US2989797A - Process for the manufacture of staple yarns by filament decomposition - Google Patents
Process for the manufacture of staple yarns by filament decomposition Download PDFInfo
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- US2989797A US2989797A US624207A US62420756A US2989797A US 2989797 A US2989797 A US 2989797A US 624207 A US624207 A US 624207A US 62420756 A US62420756 A US 62420756A US 2989797 A US2989797 A US 2989797A
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- fibres
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- decomposition
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- 238000000034 method Methods 0.000 title claims description 23
- 238000000354 decomposition reaction Methods 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- -1 POLYETHYLENE TEREPHTHALATE Polymers 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 4
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 4
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 claims description 4
- 229950006389 thiodiglycol Drugs 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 239000000835 fiber Substances 0.000 description 18
- 239000000126 substance Substances 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 8
- 238000005520 cutting process Methods 0.000 description 7
- 238000009987 spinning Methods 0.000 description 7
- 239000004753 textile Substances 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 230000001788 irregular Effects 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 1
- 229960002327 chloral hydrate Drugs 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01G—PRELIMINARY TREATMENT OF FIBRES, e.g. FOR SPINNING
- D01G1/00—Severing continuous filaments or long fibres, e.g. stapling
- D01G1/02—Severing continuous filaments or long fibres, e.g. stapling to form staple fibres not delivered in strand form
- D01G1/022—Severing continuous filaments or long fibres, e.g. stapling to form staple fibres not delivered in strand form by solvents
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/04—Polyester fibers
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/10—Polyvinyl halide esters or alcohol fiber modification
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/21—Nylon
Definitions
- Filaments and fabrics consisting of such fibres show a very silky character, but not the full and warming handle of textile goods consisting of shortstapled fibrous material, as, for instance, wool or cotton. For this reason it is necessary to decompose the continuous filaments by means of cutting devices in order to obtain short fibres showing spinning properties and allowing of variations of length, for instance from 20 to 250 mm.
- fibres of a high swelling capacity for instance fibres of cellulose or protein regeneration prod ucts
- the cutting can be performed very easily when the fibres are wet.
- completely synthetic fibres eg those belonging to the polyamide, polyacryl and polyester series
- the process of forming staples gives rise to a considerable consumption of energy and in increased abrasion of the knives.
- the decomposition into short fibres shows the drawback that the single filaments arranged in parallel and leaving the spinning nozzles become snarled in the course of the cutting and finishing processes so that they have to be subjected to the same process in order to secure their parallel arrangement in the spinning process, as is necessary with natural fibres. Also the losses of fibres occurring during cutting and the following run over the carding machines represent a perceptible economical factor.
- the cutting process causes a rapid abrasion of the knives, thereby diminishing the capacity of the machines and, due to unsharp cutting or tearing, also injuriously affecting the quality of the staple.
- fibres showing spinning properties by applying onto bundles, cables or slivers of endless filaments, chemical compounds in the form of small stripes by means of patterns, rollers and the like, thereby damaging or destroying the fibres.
- This is to be done in such a way that the distance between one spot of application and the next one corresponds to the length of staple required.
- the material to be treated is to be subjected to such conditions that local breaks of the fibre substance sufficient for the decomposition of the continuous filament, take place.
- the method of the invention is illustrated in the accompanying drawing, which shows a bundle of endless filaments having a decomposing agent applied to the filaments in the form of a stripe.
- the present invention is to be distinguished from that described and claimed in copending application Serial No. 598,741, filed July 19, 1956, by Niisslein et al.
- the invention of the copending application relates to the selective printing of fabrics with decomposing agents, and not the use of such agents on fibers adaptable to subsequent fashioning into fabrics.
- the chemical compounds to be chosen in each case depend upon the chemical nature of the fibrous substance.
- cellulose regeneration fibres can be destroyed by means of substances showing an acid reaction
- protein regeneration fibres can be destroyed by means of substances showing an alkaline reaction.
- superpolyamide fibres are affected by strong mineral acids, acid amides, or aqueous chloral hydrate solution of 70% strength.
- polyester fibres excellent results can be attained with highly concentrated mineral acids as well as with several bases, especially with guanidine carbonate in connection with glycol, glycol derivatives, quarternary ammonium compounds and the like.
- Dimethyl formamide is appropriate for fibres of polyacrylonitrile.
- the continuous filaments to be decomposed are printed with the chemical compounds decomposing or destroying the fibre substances, advantageously in a thickened consistency, by means of rollers, patterns, screens and other devices showing a similar action, which are correspondingly discharged, provided with a relief pattern or engraving; then the filaments are dried and heated to such a temperature that a partial or complete decomposition of the fibre takes place.
- the process permits the production of fibres of uniform as well as of varying staple length in one and the same yarn. If printing is performed with printing dies arranged in parallel, a uniform length of staple is obtained, while printing dies of irregular arrangement result into a mixed staple as regards the length of the fibres.
- the spinning process does not suifer any interruption.
- the further treatment is carried out in known manner in the roving frame and the fine count spinning mill.
- a completely novel type of yarn can be manufactured by means of the process described above, by uniting to a yarn a number of endless filaments printed with the decomposing chemical substance in irregular intervals or in such a way that the printed spots are staggered, then twisting it, heating it to local decomposition and then stretching it. Thereby the filaments break at the weakened places without disconnecting the bundle of fibres.
- the endless filaments have now been transformed into a yarn whose properties correspond to those of a spun yarn, although it has been produced in a diiferent manner.
- Such a process is well suitable for coarse as well as for very fine yarns.
- the fibers After the fibers have been treated with the decomposing agents of the invention, they may be knitted or woven to form a textile before the fiber is decomposed.
- Example 1 A bundle of filaments of regenerated cellulose viscose is largely conducted over a flat support and provided by means of a gum roller or a metal roller with a thin print containing per 1000 grams of paste about 200 grams of aluminum sulphate and 700 grams of a wheat starchtragacanth thickening, for the local fixation of the aluminum sulphate.
- the printing is performed in the form of fine lines applied at intervals of 30-60-80-420 mm., for instance from the lower part left hand to the upper part right hand in an angle of 45.
- the material After printing, the material is heated for 35 minutes at about 110 C. and then torn, whereby the tear occurs at the places weakened by the printing paste. It is, however, also possible to heat for a prolonged time, for instance -20 minutes, at a temperature of 130140 C., then to steam for 1 hour.
- a length of staple given by the first print is obtained, i.e. the endless yarn has been transformed into staple fibre yarn.
- the final product is washed and further treated in the usual manner in order to produce tissues or knit goods.
- Example 3 grams grams grams grams grams Example 3 The process described in Example 2 is applied to a bundle of filaments consisting of a mixture, in a ratio of 1:1, of viscose rayon and acetate rayon. With the printing paste described in Example 2 the acetate rayon can be decomposed into staple fibres, but not the viscose rayon.
- Tissues and knit goods produced thereof are characterized by a fine, woolen handle, high smoothness and suppleness.
- Example 4 Endless filaments of polythylene terephthalate, of e.g. den., consisting of 24 single filaments, are printed before spooling or also at a later time, at intervals of, for instance, mm., with a paste containing per kilogram:
- the material is dried, woven and then subjected to a short action of heat, for instance of 30 seconds at 180- 210" C.
- a short action of heat for instance of 30 seconds at 180- 210" C.
- the endless filament is transformed into a staple yarn.
- a process for the manufacture of staple products which comprises locally applying a small stripe of a decomposing agent comprising guanadine carbonate and thiodiglycol as active ingredients to endless filaments of a polyethylene terephthalate fiber, and then severing said fiber by decomposition.
- a process for the manufacture of staple products which comprises locally treating endless filaments of polyethylene terephthalate at spaced intervals along their length with a decomposing agent comprising guanidine carbonate and thiodiglycols as active ingredients, and then severing said filaments by decomposition.
- a decomposing agent comprising guanidine carbonate and thiodiglycol as active ingredients applied to said filaments in the form of small stripes, and then severing said filaments by decomposition.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Artificial Filaments (AREA)
Description
June 27, 1961 NUSSLEIN 2,989,797
PROCESS FOR THE MANUFACTURE OF STAPLE YARNS BY FILAMENT DECOMPOSITION Filed NOV. 26, 1956 ENDLESS FILAMENTS 'OF POLYETHYLENE GLYCOL TEREPHTHALAT INV EN TOR.
Joseph Niisslein BY 2,989,797 Patented June 27, 1961 2,989,797 PROCESS FOR THE MANUFACTURE OF STAPLE YARNS BY FILAM'ENT DECOMPOSITION Joseph Niisslein, Frankfurt am Main, Germany, assiguor to Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius & Briining, Frankfurt am Main, Germany, a corporation of Germany Filed Nov. 26, 1956, Ser. No. 624,207 Claims priority, application Germany Nov. 30, 1955 Claims. (CI. 28-75) All fibres artificially produced are primarily obtained in continuous form. Filaments and fabrics consisting of such fibres show a very silky character, but not the full and warming handle of textile goods consisting of shortstapled fibrous material, as, for instance, wool or cotton. For this reason it is necessary to decompose the continuous filaments by means of cutting devices in order to obtain short fibres showing spinning properties and allowing of variations of length, for instance from 20 to 250 mm.
In the case of fibres of a high swelling capacity, for instance fibres of cellulose or protein regeneration prod ucts, the cutting can be performed very easily when the fibres are wet. In the case of completely synthetic fibres, however, eg those belonging to the polyamide, polyacryl and polyester series, the process of forming staples gives rise to a considerable consumption of energy and in increased abrasion of the knives.
In principle, the decomposition into short fibres shows the drawback that the single filaments arranged in parallel and leaving the spinning nozzles become snarled in the course of the cutting and finishing processes so that they have to be subjected to the same process in order to secure their parallel arrangement in the spinning process, as is necessary with natural fibres. Also the losses of fibres occurring during cutting and the following run over the carding machines represent a perceptible economical factor.
In order to avoid this consumption of substance and energy and to reduce the costs, numerous tests have been carried out in order to obtain, by tearing or cutting of endless slivers or cables of fibres arranged in parallel, staple fibres which keep their original parallel arrangement and can be spun for obtaining only the count of yarn desired.
These processes, however, caused multiple difiiculties. With fibres subjected to tearing, it is difficult precisely to keep the desired length of staple; in view of the fact that the fibres are overstretched by the tearing, undesired displacements of the original stretching values of the starting material occur.
The cutting process causes a rapid abrasion of the knives, thereby diminishing the capacity of the machines and, due to unsharp cutting or tearing, also injuriously affecting the quality of the staple.
Now, I have found that it is possible to obtain, in a completely novel manner, fibres showing spinning properties by applying onto bundles, cables or slivers of endless filaments, chemical compounds in the form of small stripes by means of patterns, rollers and the like, thereby damaging or destroying the fibres. This is to be done in such a way that the distance between one spot of application and the next one corresponds to the length of staple required. The material to be treated is to be subjected to such conditions that local breaks of the fibre substance sufficient for the decomposition of the continuous filament, take place.
The method of the invention is illustrated in the accompanying drawing, which shows a bundle of endless filaments having a decomposing agent applied to the filaments in the form of a stripe.
The present invention is to be distinguished from that described and claimed in copending application Serial No. 598,741, filed July 19, 1956, by Niisslein et al. The invention of the copending application relates to the selective printing of fabrics with decomposing agents, and not the use of such agents on fibers adaptable to subsequent fashioning into fabrics.
The chemical compounds to be chosen in each case depend upon the chemical nature of the fibrous substance. For instance, cellulose regeneration fibres can be destroyed by means of substances showing an acid reaction, whereas protein regeneration fibres can be destroyed by means of substances showing an alkaline reaction. Among the fibres which are synthetically produced, superpolyamide fibres are affected by strong mineral acids, acid amides, or aqueous chloral hydrate solution of 70% strength. In the case of polyester fibres excellent results can be attained with highly concentrated mineral acids as well as with several bases, especially with guanidine carbonate in connection with glycol, glycol derivatives, quarternary ammonium compounds and the like. Dimethyl formamide is appropriate for fibres of polyacrylonitrile.
The continuous filaments to be decomposed are printed with the chemical compounds decomposing or destroying the fibre substances, advantageously in a thickened consistency, by means of rollers, patterns, screens and other devices showing a similar action, which are correspondingly discharged, provided with a relief pattern or engraving; then the filaments are dried and heated to such a temperature that a partial or complete decomposition of the fibre takes place.
In the course of the subsequent stretching of the material the decomposition takes place by means of very low consumption of mechanical forces in order to obtain, with complete destruction, the staple desired. Partial decomposition is still of importance in the scope of the known tear spinning process. The decomposition of the fibres of high tensile strength takes place considerably more easily and more uniformly, since the spots of tear are already prepared.
The process permits the production of fibres of uniform as well as of varying staple length in one and the same yarn. If printing is performed with printing dies arranged in parallel, a uniform length of staple is obtained, while printing dies of irregular arrangement result into a mixed staple as regards the length of the fibres.
Since the parallel arrangement of the fibres can be completely preserved, the spinning process does not suifer any interruption. After decomposition of the continuous filaments into fibres the further treatment is carried out in known manner in the roving frame and the fine count spinning mill. By a corresponding classification applied in the process described above it ispossible directly to go over to the high stretching values, thereby considerably reducing consumption of time and labor. With appropriate arrangement of machinery it is, however, also possible immediately to start the twisting process, which is of special importance when fine yarns are concerned.
A completely novel type of yarn can be manufactured by means of the process described above, by uniting to a yarn a number of endless filaments printed with the decomposing chemical substance in irregular intervals or in such a way that the printed spots are staggered, then twisting it, heating it to local decomposition and then stretching it. Thereby the filaments break at the weakened places without disconnecting the bundle of fibres. The endless filaments have now been transformed into a yarn whose properties correspond to those of a spun yarn, although it has been produced in a diiferent manner.
Such a process is well suitable for coarse as well as for very fine yarns.
With kinds of fibres such as superpolyamides, polyacrylonitrile and its varities, polyvinyl alcohol, polyester fibres which undergo an intense stretch, appreciable effects can be produced by carrying out only a partial stretching, i.e. of two thirds of the usual extent, before printing the continuous filaments with the decomposing chemical substances, and using the last third for tearing the fibres after heating. It is also possible to use continuous filaments stretched to different extents whereby yarns which show other textile values are obtained.
After the fibers have been treated with the decomposing agents of the invention, they may be knitted or woven to form a textile before the fiber is decomposed.
Another possibility for the manufacture of novel yarns hitherto not existing consists in mixing the printed and dried bundle of filaments to be treated with yarns which have not been treated and finishing them in the manner described above or in treating together chemically difiering yarns so that a part of the yarn is attacked by the chemical substance chosen, while the other part is not alfected. In principle, the further treatment takes place in the same way as described above.
According to this method numerous novel kinds of yarns of great value for the textile industry, fashion and so on are obtained, particularly since mixing ratio, titre, count of yarn, twist, lustre, receptivity for dyes, curliness and the like may vary within wide limits.
The following examples serve to illustrate the invention; but they are not intended to limit it thereto:
Example 1 A bundle of filaments of regenerated cellulose viscose is largely conducted over a flat support and provided by means of a gum roller or a metal roller with a thin print containing per 1000 grams of paste about 200 grams of aluminum sulphate and 700 grams of a wheat starchtragacanth thickening, for the local fixation of the aluminum sulphate.
The printing is performed in the form of fine lines applied at intervals of 30-60-80-420 mm., for instance from the lower part left hand to the upper part right hand in an angle of 45.
By uniting single continuous filaments printed at irregular intervals, in order to form a yarn, and subsequent heating causing the destruction of the cellulose at the printed parts, a fibrous yarn is obtained which, in many respects. is equal to a spun yarn. After carbonization, i.e. heating of the fibre at the printed places, the acid residue is washed out.
of benzoyl peroxide,
of benzyl-acetate,
of British gum-tragacanth thickening, 50 grams of weakly sulphatized castor oil 200 grams of H 0.
After printing, the material is heated for 35 minutes at about 110 C. and then torn, whereby the tear occurs at the places weakened by the printing paste. It is, however, also possible to heat for a prolonged time, for instance -20 minutes, at a temperature of 130140 C., then to steam for 1 hour. A length of staple given by the first print is obtained, i.e. the endless yarn has been transformed into staple fibre yarn. The final product is washed and further treated in the usual manner in order to produce tissues or knit goods.
grams grams grams Example 3 The process described in Example 2 is applied to a bundle of filaments consisting of a mixture, in a ratio of 1:1, of viscose rayon and acetate rayon. With the printing paste described in Example 2 the acetate rayon can be decomposed into staple fibres, but not the viscose rayon.
In this way a mixed yarn of continuous filaments enclosing a bundle of staple fibres is obtained. Tissues and knit goods produced thereof are characterized by a fine, woolen handle, high smoothness and suppleness.
Example 4 Endless filaments of polythylene terephthalate, of e.g. den., consisting of 24 single filaments, are printed before spooling or also at a later time, at intervals of, for instance, mm., with a paste containing per kilogram:
of crystal gum (1:2) of British gum (1:1) of thiodiglycol,
of guanidine carbonate, of H 0.
The material is dried, woven and then subjected to a short action of heat, for instance of 30 seconds at 180- 210" C. In view of the decomposition immediately taking place at the printed places, the endless filament is transformed into a staple yarn.
I claim:
1. A process for the manufacture of staple products which comprises locally applying a small stripe of a decomposing agent comprising guanadine carbonate and thiodiglycol as active ingredients to endless filaments of a polyethylene terephthalate fiber, and then severing said fiber by decomposition.
2. A process as in claim 1 in which said fiber is decomposed by heating.
3. A process as in claim 1 in which said fiber is severed by decomposition after the fiber has been woven to form a textile.
4. A process as in claim 3 in which said fiber is decomposed by heating.
5. A process as in claim 1 in which said fiber is severed by decomposition after the fiber has been knitted to form, a textile.
6. A process as in claim 5 in which said fiber is decomposed by heating.
7. A process for the manufacture of staple products which comprises locally treating endless filaments of polyethylene terephthalate at spaced intervals along their length with a decomposing agent comprising guanidine carbonate and thiodiglycols as active ingredients, and then severing said filaments by decomposition.
8. A process as in claim 7 in which said fiber is decomposed by heating.
9. Yarns obtained by locally treating endless filaments of polyethylene terephthalate with a decomposing agent comprising guanidine carbonate and thiodiglycol as active ingredients applied to said filaments in the form of small stripes, and then severing said filaments by decomposition.
300 grams 300 grams grams 50 grams 250 grams References Cited in the file of this patent UNITED STATES PATENTS 2,003,400 Taylor et al. June 4, 1935 2,044,130 Sowter June 16, 1936 2,362,768 Morgan Nov. 14, 1944 2,590,402 Hall et al. Mar. 25, 1952 2,597,708 Cresswell May 20, 1952 2,616,822 Danielson Nov. 4, 1952 2,647,104 Shivers July 28, 1953 2,721,440 New Oct. 25, 1955 2,784,458 Preston Mar. 12, 1957
Claims (1)
1. A PROCESS FOR THE MANUFACTURE OF STAPLE PRODUCTS WHICH COMPRISES LOCALLY APPLYING A SMALL STRIPE OF A DECOMPOSING AGENT COMPRISING GUANADINE CARBONATE AND THIODIGLYCOL AS ACTIVE INGREDIENTS TO ENDLESS FILAMENTS OF A POLYETHYLENE TEREPHTHALATE FIBER, AND THEN SEVERING SAID FIBER BY DECOMPOSITION.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2989797X | 1955-11-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2989797A true US2989797A (en) | 1961-06-27 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US624207A Expired - Lifetime US2989797A (en) | 1955-11-30 | 1956-11-26 | Process for the manufacture of staple yarns by filament decomposition |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2989797A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3276945A (en) * | 1957-08-23 | 1966-10-04 | Owens Corning Fiberglass Corp | Strand product |
| US4086055A (en) * | 1976-10-04 | 1978-04-25 | Milliken Research Corporation | Surface modified continuous filament yarn and method of producing same |
| US4113432A (en) * | 1977-05-23 | 1978-09-12 | Milliken Research Corporation | Method for modifying fibers of a fabric and the products so produced |
| US5577307A (en) * | 1993-06-30 | 1996-11-26 | Itoi; Toru | Method for producing multi-ply fabric with water soluble thread |
| US20020133924A1 (en) * | 2001-03-26 | 2002-09-26 | Yacov Cohen | Novel process for the manufacture of super fine woven wool fabric with single yarn in the warp having improved weavability |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2003400A (en) * | 1932-07-04 | 1935-06-04 | Celanese Corp | Manufacture of staple fiber yarns |
| US2044130A (en) * | 1933-02-15 | 1936-06-16 | Celancse Corp | Textile yarn and the manufacture thereof |
| US2362768A (en) * | 1940-08-03 | 1944-11-14 | Arnold Hoffman & Co Inc | Moth repelling product |
| US2590402A (en) * | 1948-08-13 | 1952-03-25 | Ici Ltd | Lightweight polymethylene terephthalate fabric produced by alkali treatment |
| US2597708A (en) * | 1948-12-30 | 1952-05-20 | American Cyanamid Co | Antistatic agent, treatment of shaped articles therewith, and treated articles |
| US2616822A (en) * | 1949-09-14 | 1952-11-04 | Us Rubber Co | Protection of cellulose fiber against heat aging |
| US2647104A (en) * | 1951-07-30 | 1953-07-28 | Du Pont | Linear polyester composition |
| US2721440A (en) * | 1951-02-13 | 1955-10-25 | American Viscose Corp | Process for producing direct spun yarns from strands of continuous fibers |
| US2784458A (en) * | 1949-07-08 | 1957-03-12 | Deering Milliken Res Corp | Process and apparatus for converting continuous filamentary material into filaments of staple length |
-
1956
- 1956-11-26 US US624207A patent/US2989797A/en not_active Expired - Lifetime
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2003400A (en) * | 1932-07-04 | 1935-06-04 | Celanese Corp | Manufacture of staple fiber yarns |
| US2044130A (en) * | 1933-02-15 | 1936-06-16 | Celancse Corp | Textile yarn and the manufacture thereof |
| US2362768A (en) * | 1940-08-03 | 1944-11-14 | Arnold Hoffman & Co Inc | Moth repelling product |
| US2590402A (en) * | 1948-08-13 | 1952-03-25 | Ici Ltd | Lightweight polymethylene terephthalate fabric produced by alkali treatment |
| US2597708A (en) * | 1948-12-30 | 1952-05-20 | American Cyanamid Co | Antistatic agent, treatment of shaped articles therewith, and treated articles |
| US2784458A (en) * | 1949-07-08 | 1957-03-12 | Deering Milliken Res Corp | Process and apparatus for converting continuous filamentary material into filaments of staple length |
| US2616822A (en) * | 1949-09-14 | 1952-11-04 | Us Rubber Co | Protection of cellulose fiber against heat aging |
| US2721440A (en) * | 1951-02-13 | 1955-10-25 | American Viscose Corp | Process for producing direct spun yarns from strands of continuous fibers |
| US2647104A (en) * | 1951-07-30 | 1953-07-28 | Du Pont | Linear polyester composition |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3276945A (en) * | 1957-08-23 | 1966-10-04 | Owens Corning Fiberglass Corp | Strand product |
| US4086055A (en) * | 1976-10-04 | 1978-04-25 | Milliken Research Corporation | Surface modified continuous filament yarn and method of producing same |
| US4113432A (en) * | 1977-05-23 | 1978-09-12 | Milliken Research Corporation | Method for modifying fibers of a fabric and the products so produced |
| US5577307A (en) * | 1993-06-30 | 1996-11-26 | Itoi; Toru | Method for producing multi-ply fabric with water soluble thread |
| US20020133924A1 (en) * | 2001-03-26 | 2002-09-26 | Yacov Cohen | Novel process for the manufacture of super fine woven wool fabric with single yarn in the warp having improved weavability |
| US6823569B2 (en) * | 2001-03-26 | 2004-11-30 | Polgat Textiles Co. | Process for the manufacture of super fine woven wool fabric with single yarn in the warp having improved weavability |
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