
  • the first driven stretching member is disposed in the spinning bath.
  • the total length of the path of the thread in the bath is 45 cm., the distance between spinneret and the point where the 6 stretching commences is 5 cm. and the distance between the two driven stretching members is 120 cm.
  • the speed of the stretched thread is 3 m./min., the degree of stretching is 310%.
  • the finished thread, twisted with turns per metre, has the following properties: a
  • the thread can be used for tyre cords. We claim:
  • a process for the production of filaments of high organisation and high tensile strength having a degree of polymerisation above 300 which comprises extruding through spinnerets a viscose of gamma number above 60, the cellulose generated from said viscose having a degree of polymerisation above 300, into an aqueous spinning bath at room temperature containing only from 10-40 g./ litre of sulphuric acid and at most 100 g./ litre of sodium sulphate, and stretching the filaments about 240% continuously with their formation giving a final speed of 12 meters at most per minute, the filaments being maintained continuously under tension.
  • a process for the production of filaments of high organisation and high tensile strength having a degree of polymerisation above 300 which comprises extruding through spinnerets a viscose of gamma number above 60, the cellulose generated from said viscose having a degree of polymerisation above 300, into an aqueous spinning bath at room temperature containing only from 10-40 g./ litre of sulphuric acid and at most 100 g./ litre of sodium sulphate, and stretching the filaments continuously with their formation giving a final speed of 4 to 7 meters per minute, the filaments being maintained continuously under tension.
  • a process for the production of filaments of high organisation and high tensile strength having a degree of polymerisation above 300 which comprises extruding viscose at room temperature through spinnerets into an aqueous coagulating bath, the viscose having a gamma number above 60, generating cellulose having a degree of polymerisation above 300 and having a cellulose content of 4 to 11% by weight and a caustic soda content of 3 to 12% by weight, the aqueous coagulating bath containing only from 10-40 g./litre of sulphuric acid and at most 100 g./litre of sodium sulphate, stretching the filaments about 240% continuously with their formation giving a final speed of 12 meters at most per minute, the filaments being maintained continuously under tension.
  • a process for the production of filaments of high ganisation and high tensile strength having a degree of polymerisation above 300 which comprises extruding through spinnerets a viscose of gamma number above 60, the cellulose generated from the said viscose having a degree of polymerisation above 300, into an aqueous coagulating bath at room temperature containing only from 10 -40 g./litre of sulphuric acid and at most 100 g./litre of sodium sulphate, and stretching the filaments in the coagulating bath about 240% continuously with their formation, the filaments being maintained continuously under tension, the stretching of the filaments being initiated at a point not more than 60 cm. from the spinnerets and the final speed being not greater than 12 meters per minute.
  • a process for the production of filaments of high organisation and high tensile strength having a degree of polymerisation above 300 which comprises extruding through spinnerets a viscose of gamma number above 60, the cellulose generated from said viscose having a degree of polymerisation above 300, into an aqueous coagulating bath at room temperature containing only from 10-40 g./litre of sulphuric acid and at most 100 g./litre of sodium sulphate, and stretching the filaments about 240% during a period of 3 seconds at least continuously with their formation giving a final speed of 12 meters at most per minute, the filaments being maintained continuously under tension.

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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)
US301364A 1951-07-31 1952-07-28 Production by spinning of cellulose hydrate filaments Expired - Lifetime US2703270A (en)

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GB307931X 1951-07-31

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US (1) US2703270A (US07714131-20100511-C00024.png)
BE (1) BE513218A (US07714131-20100511-C00024.png)
CH (1) CH307931A (US07714131-20100511-C00024.png)
DE (1) DE1083016B (US07714131-20100511-C00024.png)
FR (1) FR1068692A (US07714131-20100511-C00024.png)
GB (1) GB720173A (US07714131-20100511-C00024.png)
NL (1) NL107330C (US07714131-20100511-C00024.png)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2860480A (en) * 1956-04-18 1958-11-18 Du Pont Regenerated cellulose structures and process for producing them
US3122820A (en) * 1958-05-30 1964-03-03 Watliff Company Ltd Method of manufacturing a rotor for a dynamo-electric machine
US3352957A (en) * 1962-11-06 1967-11-14 Chimiotex Process for spinning cellulosic fibers
DE1294590B (de) * 1962-05-16 1969-05-08 Toyo Spinning Co Ltd Verfahren zum Herstellen von Faeden oder Fasern aus regenerierter Cellulose
EP1245576A1 (en) * 1999-11-08 2002-10-02 Asahi Kasei Kabushiki Kaisha Cellulose dope and process for producing the same
US20140205830A1 (en) * 2011-06-21 2014-07-24 Lenzing Ag High strength cellulosic filament its use, and method for the production thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2422889A1 (fr) * 1978-04-14 1979-11-09 Commissariat Energie Atomique Soupape de regulation a declenchement automatique

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2413123A (en) * 1944-06-29 1946-12-24 Du Pont Production of rayon
US2607955A (en) * 1949-08-25 1952-08-26 Textile & Chem Res Co Ltd Spinning of viscose

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE572447C (de) * 1933-03-15 Spinnstofffabrik Zehlendorf G Verfahren zur Herstellung von Kunstseide
DE625352C (de) * 1932-03-18 1936-02-07 Algemeene Kunstzijde Unie N V Vorrichtung zum Strecken frisch gesponnener Kunstseidefaeden
DE609802C (de) * 1935-02-23 Steckborn Kunstseide A G Vorrichtung zur Herstellung von Viskosekunstseide unter Streckung
DE744891C (de) * 1938-10-22 1944-01-28 Ig Farbenindustrie Ag Verfahren zur Herstellung von Kunstseide, Fasern und Faeden aus Viscose
CH244571A (de) * 1943-12-16 1946-09-30 Haederli Charles Vorrichtung zur Streckung von künstlichen Fadengebilden, wie Einzelfäden, Bänder oder Kabel.

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2413123A (en) * 1944-06-29 1946-12-24 Du Pont Production of rayon
US2607955A (en) * 1949-08-25 1952-08-26 Textile & Chem Res Co Ltd Spinning of viscose

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2860480A (en) * 1956-04-18 1958-11-18 Du Pont Regenerated cellulose structures and process for producing them
US3122820A (en) * 1958-05-30 1964-03-03 Watliff Company Ltd Method of manufacturing a rotor for a dynamo-electric machine
DE1294590B (de) * 1962-05-16 1969-05-08 Toyo Spinning Co Ltd Verfahren zum Herstellen von Faeden oder Fasern aus regenerierter Cellulose
US3352957A (en) * 1962-11-06 1967-11-14 Chimiotex Process for spinning cellulosic fibers
EP1245576A1 (en) * 1999-11-08 2002-10-02 Asahi Kasei Kabushiki Kaisha Cellulose dope and process for producing the same
EP1245576A4 (en) * 1999-11-08 2004-05-19 Asahi Chemical Ind CELLULOSE SOLUTION AND METHOD FOR PRODUCING THE SAME
US7108907B1 (en) 1999-11-08 2006-09-19 Asahi Kasei Kabushiki Kaisha Cellulose dope and method for producing the same
US20140205830A1 (en) * 2011-06-21 2014-07-24 Lenzing Ag High strength cellulosic filament its use, and method for the production thereof

Also Published As

Publication number Publication date
CH307931A (de) 1955-06-30
FR1068692A (fr) 1954-06-30
NL107330C (US07714131-20100511-C00024.png)
GB720173A (en) 1954-12-15
BE513218A (US07714131-20100511-C00024.png)
DE1083016B (de) 1960-06-09

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