US3396528A - Permanentlay crimped, elastic chemically modified cotton yarns - Google Patents

Permanentlay crimped, elastic chemically modified cotton yarns Download PDF

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US3396528A
US3396528A US311934A US31193463A US3396528A US 3396528 A US3396528 A US 3396528A US 311934 A US311934 A US 311934A US 31193463 A US31193463 A US 31193463A US 3396528 A US3396528 A US 3396528A
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yarn
cotton
yarns
crimped
chemically modified
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Weiss Ernst
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Heberlein Patent Corp
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Heberlein Patent Corp
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G1/00Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
    • D02G1/02Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics by twisting, fixing the twist and backtwisting, i.e. by imparting false twist
    • D02G1/0286Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics by twisting, fixing the twist and backtwisting, i.e. by imparting false twist characterised by the use of certain filaments, fibres or yarns
    • D02G1/0293Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics by twisting, fixing the twist and backtwisting, i.e. by imparting false twist characterised by the use of certain filaments, fibres or yarns composed, at least in part, of natural fibres
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/345Nitriles
    • D06M13/348Nitriles unsaturated, e.g. acrylonitrile

Definitions

  • This invention relates to cotton yarns characterized by a permanent crimp and comparatively high elasticity, and also to methods for preparing such yarns.
  • Permanently crimped, torque or stretch yarns available today comprise continuous filament fully synthetic materials such as the polyamides and the polyesters. These products have achieved commercial significance for use principally in hosiery and the knitting arts and recently as weaving yarns. These stretch yarns are highly practical by reason of the permanent nature of the crimp which can easily be imparted to the fiber material. However, an appreciable number of individuals cannot tolerate direct epidermal contact with fully synthetic fabrics, and accordingly blending of the yarn with cotton or regenerated cellulose, which cellulosics are not irritating to the skin, has been necessary in many instances. It will be appreciated that permanently crimped yarns constructed entirely of cellulose or regenerated cellulose would be highly desirable and, by reason of the relatively high cost of polyester and polyamidic fibers, would also be economically very attractive.
  • the starting yarn in accordance with the present method is a cotton yarn which has been chemically modified.
  • chemically modified as employed in the specification and claims of this application shall be understood to mean cotton yarn which has been esterified and/or etherified to a hereinafter specified minimum extent or degree of substitution.
  • Such preferred chemical modifications include acetylation, cyanoethylation, benzylation and equivalent esterifications and etherifications set forth in the afore-mentioned Fisher application. Quite unexpectedly, slight esterification or etherification greatly increases the thermoplasticity of the fibers of the cotton yarn.
  • the starting chemically modified yarns herein are pref- 3,396,528 Patented Aug. 13, 1968 erably acetylated cotton of a degree of substitution of at least about 1.0, cyanoethylated cotton of a degree of substitution of at least about 0.4, or benzylated cotton of a degree of substitution of at least about 0.2.
  • Degree of substitution refers to the number of OH groups per glucose unit of the cellulose molecule which have been esterified or etherified.
  • the aforementioned minimum degree of substitution is essential in order to impart sufficient thermoplasticity to the cotton yarn to enable permanent crimping in accordance with the present method and to assure an elasticity in the crimped yarn product equal to at least about 10%, which may be considered to be about a practical minimum in permanently crimped elastic yarns.
  • the chemically modified yarn substantially retain its individual fiber structure, and accordingly the extent of chemical modification must not be such as would appreciably destroy the fiber structure of the formed yarn. It is possible, for example, by the use of low temperature esterification and the exercise of extreme care to acetylate cotton cellulose to a degree of substitution of 3.0 with retention of fibrous character.
  • Such highly substituted yarns are suitable for the purpose of this invention as long as fibrous character of the cellulose is retained after chemical modification.
  • Acetylation A cotton hank roving is wound onto a stainless steel dye tube, pretreated for seventeen hours in a solution containing 99% acetic acid and 1% water. The solution is then drained and the dye tube and cotton roving are immersed in a liquid consisting of 54.75% acetic anhydride, isopropyl acetate and 0.25% perchloric acid, where it is allowed to remain for one hour and forty-five minutes at a temperature of 15 C. Following this treatment the acetyl content of the cotton roving is found to be 35.8% by weight, which is equal to a degree of substitution of about 1.5. This is considered a higher acetylated product.
  • a lower acetyl cotton may be prepared by pre-soaking a cotton yarn for about 2 hours at C. in glacial acetic acid, draining and then reacting for about 1 /2 hours in 25% acetic anhydride, 74.85% acetic acid and 0.15% perchloric acid at about 20 C. The yarn is then drained, washed in tap water and finally at a temperature of about C. The acetyl content of the modified cotton yarn thus produced is between about 23 and 28%.
  • Benzylation A cotton yarn is wound onto a stainless steel perforated dye tube under very light tension and then saturated with an aqueous caustic soda solution containing 30% NaOH and 1% ethylene glycol by weight.
  • the solution is circulated from the inside to the outside of the package for approximately thirty minutes at about 30 C., then drained off and the package extracted by blowing air through it from the inside out.
  • the benzylation reaction is then carried out by immersing the package in circulating pure benzyl chloride at a temperature of C. After the desired reaction time the solution is cooled to room temperature, drained and the package is again extracted with air, washed with water at about 60 C. approximately thirty minutes then with a synthetic detergent for approximately thirty minutes and finally again with hot water.
  • the desired degree of substitution is dependent upon the reaction time.
  • the optimum reaction is the point when the flow rate from the inside-out, which will increase steadily to a maximum and then decrease steadily, reaches the same value that was obtained when the reaction was started.
  • the nitrogen content of the thus modified cotton yarn is about 4-5
  • a cotton yarn which has been chemically modified to increase its thermoplasticity is subjected to high twisting and heat fixation or setting in the highly twisted condition during which treatment the filaments of the yarn exhibit a plastic deformation as a result of high twisting.
  • the yarn is untwisted to substantially the same extent that it was initially high twisted; thereby interior torsional tensions are created which are suflicient for the formation of a yarn having a permanent crimp.
  • the treatment thus constitutes a temporary high twisting of the yarn which is preferably accomplished by means of a false twisting device, a variety of which are well known in the art.
  • the yarn coming from the supply roll passes in succession through a first conveyor, for example a pair of rollers, through a heater or over a heated element, then through the twist imparter of the apparatus, through a second conveyor which again may be a pair of rollers, and finally to take-up or winding device.
  • a first conveyor for example a pair of rollers
  • a heater or over a heated element then through the twist imparter of the apparatus, through a second conveyor which again may be a pair of rollers, and finally to take-up or winding device.
  • the heating device may comprise a tube through which the yarn passes in axial direction and which is provided with an electrical resistance heating coil.
  • a box may be used with several heating coils for simultaneous passage of separate yarns at different points.
  • heat setting of the highly twisted yarn may be accomplished by contact with a heated surface, preferably a metal surface which has been brought to the required temperature electrically.
  • the temperature employed for heating the yarn depends upon the nature of the cotton fiber material and the thickness of the yarn. Excellent results are obtained with yarns of English numbers to 100 when subjected in highly twisted condition to setting temperatures ranging from about 200 to about 280 C. with the time the yarn is subjected to these elevated temperatures being at least about 0.2 second and preferably between about 0.5 and 5 seconds. It will be appreciated that the coarser the yarn the longer the setting time or the higher the temperature to which the yarn is subjected, with temperature and time being thus inter-related.
  • false twisting and heat setting may be carried out with a single end yarn, in which case the direction of temporary high twisting is the same as the direction of the spinning twist of the yarn so that the staple yarn will not pass through a point of zero twist and thus disintegrate.
  • two single end yarns similarly but separately false twisted and heat-set by high twisting in one direction may then be doubled and ply-twisted in the opposite direction to produce a two-ply crimped yarn.
  • two single yarns each with an original spinning twist of 500 turns/ meter Z may be separately false twisted in Z-direction and heat-set after which each remains at its original 500 turns/meter Z.
  • These yarns may then be plied in S- direction, for example with about 450 turns/meter S, that is near to the zero point, to produce a two-ply, rather open, voluminous permanently crimped yarn.
  • the yarns as a rule are given a permanent ply twist in a direction opposite to the direction of its spinning twist.
  • the ends of chemically modified cotton yarn will generally be similarly constructed yarns, i.e. of equivalent English yarn numbers and of substantially equivalent twistconstants.
  • two yarns with a spinning twist in Z-direction may be temporarily highly twisted by means of a false twisting device in S-direction past the zero point and thereupon permanently ply-twisted in S-direction.
  • a false twisting device in S-direction past the zero point and thereupon permanently ply-twisted in S-direction.
  • the plying twist imparted in the final step of the method may range from about to 500 turns/meter and is as a rule in a direction opposite to the direction of the spinning twist of the starting yarn.
  • a ply twist up to about 500 turns/meter may be imparted to two or more yarns in cases where a very close, i.e. non-voluminous, stretch yarn is desired. However, in most instances a voluminous, permanently crimped elastic yarn will be plied to only about 100 to 300 turns/meter.
  • the crimped yarns of this invention may thus be voluminous or rather close, but in either event they have an attractive and full silky feel and excellent covering capacity as compared with the uncrimped starting chemically modified yarn or with conventional unmodified cotton yarns.
  • the yarn products hereof further exhibit a relatively great absorptive capacity as compared with fully synthetic yarns of the aforementioned types, which is an important, advantageous physiological property.
  • the yarn products hereof are also permanently crimped and have an elasticity greater than about 10%, and generally between about 10 and 40%.
  • the best test for determining permanence of the crimp is repeated launderings at elevated temperature to simulate conditions encountered in actual use of fabrics constructed of the yarns of the present invention. These tests are as follows: The crimp may be considered permanent if the crimp contraction is not substantially diminished after a laundering in a solution containing 5 g. of soap per liter at elevated temperature.
  • EXAMPLE 1 Two acetylated cotton yarns with an acetyl content of 36% corresponding to a degree of substitution of 1.5, each of English yarn number and of twist constant equal to 2.5, i.e., a spinning twist of about 600 turns/ meter in Z-direction, were temporarily highly twisted together in a false twisting device to 2100 turns/meter S and heated in the highly twisted condition for a period of 4.1 seconds in a hot air chamber at 240 C. The two yarns were then finally plied and twisted to 240 turns/ meter S.
  • the product was a typically crimped relatively voluminous two-ply yarn having an elasticity or crimp contraction equal to about 21%.
  • the crimp in the yarn should first be fully developed. Five skeins, each being 8 times the circumference of the reel on which they are wound (preferably 8 meters or yards), should be reeled off the cross-wound packages. The tension of the yarn during reeling off should be so controlled that v tion with 1.8 g./tex. Care should be taken to ensure that skeins are completely smooth when suspended. After the load has been applied for 1 minute, the length of the wet, stretched skeins is measured. The weights are then removed and the skeins are dried at -60" C. freely suspended and without any loading.
  • a strand of the yarn was subjected to a boiling laundering in a solution containing 5 g. of soap per liter. After this laundering the crimp contraction was not substantially reduced. This shows that the crimp of the yarn is permanent.
  • EXAMPLE 2 Three benzylated cotton yarns of a degree of substitution of 0.45 each of English yarn number 60 and a spinning twist in Z direction equal to a twist constant of 3.9 were led together through a false twisting device, temporarily highly twisted to 2000 turns/meter S and heated in the highly twisted condition for 4 seconds at 240 C. Following untwisting the three yarns were plytwisted to 300 turns/meter S. The three-ply yarn thus obtained was found to be substantially more voluminous than a similar three-ply yarn of untreated cotton, and had an elasticity of 10.8%. A strand of the yarn was subjected to laundering at 60 C. in a solution of 5 g. of soap per liter, whereby the crimp contraction was not substantially reduced. This shows that the crimp of the yarn is permanent.
  • EXAMPLE 3 Two cyanoethylated cotton yarns containing 3.5% nitrogen, corresponding to a degree of substitution of 0.45 each of English yarn number 10 and a spinning twist in Z direction equal to a twist constant of 3 were temporarily highly twisted together on a false twisting apparatus to 1100 turns/meter S and exposed in the highly twisted condition for 2 seconds to heated air at 270 C. Subsequently the yarns were ply-twisted to turns/meter S to produce a two-ply yarn with a full hand. A strand of the yarn was then washed as described in Example 1 whereby the crimp contraction remained practically unchanged.
  • EXAMPLE 4 Four acetylated cotton yarns with an acetyl content of about 3040% each of English yarn number 100 and a spinning twist in Z direction equal to a twist constant of 3 were temporarily highly twisted together on a false twisting device to 2500 turns/ meter S and while in highly twisted condition passed over a heated metal surface which was maintained at about 250 C. The yarns were in contact with the heated surface for approximately three seconds. Subsequently the four yarns were plytwisted to 250 turns/meter S. The four-ply yarn thus produced was voluminous, had a full hand, a crimp contraction which is very substantially greater than an analogous four-ply unmodified cotton yarn. A strand of yarn was then washed as described in Example 1, whereby the crimp contraction remained practically unchanged.
  • EXAMPLE 5 Two single end yarns of acetylated cotton with an acetyl content of about 30-40% each of English yarn number 50 and an original spinning twist of 500 turns/meter Z are separately temporarily highly twisted in a false twisting device to 2000 turns/meter Z and heated in .the highly twisted condition for 2 seconds in a hot air chamber at 270 C. The two yarns are then ply-twisted in S-direction with 300 turns/meter S. The product is 'a rather open, voluminous permanently crimped twoply yarn. A strand of the yarn was then washed as described in Example 1 whereby the crimp contraction was not substantially diminished. v
  • EXAMPLE 6 Two unmodified cotton yarns, each of English yarn number 40, and a twist constant equal to 2.5, spinning twist in Z direction, were plied and temporarily highly twisted to 2100 turns per meter S, and heated in the highly twisted condition for a period of 4.1 seconds in a hot air chamber at 240 C. Thereafter the two yarns were ply-twisted to 240 turns per meter S direction. The product thus obtained was practically not crimped.
  • chemically modified as employed in the appended claims is intended to mean only cotton yarn which has been either esterified or etherified by acetylation, benzylation or cyanoethylation to a minimum degree of substitution of at least about 1.0, 0.2 and 0.4, respectively, with the degree of substitution in each instance being less than that which would destroy the fibrous character of the cotton.
  • a stretchable fabric constructed of permanently crimped chemically modified cotton yarn of the group consisting of acetylated cotton yarn of a degree of substitution of at least about 1, cyanoethylated cotton yarn of a degree of substitution of at least about 0.4 and benzylated cotton yarn of a degree of substitution of at least about 0.2, the degree of substitution in each instance being less than that which would destroy the fibrous character of the cotton, said yarns having an elasticity of at least about 10%.

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  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)

Description

United States 3,396,528 PERMANENTLY CRIMPED, ELASTIC CHEMICAL- LY MODIFIED COTTON YARNS Ernst Weiss, Wattwil, Switzerland, assignor to Heheriein Patent Corporation, New York, N.Y., a corporation of New York No Drawing. Original application June 21, 1962, Ser. No. 204,079. Divided and this application Sept. 12, 1963, Ser. No. 311,934
11 Claims. (Cl. 57-139) This application is a division of US. patent application S.N. 204,079, filed June 21, 1962.
This invention relates to cotton yarns characterized by a permanent crimp and comparatively high elasticity, and also to methods for preparing such yarns.
Permanently crimped, torque or stretch yarns available today comprise continuous filament fully synthetic materials such as the polyamides and the polyesters. These products have achieved commercial significance for use principally in hosiery and the knitting arts and recently as weaving yarns. These stretch yarns are highly practical by reason of the permanent nature of the crimp which can easily be imparted to the fiber material. However, an appreciable number of individuals cannot tolerate direct epidermal contact with fully synthetic fabrics, and accordingly blending of the yarn with cotton or regenerated cellulose, which cellulosics are not irritating to the skin, has been necessary in many instances. It will be appreciated that permanently crimped yarns constructed entirely of cellulose or regenerated cellulose would be highly desirable and, by reason of the relatively high cost of polyester and polyamidic fibers, would also be economically very attractive.
Unfortunately, ordinary cotton possesses only very limited thermoplasticity, and accordingly it is impossible to impart any useful crimp to cotton yarns. Techniques for producing permanently crimped or torque stretch nylon yarns, for example, are without effect upon cotton yarn. In fact, the high twisting, heat-setting and subsequent detwisting employed in the production of crimped polyamide yarns produce no useful modification of the physical properties of a cotton yarn simply because cotton has no memory, i.e., is practically not thermoplastic.
Through recent work of Dr. C. H. Fisher at the Southern Regional Research Laboratory of the United States Department of Agriculture chemically modified cotton yarns have been developed which possess appreciable thermoplasticity and which have very favorable textile properties. For a further description of this chemically modified cotton yarn and its method of production reference may be had to Fisher U.S. patent application Ser. No. 204,299, filed on June 21, 1962, now abandoned.
It is among the objects of the present invention to produce a novel permanently crimped cotton yarn which has been modified chemically as set forth hereinafter, and to provide methods for permanently crimping such yarns.
The starting yarn in accordance with the present method is a cotton yarn which has been chemically modified. The term chemically modified as employed in the specification and claims of this application shall be understood to mean cotton yarn which has been esterified and/or etherified to a hereinafter specified minimum extent or degree of substitution. Such preferred chemical modifications include acetylation, cyanoethylation, benzylation and equivalent esterifications and etherifications set forth in the afore-mentioned Fisher application. Quite unexpectedly, slight esterification or etherification greatly increases the thermoplasticity of the fibers of the cotton yarn.
The starting chemically modified yarns herein are pref- 3,396,528 Patented Aug. 13, 1968 erably acetylated cotton of a degree of substitution of at least about 1.0, cyanoethylated cotton of a degree of substitution of at least about 0.4, or benzylated cotton of a degree of substitution of at least about 0.2. Degree of substitution refers to the number of OH groups per glucose unit of the cellulose molecule which have been esterified or etherified. The aforementioned minimum degree of substitution is essential in order to impart sufficient thermoplasticity to the cotton yarn to enable permanent crimping in accordance with the present method and to assure an elasticity in the crimped yarn product equal to at least about 10%, which may be considered to be about a practical minimum in permanently crimped elastic yarns. It is important, of course, that the chemically modified yarn substantially retain its individual fiber structure, and accordingly the extent of chemical modification must not be such as would appreciably destroy the fiber structure of the formed yarn. It is possible, for example, by the use of low temperature esterification and the exercise of extreme care to acetylate cotton cellulose to a degree of substitution of 3.0 with retention of fibrous character. Such highly substituted yarns are suitable for the purpose of this invention as long as fibrous character of the cellulose is retained after chemical modification.
Typical methods for chemically modifying the cotton yarn, while not forming a part of the present invention, are as follows:
Acetylation A cotton hank roving is wound onto a stainless steel dye tube, pretreated for seventeen hours in a solution containing 99% acetic acid and 1% water. The solution is then drained and the dye tube and cotton roving are immersed in a liquid consisting of 54.75% acetic anhydride, isopropyl acetate and 0.25% perchloric acid, where it is allowed to remain for one hour and forty-five minutes at a temperature of 15 C. Following this treatment the acetyl content of the cotton roving is found to be 35.8% by weight, which is equal to a degree of substitution of about 1.5. This is considered a higher acetylated product. A lower acetyl cotton may be prepared by pre-soaking a cotton yarn for about 2 hours at C. in glacial acetic acid, draining and then reacting for about 1 /2 hours in 25% acetic anhydride, 74.85% acetic acid and 0.15% perchloric acid at about 20 C. The yarn is then drained, washed in tap water and finally at a temperature of about C. The acetyl content of the modified cotton yarn thus produced is between about 23 and 28%.
Benzylation A cotton yarn is wound onto a stainless steel perforated dye tube under very light tension and then saturated with an aqueous caustic soda solution containing 30% NaOH and 1% ethylene glycol by weight. The solution is circulated from the inside to the outside of the package for approximately thirty minutes at about 30 C., then drained off and the package extracted by blowing air through it from the inside out. The benzylation reaction is then carried out by immersing the package in circulating pure benzyl chloride at a temperature of C. After the desired reaction time the solution is cooled to room temperature, drained and the package is again extracted with air, washed with water at about 60 C. approximately thirty minutes then with a synthetic detergent for approximately thirty minutes and finally again with hot water. The desired degree of substitution is dependent upon the reaction time. The optimum reaction is the point when the flow rate from the inside-out, which will increase steadily to a maximum and then decrease steadily, reaches the same value that was obtained when the reaction was started.
3 Cyanoethylation Cotton yarn is thoroughly wetted out with a 2% by weight sodium hydroxide solution after which it is centirfuged to approximately 70% wet take-up. The yarn is then reacted in water-saturated acrylonitrile at 65 C. for about thirty to forty-five minutes, whereupon the solution is drained oif and the yarn carefully washed in an aqueous solution containing 1% phosphoric acid. The yarn is again drained and washed with tap water until all reagents are removed. The nitrogen content of the thus modified cotton yarn is about 4-5 In accordance with the method of the present invention a cotton yarn which has been chemically modified to increase its thermoplasticity is subjected to high twisting and heat fixation or setting in the highly twisted condition during which treatment the filaments of the yarn exhibit a plastic deformation as a result of high twisting. Following high twisting and setting the yarn is untwisted to substantially the same extent that it was initially high twisted; thereby interior torsional tensions are created which are suflicient for the formation of a yarn having a permanent crimp. The treatment thus constitutes a temporary high twisting of the yarn which is preferably accomplished by means of a false twisting device, a variety of which are well known in the art. In such devices the yarn coming from the supply roll passes in succession through a first conveyor, for example a pair of rollers, through a heater or over a heated element, then through the twist imparter of the apparatus, through a second conveyor which again may be a pair of rollers, and finally to take-up or winding device.
The heating device may comprise a tube through which the yarn passes in axial direction and which is provided with an electrical resistance heating coil. Instead of a tube, a box may be used with several heating coils for simultaneous passage of separate yarns at different points. Also, heat setting of the highly twisted yarn may be accomplished by contact with a heated surface, preferably a metal surface which has been brought to the required temperature electrically.
In accordance with the present invention the temperature employed for heating the yarn depends upon the nature of the cotton fiber material and the thickness of the yarn. Excellent results are obtained with yarns of English numbers to 100 when subjected in highly twisted condition to setting temperatures ranging from about 200 to about 280 C. with the time the yarn is subjected to these elevated temperatures being at least about 0.2 second and preferably between about 0.5 and 5 seconds. It will be appreciated that the coarser the yarn the longer the setting time or the higher the temperature to which the yarn is subjected, with temperature and time being thus inter-related.
Further in accordance with the present invention chemically modified cotton yarns are used which have a low degree of spinning twist corresponding to a twist constant preferably between about 1.5 and 3 and not above a maximum of 4. The twist constant A is calculated in accordance with the formula: A=T/ /Ne, where T is the number of turns per English inch and Ne is the English yarn number.
According to one embodiment of the present method, false twisting and heat setting may be carried out with a single end yarn, in which case the direction of temporary high twisting is the same as the direction of the spinning twist of the yarn so that the staple yarn will not pass through a point of zero twist and thus disintegrate. In this embodiment two single end yarns similarly but separately false twisted and heat-set by high twisting in one direction, for example, may then be doubled and ply-twisted in the opposite direction to produce a two-ply crimped yarn. For example two single yarns each with an original spinning twist of 500 turns/ meter Z may be separately false twisted in Z-direction and heat-set after which each remains at its original 500 turns/meter Z. These yarns may then be plied in S- direction, for example with about 450 turns/meter S, that is near to the zero point, to produce a two-ply, rather open, voluminous permanently crimped yarn. Following temporary high twisting and heat-setting the yarns as a rule are given a permanent ply twist in a direction opposite to the direction of its spinning twist. Furthermore it is often of advantage, to simultaneously hightwist at least two ends of yarn; the ends of chemically modified cotton yarn will generally be similarly constructed yarns, i.e. of equivalent English yarn numbers and of substantially equivalent twistconstants. Thus, for example, two yarns with a spinning twist in Z-direction may be temporarily highly twisted by means of a false twisting device in S-direction past the zero point and thereupon permanently ply-twisted in S-direction. As a result of the simultaneous temporary high twisting of at least two yarns, disintegration and/or undesired loosening of the single ends during passage through the zero point is avoided by wrapping of one ply about the other. The final two-ply crimped yarn thus produced possesses a decreased tendency toward distortion and is a relatively open and voluminous yarn.
In accordance with the present invention the plying twist imparted in the final step of the method may range from about to 500 turns/meter and is as a rule in a direction opposite to the direction of the spinning twist of the starting yarn. The higher the number of ply twist per unit length the closer or tighter will be the filaments of the product. A ply twist up to about 500 turns/meter may be imparted to two or more yarns in cases where a very close, i.e. non-voluminous, stretch yarn is desired. However, in most instances a voluminous, permanently crimped elastic yarn will be plied to only about 100 to 300 turns/meter.
The crimped yarns of this invention may thus be voluminous or rather close, but in either event they have an attractive and full silky feel and excellent covering capacity as compared with the uncrimped starting chemically modified yarn or with conventional unmodified cotton yarns. The yarn products hereof further exhibit a relatively great absorptive capacity as compared with fully synthetic yarns of the aforementioned types, which is an important, advantageous physiological property.
The yarn products hereof are also permanently crimped and have an elasticity greater than about 10%, and generally between about 10 and 40%. Elasticity as expressed in percent, often referred to as crimp contraction is determined in accordance with the formula where a is the length of a strand of yarn wetted with water and measured while under a stress of 1.8 g./tex. and b is the length of the same strand after it has been dried in a controlled atmosphere in unstressed condition and then subjected to a stress of 0.018 g./tex. (tex.=grams per 1000 meters).
The best test for determining permanence of the crimp is repeated launderings at elevated temperature to simulate conditions encountered in actual use of fabrics constructed of the yarns of the present invention. These tests are as follows: The crimp may be considered permanent if the crimp contraction is not substantially diminished after a laundering in a solution containing 5 g. of soap per liter at elevated temperature.
The present invention will be further apparent from the following non-limiting examples which illustrate typical methods and products thereof as presently practiced. One of these examples also serves to compare the yarns of the invention with unmodified cotton yarn which have been processed in accordance herewith.
EXAMPLE 1 Two acetylated cotton yarns with an acetyl content of 36% corresponding to a degree of substitution of 1.5, each of English yarn number and of twist constant equal to 2.5, i.e., a spinning twist of about 600 turns/ meter in Z-direction, were temporarily highly twisted together in a false twisting device to 2100 turns/meter S and heated in the highly twisted condition for a period of 4.1 seconds in a hot air chamber at 240 C. The two yarns were then finally plied and twisted to 240 turns/ meter S. The product was a typically crimped relatively voluminous two-ply yarn having an elasticity or crimp contraction equal to about 21%.
Before crimp contraction is determined, the crimp in the yarn should first be fully developed. Five skeins, each being 8 times the circumference of the reel on which they are wound (preferably 8 meters or yards), should be reeled off the cross-wound packages. The tension of the yarn during reeling off should be so controlled that v tion with 1.8 g./tex. Care should be taken to ensure that skeins are completely smooth when suspended. After the load has been applied for 1 minute, the length of the wet, stretched skeins is measured. The weights are then removed and the skeins are dried at -60" C. freely suspended and without any loading. After cooling down for 1 hour in a conditioned room (temperature 20 C., relative humidity the freely suspended skeins are loaded with 0.018 g./teX. After this load has been applied for 1 minute the length of the skeins is measured. On the basis of these measurements the average crimp contraction was calculated by the aforementioned formula.
A strand of the yarn was subjected to a boiling laundering in a solution containing 5 g. of soap per liter. After this laundering the crimp contraction was not substantially reduced. This shows that the crimp of the yarn is permanent.
EXAMPLE 2 Three benzylated cotton yarns of a degree of substitution of 0.45 each of English yarn number 60 and a spinning twist in Z direction equal to a twist constant of 3.9 were led together through a false twisting device, temporarily highly twisted to 2000 turns/meter S and heated in the highly twisted condition for 4 seconds at 240 C. Following untwisting the three yarns were plytwisted to 300 turns/meter S. The three-ply yarn thus obtained was found to be substantially more voluminous than a similar three-ply yarn of untreated cotton, and had an elasticity of 10.8%. A strand of the yarn was subjected to laundering at 60 C. in a solution of 5 g. of soap per liter, whereby the crimp contraction was not substantially reduced. This shows that the crimp of the yarn is permanent.
EXAMPLE 3 Two cyanoethylated cotton yarns containing 3.5% nitrogen, corresponding to a degree of substitution of 0.45 each of English yarn number 10 and a spinning twist in Z direction equal to a twist constant of 3 were temporarily highly twisted together on a false twisting apparatus to 1100 turns/meter S and exposed in the highly twisted condition for 2 seconds to heated air at 270 C. Subsequently the yarns were ply-twisted to turns/meter S to produce a two-ply yarn with a full hand. A strand of the yarn was then washed as described in Example 1 whereby the crimp contraction remained practically unchanged.
EXAMPLE 4 Four acetylated cotton yarns with an acetyl content of about 3040% each of English yarn number 100 and a spinning twist in Z direction equal to a twist constant of 3 were temporarily highly twisted together on a false twisting device to 2500 turns/ meter S and while in highly twisted condition passed over a heated metal surface which was maintained at about 250 C. The yarns were in contact with the heated surface for approximately three seconds. Subsequently the four yarns were plytwisted to 250 turns/meter S. The four-ply yarn thus produced was voluminous, had a full hand, a crimp contraction which is very substantially greater than an analogous four-ply unmodified cotton yarn. A strand of yarn was then washed as described in Example 1, whereby the crimp contraction remained practically unchanged.
EXAMPLE 5 Two single end yarns of acetylated cotton with an acetyl content of about 30-40% each of English yarn number 50 and an original spinning twist of 500 turns/meter Z are separately temporarily highly twisted in a false twisting device to 2000 turns/meter Z and heated in .the highly twisted condition for 2 seconds in a hot air chamber at 270 C. The two yarns are then ply-twisted in S-direction with 300 turns/meter S. The product is 'a rather open, voluminous permanently crimped twoply yarn. A strand of the yarn was then washed as described in Example 1 whereby the crimp contraction was not substantially diminished. v
EXAMPLE 6 Two unmodified cotton yarns, each of English yarn number 40, and a twist constant equal to 2.5, spinning twist in Z direction, were plied and temporarily highly twisted to 2100 turns per meter S, and heated in the highly twisted condition for a period of 4.1 seconds in a hot air chamber at 240 C. Thereafter the two yarns were ply-twisted to 240 turns per meter S direction. The product thus obtained was practically not crimped.
As noted hereinabove, chemically modified as employed in the appended claims is intended to mean only cotton yarn which has been either esterified or etherified by acetylation, benzylation or cyanoethylation to a minimum degree of substitution of at least about 1.0, 0.2 and 0.4, respectively, with the degree of substitution in each instance being less than that which would destroy the fibrous character of the cotton.
I claim:
1. Permanently crimped, elastic chemically modified cotton yarn, said cotton yarn being etherified or esterified by acetylation, benzylation, or cyanoethylation.
2. Permanently crimped, elastic chemically modified cotton yarn, said cotton yarn being etherified or esterified by acetylation, benzylation or cyanoethylation and havirag an English yarn number between about 10 and about 1 0.
3. Permanently crimped, chemically modified cotton yarn, said cotton yarn being etherified or esterified by acetylation, benzylation, or cyanoethylation and having elasticity equal to at least about 10%.
4. Permanently crimped, chemically modified cotton yarn, said cotton yarn being etherified or esterified by acetylation, benzylation, or cyanoethylation and having elasticity between about 10 and 30%.
5. Permanently crimped, elastic chemically modified cotton multi-ply yarn, said cotton yarn being etherified or esterified by acetylation, benzylation, or cyanoethylation and the ply ends of which are of English yarn number between about 10 and 100, having a ply-twist between about 100 and 500 turns/ meter.
6. Permanently crimped, elastic chemically modified cotton multi-ply yarn, said cotton yarn being etherified or esterified by acetylation, benzylation, or cyanoethylation and having a ply-twist between about 100 and 500 turns/meter, the single ends of which have a spinning twist constant of less than about 4 and are of English yarn number between about 10 and 100.
7. A permanently crimped, voluminous elastic yarn as set forth in claim 6 wherein the ply-twist is between about 100 and 300 turns/meter.
8. Permanently crimped acetylated cotton yarn of a degree of substitution of at least about 1 and an elasticity of at least about 10%, the degree of substitution being less than that which would destroy the fibrous character of the cotton.
9. Permanently crimped cyanoethylated cotton yarn of a degree of substitution of at least about 0.4 and an elasticity of at least about 10%, the degree of substitution being less than that which would destroy the fibrous character of the cotton.
10. Permanently crimped benzylated cotton yarn of a degree of substitution of at least about 0.2 and an elasticity of at least about 10%, the degree of substitution being less than that which would destroy the fibrous character of the cotton.
11. A stretchable fabric constructed of permanently crimped chemically modified cotton yarn of the group consisting of acetylated cotton yarn of a degree of substitution of at least about 1, cyanoethylated cotton yarn of a degree of substitution of at least about 0.4 and benzylated cotton yarn of a degree of substitution of at least about 0.2, the degree of substitution in each instance being less than that which would destroy the fibrous character of the cotton, said yarns having an elasticity of at least about 10%.
References Cited OTHER REFERENCES Conrad: Mechanical Behavior of cyanoethylated Cotton Textiles, Textile Research Journal, vol. 29, No. 4, April 1959.
Conrad: Changes in Fine Structure and Mechanical Properties Induced by Cyanoethylation of Cotton Yarns, Textile Research Journal, vol. 30, N0. 5, May 1960.
JOHN PETRAKES, Primary Examiner.

Claims (1)

1. PERMANENTLY CRIMPED, ELASTIC CHEMICALLY MODIFIED COTTON YARN, SAID COTTON YARN BEING ETHERIFIED OR ESTERIFIED BY ACETYLATION, BENZYLATION, OR CYANOETHYLATION.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4418524A (en) * 1980-06-19 1983-12-06 Kao Soap Co., Ltd. Twisted yarn and twisted bundle of yarns

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US1800944A (en) * 1924-05-30 1931-04-14 Lilienfeld Leon Process for improving vegetable textile material
GB478259A (en) * 1936-07-16 1938-01-17 Henry Dreyfus Improvements in the manufacture of cellulose derivatives
US2463618A (en) * 1943-10-18 1949-03-08 Heberlein Patent Corp Process for producing fibrous material and the product
US2980491A (en) * 1955-06-15 1961-04-18 Segal Leon Textile fibers comprising perfluoroalkanoyl esters of cellulose and process of making the same
US2993749A (en) * 1958-05-23 1961-07-25 William G Sloan Cellulose esters with dimensional stability
US3025659A (en) * 1955-02-21 1962-03-20 Leesona Corp Method of thermally processing non-thermoplastic yarn
US3037902A (en) * 1960-12-22 1962-06-05 Rayonier Inc Partial acetylation of cellulose
AU665131B2 (en) * 1992-12-04 1995-12-14 Sony Corporation Method for recording and reproducing digital signal

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Publication number Priority date Publication date Assignee Title
US1800944A (en) * 1924-05-30 1931-04-14 Lilienfeld Leon Process for improving vegetable textile material
GB478259A (en) * 1936-07-16 1938-01-17 Henry Dreyfus Improvements in the manufacture of cellulose derivatives
US2463618A (en) * 1943-10-18 1949-03-08 Heberlein Patent Corp Process for producing fibrous material and the product
US3025659A (en) * 1955-02-21 1962-03-20 Leesona Corp Method of thermally processing non-thermoplastic yarn
US2980491A (en) * 1955-06-15 1961-04-18 Segal Leon Textile fibers comprising perfluoroalkanoyl esters of cellulose and process of making the same
US2993749A (en) * 1958-05-23 1961-07-25 William G Sloan Cellulose esters with dimensional stability
US3037902A (en) * 1960-12-22 1962-06-05 Rayonier Inc Partial acetylation of cellulose
AU665131B2 (en) * 1992-12-04 1995-12-14 Sony Corporation Method for recording and reproducing digital signal

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4418524A (en) * 1980-06-19 1983-12-06 Kao Soap Co., Ltd. Twisted yarn and twisted bundle of yarns

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