US3057038A - Wet spun cellulose triacetate - Google Patents
Wet spun cellulose triacetate Download PDFInfo
- Publication number
- US3057038A US3057038A US729980A US72998058A US3057038A US 3057038 A US3057038 A US 3057038A US 729980 A US729980 A US 729980A US 72998058 A US72998058 A US 72998058A US 3057038 A US3057038 A US 3057038A
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- United States
- Prior art keywords
- filaments
- jet
- cellulose triacetate
- bundle
- liquid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920002284 Cellulose triacetate Polymers 0.000 title claims description 35
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 title claims description 35
- 239000000463 material Substances 0.000 claims description 37
- 239000007788 liquid Substances 0.000 description 37
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 36
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 238000002788 crimping Methods 0.000 description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 238000001035 drying Methods 0.000 description 9
- 239000000314 lubricant Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 230000007423 decrease Effects 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- 230000008961 swelling Effects 0.000 description 6
- 230000009471 action Effects 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 238000002166 wet spinning Methods 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- ATSGLBOJGVTHHC-UHFFFAOYSA-N bis(ethane-1,2-diamine)copper(2+) Chemical compound [Cu+2].NCCN.NCCN ATSGLBOJGVTHHC-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- WGLUMOCWFMKWIL-UHFFFAOYSA-N dichloromethane;methanol Chemical compound OC.ClCCl WGLUMOCWFMKWIL-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- ZVZFHCZCIBYFMZ-UHFFFAOYSA-N 6-methylheptoxybenzene Chemical compound CC(C)CCCCCOC1=CC=CC=C1 ZVZFHCZCIBYFMZ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 244000148064 Enicostema verticillatum Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 244000278243 Limnocharis flava Species 0.000 description 1
- 235000003403 Limnocharis flava Nutrition 0.000 description 1
- 206010027626 Milia Diseases 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- 239000012932 acetate dye Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- -1 methanol Chemical compound 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G1/00—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
- D02G1/16—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics using jets or streams of turbulent gases, e.g. air, steam
- D02G1/165—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics using jets or streams of turbulent gases, e.g. air, steam characterised by the use of certain filaments or yarns
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65H—HANDLING THIN OR FILAMENTARY MATERIAL, e.g. SHEETS, WEBS, CABLES
- B65H54/00—Winding, coiling, or depositing filamentary material
- B65H54/76—Depositing materials in cans or receptacles
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/06—Wet spinning methods
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/22—Formation of filaments, threads, or the like with a crimped or curled structure; with a special structure to simulate wool
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
- D01F2/28—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65H—HANDLING THIN OR FILAMENTARY MATERIAL, e.g. SHEETS, WEBS, CABLES
- B65H2701/00—Handled material; Storage means
- B65H2701/30—Handled filamentary material
- B65H2701/31—Textiles threads or artificial strands of filaments
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2922—Nonlinear [e.g., crimped, coiled, etc.]
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2965—Cellulosic
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2973—Particular cross section
- Y10T428/2978—Surface characteristic
Definitions
- This invention relates to the production of lilamentary materials.
- Another object of this invention is the provision of a new and crimped artificial filamentary material.
- a solution of a filament-forming material in a liquid organic solvent is extruded through a multi-oriced spinnerette into a liquid coagulant to form a running bundle of paral lel filaments swollen with liquid.
- the bundle is drawn through and out of the coagulating liquid, whereupon the filaments cling tightly together under the action of tension in the bundle and the action of surface tension of entrained liquid.
- the individual filaments of the bundles are then separated from each other and the liquid which swelled the filaments is removed therefrom while the filaments are maintained in substantially separated and tensionless condition.
- the coagulant is a mixture of a solvent and a non-solvent for the filament-forming material.
- the present invention has shown its greatest utility in the wet-spinning of cellulose triacetate from solutions thereof in methylene chloride or mixtures of methylene chloride and small amounts of an alcohol such as methanol, using a cellulose triacetate having an acetyl value of at least 60%, preferably above 61%, calculated as acetic acid.
- cellulose triacetate spinning solution may be extruded into a bath of coagulant, or spin-bath, comprising methylene chloride mixed with methanol or other lower aliphatic alcohol in accordance with the teachings of the copending application of Jesse L. Riley, entitled Spinning, Serial No.
- the resulting filaments are stretched in the spin-bath, which has a considerable swelling power for the cellulose triacetate, the stretching being effected by taking up the swollen filaments at a higher linear speed than the linear speed at which they are extruded.
- the stretching force is most conveniently applied by means of a positively driven feed roll, such as a godet roll, over which the laments pass, as a bundle, after they leave the spin bath.
- the bundle of swollen filaments leaving the feed roll generally carries a considerable proportion of liquid, for example 200% or more of liquid based on the weight of the cellulose triacetate.
- a This bundle may comprise several thousand individual filaments.
- the running bundle of parallel swollen cellulose triacetate filaments leaving the feed roll is passed through a zone where the filaments are separated from each other.
- a suitable gas jet may be used for this purpose, the construction of the jet, and the pressure of and temperature of the gas delivered thereto, being such that the filaments leaving the jet are not looped or tangled but are parallel and separate. It is preferable to remove a substantial portion of the liquid from the bundle of filaments before it reaches the jet. This may be done by the use of suitable arrangements of liquid-stripping guides, sucking devices engaging the bundle before or after it passes over the feed roll, and heated evaporative zones through which the bundle passes on its way to the jet.
- the amount of preliminary liquid removal be such that the lfilaments of the bundle entering the jet are wet with liquid, that is, they carry free liquid on their surfaces.
- the proportion of liquid in the filaments entering the jet is preferably within the range of about 1GO to 250%, based on the weight of filament-forming material.
- the gas fed to the jet should be heated to increase the evaporation of swelling liquid which occurs as the bundle passes through and beyond the jet.
- the filaments will be under tension at some point in the jet, due to the force of the gas stream, and since crimping takes place when the swelling liquid is removed from the filaments while they are in substantially separated, tensionless condition, too great a degree of evaporation in the jet may interfere with the crimping tendency.
- the further evaporation of the swelling liquid, and the resulting crimping of the separated untensioned continuous filaments may be effected continuously by conveying the parallel separated filaments in a stream of Patented Oct. 9, 1962 ⁇ heated air or other gas and in substantially tensionless condition, until sufiicient swelling liquid is removed.
- the crimping occurs while the separated filaments are fioating in the gas stream.
- This crimping is not dependent on any turbulent flow of the carrying stream, and, in fact, gross turbulence, which would tend to entangle filaments or cause snarls or loopiness, is undesirable and is preferably avoided by suitable shielding to avoid drafts or other outside influences during drying.
- the stream carrying the filaments may pass through a tunnel or a long chute so constructed as to minimize turbulence.
- the filaments After the filaments have dried sufficiently to set the crimp firmly therein, they are brought together on a suitable collection device.
- they may pass through the nip of a pair of driven takeup rolls for delivery to a packaging device, such as the tow-packaging device shown in the copending application of Weber et al. Serial No. 262,856, filed December 21, 1951, now Patent No. 2,798,348.
- the take-up rolls should be driven at such a speed that the rate of movement of the filaments at said rolls is less than the peripheral speed of the feed roll.
- the separated filaments leaving the air jet are allowed to fall freely onto a slowly moving porous belt or other conveying means which is passed through a drying zone.
- the filaments should be deposited on the belt, which may be in the form of an endless screen, in such a manner that there is a minimum of contact or crossing-over of filaments and therefore a minimum of interaction between adjacent filaments during the period when the filaments are crimping spontaneously, though some contact is permissible and generally unavoidable. It is convenient to lay the voluminous bundle of filaments onto belt back-and-forth across the belt, in a sinuous configuration.
- the filaments tend to develop slightly less crimp than in the intermediate portions of the belt Where the bundle of filaments is generally straight and where the bundle is looser.
- This effect may be reduced by directing the hot air, used for drying the filaments, upwardly in a gentle stream through the pores of the belt; this makes for a more effective relaxation and separation of the filaments on the belt.
- the force of the stream of hot air is not great enough to actually lift the bundle of filaments from the belt.
- the extent of separation of the filaments need not be great so long as they are kept substantially independent of each other.
- the diameter of the bundle leaving the air jet was 3A; inch; in this case, by calculation, the average distance between adjacent filaments was on the order of 700-800 microns.
- the extent of removal of liquid from the separated, untensioned filaments should be such that the filaments are brought to a substantially unswollen condition.
- spin bath -it is preferable to continue the drying, while the filaments are separated and untensioned, until the liquid content is reduced to about or less, based on the weight of the cellulose triacetate.
- the crimping obtained in accordance with this invention is not dependent on the use of high temperatures during removal of the liquid.
- it is desirable to feed air at a temperature in the range of about 70 to 140 C. to the jet but good results have been obtained using air at room temperature for this purpose.
- Even when hot air at 1407 C. is fed to the jet the temperature of the air leaving the jet with the filaments is probably in the neighborhood of 50 C., due to cooling resulting from evaporation of methanol and methylene chloride.
- air at a temperature of about to 90 C. has been supplied to the drying zone where the crimping of the filaments occurs, but here again the actual temperature of the filaments during the time crimping takes place is probably less than 65 C.
- yIt is advantageous to apply a textile lubricant to the filaments.
- This lubricant is best applied after the removal of liquid from the filaments, that is, when the filaments are in non-swollen condition.
- the lubricant which may, for example, be that described in United States Patent No. 2,805,992, 4issued to Fortess et al. on September 10, 1957, is conveniently supplied -by passing the unswollen filaments over a roller, carrying a film of lubricant, before the filaments are engaged in the nip of the take-up rolls. More desirably, a mist of the lubricant may be applied by a suitable spraying device at this Ipoint.
- lubricant in the form of a -rnist or spray results in a more uniform distribution of lubricant throughout the bundle and avoids the development of tension which would result from passage of the bundle over a lubricating roller or other surface under such conditions as to secure uniformity of application.
- the process of this invention is especially vaiuable for the production of a crimped tow, made up of a thousand or more continuous filaments and having a total denier of 3000 or more, the denier per filament being about 1 to 6.
- crimp tow mechanically, as by passing the tow through a suitable heated stufiing box type of crimper.
- Such mechanical crimping damages the individual filaments of the tow, particularly when a highly crimped material, having five or more crimps per inch, is produced.
- the crimps in all the filaments of the tow are aligned and more or less in the same plane.
- the filaments of the tow are not damaged at all.
- the crimps in adjacent filaments are randomly arranged, out of alignment; the crimp being three-dimensional, either helically or randomly threedimensional, and not substantially in a single plane.
- the tow is much more voluminous or lofty than the conventional tows.
- Typical crimped filaments produced in accordance 'with this invention contain 8 or more e.g. 8 to l2, fine crimps per inch, the amplitude of the crimp being irregular but generally being on the order of 1 mm. and the percent crimp, based on the straightened length, being above about 4%.
- Percent crimp is defined as Straightened length-crimped length
- Straightened length ferred to above the use of certain critical proportions of methylene chloride in the spin bath results in the production of filamentary materials of outstanding physical properties (e.g. tenacity of at least 1.8 grams per denier and elongation of at least 18%).
- proportions of methylene chloride within the scope of the Riley application.
- the proportions of methylene chloride in the spin bath are within the range defined by the formula where C is the concentration in percent and T is the temperature in C.
- crimped cellulose triacetate filamentary materials whose mechanical properties are superior to those of any crimped filaments obtained by the wet, dryor melt-spinning of cellulose triacetate.
- crimped filamentary materials whose tenacity is at least 1.8, usually above 2, grams per denier and whose elongation is at least 18%, usually above 20%, even for filaments whose denier is in the range of 1.5 to 4.
- the energy of rupture i.e. the area under the stress-strain curve from zero stretch to break, is high.
- These crimped filamentary materials are characterized by radial uniformity.
- a filamentary material which is non-uniform exhibits different properties as compared with the original material, while a radially uniform material has the same properties as before.
- the surface removal can be effected, for example, by wetting the filaments to be tested in cold water containing 0.1 gram per liter of Triton X-l (iso-octyl phenyl ether of polyethylene glycol) then immersing them in 1000 times their weight of a 50 grams per liter solution of sodium hydroxide at 95 C. for from 30 seconds to 3 minutes, and quickly transferring them to cold running water for minutes.
- the filaments are then soured in acetic acid for minutes and again rinsed in running water for l5 minutes.
- the filaments After drying in air, the filaments are immersed at room temperature for 3 minutes in a solution made up of equal weights of cupriethylene diamine and lwater to dissolve the cellulose skin formed by the saponication. The filaments are then rinsed, soured, rinsed and dried as before.
- 2.5 denier filaments produced in accordance with the invention pick up 0.24% by weight of dyestuff after being immersed 5 minutes in the dyebath previously set forth Iand 0.34% after 15 minutes. Removal of a surface layer 47x10'6 cm. thick does not increase the dyeing rate. Actually there is a slight decrease to 0.23% and 0.31% in 5 and l5 minutes, respectively, i.e. approximately the same rate as de-surfaced dry spun cellulose triacetate filaments.
- the dyebath was water containing 50 grams per liter of dispersed Amacel Red 2B (a red cellulose acetate dye), 1 gram per liter of Igepon T-Sl (a dispersing agent) and l gram per liter of sodium hexametaphosp'hate; the bath was maintained at C.
- Amacel Red 2B a red cellulose acetate dye
- Igepon T-Sl a dispersing agent
- the filamentary materials of this invention show a relatively high overall birefringence after complete saponification (according to the technique described below) of said materials.
- the overall birefringence of the saponified material is above about 0.031, typical values being in the range of about 0.034 to 0.037.
- This overall birefringence is the sum of the birefringences through the fiber and is measured, in conventional manner, by a transmission technique.
- the filamentary material is saponified completely by immersion for at least 3() minutes in times its weight of a solution containing, by weight, 5 parts of sodium hydroxide, 12 parts of sodium acetate, 10 parts of dimethylsulfoxide land 73 parts of lwater, at 80 C.
- Completion of saponication can be checked by wetting the filamentary material with l-N cupriethylene diamine solution; if, as viewed under a microscope, the filamentary material dissolves completely in 30 seconds, saponification is complete; if not complete, the time of immersion in the s-aponifying liquor can be increased.
- the filamentary material is rinsed with distilled water until the rinse water is neutral.
- the saponified material is air dried.
- the treatment does not cause shrinkage or loss of strength.
- the overall birefningence, as opposed to merely surface birefringence, is determined in customary manner, as with a Berek compensator using polarized light.
- Cellulose triacetate filamentary materials produced in accordance Iwith this invention exhibit definite rubbery properties at elevated temperatures. This is demonstrated in the following manner: A denier 40 filament yarn is held at constant length r(eg. 10 inches) and heated to a temperature of 220 C. ⁇ at a just perceptible initial tension (about 0.03 g.). The temperature is then cycled between 217 C. and 223 C. It will be found that the tension on the filament increases as the temperature increases and decreases very perceptibly as the temperature decreases, typical of a rubber. By Way of comparison, if the temperature of the filament is cycled between 162 C. and 168 C., the tension will be found to decrease as the temperature increases, typical of a glass.
- the cellulose triacetate filamentary material obtained in accordance with this invention may be heat treated to raise the safe ironing -tempenature of fabrics produced therefrom and to improve the dimensional stability, resistance to creasing, permanence of pleating, and the like.
- the filamentary matenial of this invention shows substantially no shrinkage or decrease of tenacity on such heat treatment. In fact, the tenacity may even increase.
- a filament produced in accordance with this invention and having an original tenacity of 2.15 grams per denier, when heat treated in lair at 210 C. for minutes shrinks fless than 1% and has a final tenacity of 2.37 g./den.
- Cellulose triacetate filamentary material produced in accordance with the invention is also charatcerized by resistance to creep yat elevated temperature. This is demonstrated as follows: One end of la filament is anchored within a lhorizontal heating tube. inches from the anchored end, the filament is knotted to a glass lament which extends outside the tube and runs over a pulley. A weight is suspended from the protruding end of the glass filament. glass filament the tube is heated ⁇ and the displacement of the weight with change in temperature is noted. Cellulose triacetate filaments produced by idry spinning the initial solutions begin to creep at about 168 C. The instant filamentary materials do not creep comparably below ⁇ about 178-183 C. The rate ⁇ and amount of creep for dryspun filaments under a lo-ad of 0.033 gram per denier are only reached for the instant ilamentary materials at a load equal to or in excess of 0.067 gram per denier.
- FIG. 1 illustnates, diagrammatically, the process of this invention.
- FIGS. 2 and 3 are two views of a modiiication of the drying and crimping stage of the process
- FIG. 4 is a cross-sectional view of an air jet, drawn to scale, as indicated,
- FIG. 5 is an enlarged photograph of la crimped tow produced in accordance with this invention, yand 'also showing an individual crimped lament, alongside said tow.
- FIG. 6 is a photograph showing the cross-section of a crimped tow produced according to this invention, showing the circular cross-sections of the individual filaments.
- FIG. 7 is a photomicrograph of the single filament of FIG. 5, the filament being tensioned suiiiciently to pull out the crimp temporarily land being shadowed with chromium to show the pebbled surface configuration.
- Like reference numerals designate like parts in the several views of the drawing.
- reference numeral 11 designates a spinnerette mounted in suitable vessel 12 filled with spin bath liquid which is supplied to said vessel by a pump 13.
- the ⁇ spin bath liquid enters the vessel through a sparger 14, passing through a layer of metallic wool 16 to reduce turbulence.
- the spin bath also lills a vertical spin column 17 which communicates with the vessel 12 and whose tapered lower end 18 is positioned directly above and surrounds the spinnerette 11.
- a spinning solution, or dope is forced by the action of a pump 19 through the apertures of the spinnerette 11 and into the spin bath to form filaments 21, which are drawn upward through the spin column 17, and over a pulley 22, by the action of a driven feed roll 23.
- the spin bath which moves slowly up the spin column 17, fiows over a weir 24 to a catch basin 26, from which it is withdrawn and, after purification, recirculated to the vessel 12 through the pump 13.
- Some of the spin bath liquid adheres to the filaments leaving the column 17; part of this adherent liquid is removed mechanically by suitable devices such as stripper guides 27 and vacuum strippers 28 engaged With various size weights suspended from the by the filamentsv as they pass to the feed roll 23.
- the still wet filaments in the form of a bundle or tow make several wraps around the feed roll 23 and the usual idler roll 29 associated therewith and then are fed to a predrier 31, supplied with hot air.
- the tow passes through a horizontal air jet 32, where it is subjected to a stream of heated air and from which it emerges as a horizontal stream 33 of parallel separated filaments, supported in substantially tensionless condition in a stream of heated air passing through an enclosed drying zone .34.
- a long smooth horizontal chute 36 mounted just below the stream of air and out of contact with the filaments helps toI control the direction of air flow and to support the filaments in the air stream.
- the filament-s, now thoroughly dry and crimped, are passed under a sprayer 37, where a mist of textile lubricant is applied, and are then taken up as a continuous bundle by means of a pair of driven rolls 33 and 39. This bundle, or tow 41, is collected in any suitable manner, as in a container 42.
- the separated filaments 33 emerging from the jet 32 fall, under their own weight, through a pivoted traverse tube 46, to an endless moving screen 47, driven through rollers 48, which screen carries them through a drying oven 49.
- the ltraverse tube 46 is rocked on its pivot 51, by suitable mechanism 52, to distribute the filaments back and forth across :the width of the moving screen 47, and the rate of movement of the traverse tube and screen are so coordinated the loose bundle of filaments 53 is laid back and forth across the belt, successive traverses of the bundle being ⁇ side by side and not one on top of another.
- the jet 32 comprises a main body 56 having an axial venturi passage 57 and three circular side inlets 58, spaced evenly around the axis, for the introduction of compressed air into the entrance end 59 of said passage.
- Fitted axially within said entrance end 59 is a tapered yarn inlet tube 61, which terminates just before the throat 62 of said venturi passage 57.
- the yarn passes axially through the tube 61 while the air travels around said tube, the yarn and air moving together from the throat 61 to the wider discharge end of the venturi passage, and then out into the atmosphere.
- the jet 32 is symmetrical about its axis, all cross-sections at right angles to the axis being circular, except, of course, for the side inlets 58.
- FIG. 4 is drawn precisely to the scale shown thereon.
- Example I A solution containing 21.5% of cellulose tn'acetate of 61.5% acetyl value, calculated as acetic acid, and of intrinsic viscosity 2.0 (measured on cellulose regenerated, without degradation, from said cellulose triacetate) dissolved in a mixture of parts of methylene chloride and 10 parts of methanol, is extruded upward from a spinnerette having 1396 circular holes each 0.10 mm. in diameter into a spin bath containing 43.0% methylene chloride and 57.0% methanol at a temperature of 32 C. By the action of a feed roll mounted outside the spin bath the resulting filaments are drawn upward through a spin tube having a height of cm.
- the filaments emerging from the top of the spin column carry about 30G-400% of liquid, based on the weight of cellulose triacetate.
- the composition of this liquid is substantially the same as that of the spin-bath.
- the wet filaments are brought together to form a tow and are passed successively over stripper guides, a pulley and a sucking roll, which remove some of the liquid, so that their liquid content is about 250% at the feed roll.
- the feed roll moves the wet tow at the rate of 50y meters per minute under a tension of 186 grams (measured at the 9 top of the column after the tow passes the stripper guides), the draw-down ratio being 6.6:1.
- the total denier (on a dry basis) of this 1396 filament tow is 4188.
- the tow passes through a predryer in the form of an air jet through which the tow passes axially and which is supplied with air at a temperature of 120 C. and a pressure of 50 p.s.i.g. at the rate of 7.6 s.c.f.m. (i.e. measured at 14.7 p.s.i.g. and 62 F.).
- the still wet swollen iilaments emerging from the predryer pass directly to an air aspirator, constructed as shown in FIG.
- the resulting tow is much more voluminous than mechanically crimped tow.
- the individual iilaments have 3-dimensional, irregular and sinusoidal crimps and have an amplitude of about 1 mm. and a frequency of about 10 crimps per inch.
- the percent crimp, based on the straightened length, is about 5.1%.
- the crimp is retained even when the filaments are strained past their yield point, with appreciable crimp being retained even after a strain of 5% is applied.
- the crimp is retained after washing in hot water (e.g. 70 C.).
- the individual laments which are substantially circular in cross-section, have a tenacity at break of 1.8 grams per denier and an elongation at break (based on their uncrimped length) of 22%.
- Example II A solution containing 21.5% of cellulose triacetate of acetyl value 61.5%, based on acetic acid, dissolved in a mixture of 90 parts methylene chloride and 10 parts oft methanol, is forced through a spinnerette, having 40 circular holes each 0.1 mm. in diameter, into a spin bath containing 40% of methylene chloride and 60% methanol at a temperature of 33 C. and is taken up on a feed roll at the rate of 50 meters per minute, at a draw-down ratio of 6.611.
- the resulting wet 40iilament yarn, having a total denier (on a dry basis) of 120 is passed through an air aspirator supplied with air at p.s.i.g.
- a crimped tilamentary material of cellulose triacetate having a tenacity of at least 1.8 grams per denier, an elongation o-f at least 18% and a pebbled surface.
- a crimped cellulose triacetate filament exhibiting a tenacity of at least 1.8 grams per denier, an elongation of at least 18%, a pebbled surface, radial uniformity, an overall birefringence above about 0.031 when completely sapOnied, rubbery properties at 220 C., resistance to creep at 168 C., and substantially no shrinkage on heat treatment.
- a crimped lilamentary material of cellulose triacetate having a tenacity of about 1.8 grams per denier, an elongation of about 22% and a pebbled surface.
- a crimped filamentary material of cellulose triacetate having a tenacity of about 1.8 to 2.15 grams per denier and an elongation of about 18% to about 22% and a pebbled surface.
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Description
Oct. 9, 1962 J. W. SOEHNGEN WET SPUN CELLULOSE TRIACETATE Filed April 21, 1958 3 Sheets-Sheet 1 Oct. 9, 1962 .1. w. SOEHNGEN WET sPuN cELLULosE TRIACETATE 3 Sheets-Sheet 2 Filed April 21, 1958 .NGI
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Amp/vers Oct. 9, 1962 J. w. soEHNGEN WET sPUN CELLULOSE TRIACETATE 3 Sheets-Sheet 3 Filed April 2l, 1958 FIG. 5.
IN VEN TOR. dof//v M Sow/Gay @MMM/11M Unite Sttes This application is a continuation-impart of copending application Serial No. 663,815 filed lune 5, 1957.
This invention relates to the production of lilamentary materials.
It is an object of this invention to provide a new and improved method for making crimped continuous artificial filaments.
Another object of this invention is the provision of a new and crimped artificial filamentary material.
Other objects of this invention will be apparent from the following detailed description and claims. In this description and claims all proportions are by weight, unless otherwise indicated.
In accordance with one aspect of this invention a solution of a filament-forming material in a liquid organic solvent is extruded through a multi-oriced spinnerette into a liquid coagulant to form a running bundle of paral lel filaments swollen with liquid. The bundle is drawn through and out of the coagulating liquid, whereupon the filaments cling tightly together under the action of tension in the bundle and the action of surface tension of entrained liquid. The individual filaments of the bundles are then separated from each other and the liquid which swelled the filaments is removed therefrom while the filaments are maintained in substantially separated and tensionless condition. -In accomplishing this, it is most convenient to pass the bundle of swollen parallel continuous filaments through an appropriate jet of air or other evaporative gas in such a manner that the continuous filaments are separated but remain substantially parallel, and then to remove the liquid from the separated parallel filaments by evaporation while these filaments are under substantially no tension. During the removal of the liquid, without tension, spontaneous crimping of the filaments occurs.
Preferably, the coagulant is a mixture of a solvent and a non-solvent for the filament-forming material.
The present invention has shown its greatest utility in the wet-spinning of cellulose triacetate from solutions thereof in methylene chloride or mixtures of methylene chloride and small amounts of an alcohol such as methanol, using a cellulose triacetate having an acetyl value of at least 60%, preferably above 61%, calculated as acetic acid. I he cellulose triacetate spinning solution may be extruded into a bath of coagulant, or spin-bath, comprising methylene chloride mixed with methanol or other lower aliphatic alcohol in accordance with the teachings of the copending application of Jesse L. Riley, entitled Spinning, Serial No. 638,4l4, filed AFebruary 5, 1957; the entire disclosure of said application of Riley is hereby incorporated, by reference, into the present application. As disclosed in said Riley application, the resulting filaments are stretched in the spin-bath, which has a considerable swelling power for the cellulose triacetate, the stretching being effected by taking up the swollen filaments at a higher linear speed than the linear speed at which they are extruded. The stretching force is most conveniently applied by means of a positively driven feed roll, such as a godet roll, over which the laments pass, as a bundle, after they leave the spin bath. The bundle of swollen filaments leaving the feed roll generally carries a considerable proportion of liquid, for example 200% or more of liquid based on the weight of the cellulose triacetate.
A This bundle may comprise several thousand individual filaments.
In accordance with this invention, the running bundle of parallel swollen cellulose triacetate filaments leaving the feed roll is passed through a zone where the filaments are separated from each other. As previously stated, a suitable gas jet may be used for this purpose, the construction of the jet, and the pressure of and temperature of the gas delivered thereto, being such that the filaments leaving the jet are not looped or tangled but are parallel and separate. It is preferable to remove a substantial portion of the liquid from the bundle of filaments before it reaches the jet. This may be done by the use of suitable arrangements of liquid-stripping guides, sucking devices engaging the bundle before or after it passes over the feed roll, and heated evaporative zones through which the bundle passes on its way to the jet. It is important, however, not to remove too much of the liquid before the bundle enters the jet, since unless the separated filaments emerging from the jet are still in swollen condition they will not crimp. Furthermore, the swollen filaments in the bundle leaving the feed roll are in an adhesive condition so that if too much of the solvent is evaporated before the bundle reaches the jet the swollen parallel filaments will tend to stick to each other and will not be separated in the jet. It is therefore preferable that the amount of preliminary liquid removal be such that the lfilaments of the bundle entering the jet are wet with liquid, that is, they carry free liquid on their surfaces. On the other hand, when the bundle entering the gas jet carries too much liquid, it is found that it is very diliicult to separate the filaments in the jet, presumably because of the effect of the surface tension of the liquid; if in this case the flow of gas through the jet is increased in an attempt to increase the separating force on the filaments, the force of the gas blast generally tends to tangle the filaments. The proportion of liquid in the filaments entering the jet is preferably within the range of about 1GO to 250%, based on the weight of filament-forming material.
Regarding the gas jet, very good results have been obtained by the use of a commercial venturi type wateraspirator jet; i.e. a device which is usually employed forcreating a vacuum by sucking air or other gas into a stream of water passing through a venturi. In the practice of the present invention, this jet is, of course, used in an entirely different manner. Thus, the bundle of filaments is passed axially through the jet in the same direction as the air usually travels, the cross-sectional area of the bundle being, however, considerably less than thev cross-sectional area of the throat of the venturi, while the gas is delivered under pressure to that inlet of the jetv into which the water is usually fed. The details of design of one suitable jet are shown in the drawings and discussed below.
For best results, the gas fed to the jet should be heated to increase the evaporation of swelling liquid which occurs as the bundle passes through and beyond the jet. However, since in most jets the filaments will be under tension at some point in the jet, due to the force of the gas stream, and since crimping takes place when the swelling liquid is removed from the filaments while they are in substantially separated, tensionless condition, too great a degree of evaporation in the jet may interfere with the crimping tendency. Generally, it is desirable that the filaments emerge from the jet in an uncrimped, swollen condition, and that crimping take place after the filaments have left the jet.
The further evaporation of the swelling liquid, and the resulting crimping of the separated untensioned continuous filaments, may be effected continuously by conveying the parallel separated filaments in a stream of Patented Oct. 9, 1962` heated air or other gas and in substantially tensionless condition, until sufiicient swelling liquid is removed. In this case, the crimping occurs while the separated filaments are fioating in the gas stream. This crimping is not dependent on any turbulent flow of the carrying stream, and, in fact, gross turbulence, which would tend to entangle filaments or cause snarls or loopiness, is undesirable and is preferably avoided by suitable shielding to avoid drafts or other outside influences during drying. Thus, the stream carrying the filaments may pass through a tunnel or a long chute so constructed as to minimize turbulence. After the filaments have dried sufficiently to set the crimp firmly therein, they are brought together on a suitable collection device. Thus, they may pass through the nip of a pair of driven takeup rolls for delivery to a packaging device, such as the tow-packaging device shown in the copending application of Weber et al. Serial No. 262,856, filed December 21, 1951, now Patent No. 2,798,348. Since both evaporation and crimping :and the degree to which the fibers of the bundle are disarranged from a parallel orientation result in a differential reduction of the length of the filament bundle, the take-up rolls should be driven at such a speed that the rate of movement of the filaments at said rolls is less than the peripheral speed of the feed roll.
In another method of evaporating the swelling agent with the filaments in substantially tensionless, separated condition, the separated filaments leaving the air jet are allowed to fall freely onto a slowly moving porous belt or other conveying means which is passed through a drying zone. The filaments should be deposited on the belt, which may be in the form of an endless screen, in such a manner that there is a minimum of contact or crossing-over of filaments and therefore a minimum of interaction between adjacent filaments during the period when the filaments are crimping spontaneously, though some contact is permissible and generally unavoidable. It is convenient to lay the voluminous bundle of filaments onto belt back-and-forth across the belt, in a sinuous configuration. In this case, at the edges of the belt, in the sections where the bundle of filaments changes direction, the filaments tend to develop slightly less crimp than in the intermediate portions of the belt Where the bundle of filaments is generally straight and where the bundle is looser. This effect may be reduced by directing the hot air, used for drying the filaments, upwardly in a gentle stream through the pores of the belt; this makes for a more effective relaxation and separation of the filaments on the belt. Preferably the force of the stream of hot air is not great enough to actually lift the bundle of filaments from the belt.
The extent of separation of the filaments need not be great so long as they are kept substantially independent of each other. Thus, in one case, in which a bundle of 1400 swollen filaments, the average denier per filament being 3 (on a dry basis), were passed through an air jet to separate the filaments, the diameter of the bundle leaving the air jet was 3A; inch; in this case, by calculation, the average distance between adjacent filaments was on the order of 700-800 microns.
The extent of removal of liquid from the separated, untensioned filaments should be such that the filaments are brought to a substantially unswollen condition. For example, in the application of this invention to wetspinning of cellulose triacetate in a methylene chloridemethanol, spin bath, -it is preferable to continue the drying, while the filaments are separated and untensioned, until the liquid content is reduced to about or less, based on the weight of the cellulose triacetate.
The crimping obtained in accordance with this invention is not dependent on the use of high temperatures during removal of the liquid. Thus, in the preferred form of the invention (involving wet-spinning of cellulose triacetate in a methylene chloride-methanol spin bath), it is desirable to feed air at a temperature in the range of about 70 to 140 C. to the jet, but good results have been obtained using air at room temperature for this purpose. Even when hot air at 1407 C. is fed to the jet, the temperature of the air leaving the jet with the filaments is probably in the neighborhood of 50 C., due to cooling resulting from evaporation of methanol and methylene chloride. In the same process, air at a temperature of about to 90 C. has been supplied to the drying zone where the crimping of the filaments occurs, but here again the actual temperature of the filaments during the time crimping takes place is probably less than 65 C.
yIt is advantageous to apply a textile lubricant to the filaments. This lubricant is best applied after the removal of liquid from the filaments, that is, when the filaments are in non-swollen condition. The lubricant, which may, for example, be that described in United States Patent No. 2,805,992, 4issued to Fortess et al. on September 10, 1957, is conveniently supplied -by passing the unswollen filaments over a roller, carrying a film of lubricant, before the filaments are engaged in the nip of the take-up rolls. More desirably, a mist of the lubricant may be applied by a suitable spraying device at this Ipoint. The application of lubricant in the form of a -rnist or spray results in a more uniform distribution of lubricant throughout the bundle and avoids the development of tension which would result from passage of the bundle over a lubricating roller or other surface under such conditions as to secure uniformity of application.
The process of this invention is especially vaiuable for the production of a crimped tow, made up of a thousand or more continuous filaments and having a total denier of 3000 or more, the denier per filament being about 1 to 6. It has previously been the general practice to crimp tow mechanically, as by passing the tow through a suitable heated stufiing box type of crimper. Such mechanical crimping damages the individual filaments of the tow, particularly when a highly crimped material, having five or more crimps per inch, is produced. In addition, when mechanical crimping is employed, the crimps in all the filaments of the tow are aligned and more or less in the same plane. In contrast, when the method of the present invention is used, the filaments of the tow are not damaged at all. The crimps in adjacent filaments are randomly arranged, out of alignment; the crimp being three-dimensional, either helically or randomly threedimensional, and not substantially in a single plane. Thus, the tow is much more voluminous or lofty than the conventional tows. When the tow produced in accordance with this invention is cut into staple ber lengths and then processed in the conventional manner to produce staple fiber yarn, much less breakage of filaments and formation of undesirable short filaments or fly takes place. Also, because of the voluminous character of the material, much less mechanical processing is necessary to open or separate the staple fibers before they are formed into yarns.
Typical crimped filaments produced in accordance 'with this invention contain 8 or more e.g. 8 to l2, fine crimps per inch, the amplitude of the crimp being irregular but generally being on the order of 1 mm. and the percent crimp, based on the straightened length, being above about 4%. Percent crimp is defined as Straightened length-crimped length Straightened length ferred to above, the use of certain critical proportions of methylene chloride in the spin bath results in the production of filamentary materials of outstanding physical properties (e.g. tenacity of at least 1.8 grams per denier and elongation of at least 18%). In the practice of the present invention it is preferable to use proportions of methylene chloride within the scope of the Riley application. lt is found however, that if the proportion of methylene chloride in the spin bath is decreased below the critical level and the proportion of methanol increased (for example by 2%, based on the weight of the bath, above the critical level), there is a greater tendency for the formation of crimped filaments, though the physical properties of the filaments are not as good. Preferably, the proportions of methylene chloride in the spin bath are within the range defined by the formula where C is the concentration in percent and T is the temperature in C.
By the process of this invention there are obtained crimped cellulose triacetate filamentary materials whose mechanical properties are superior to those of any crimped filaments obtained by the wet, dryor melt-spinning of cellulose triacetate. Thus, there are obtained crimped filamentary materials whose tenacity is at least 1.8, usually above 2, grams per denier and whose elongation is at least 18%, usually above 20%, even for filaments whose denier is in the range of 1.5 to 4. The energy of rupture, i.e. the area under the stress-strain curve from zero stretch to break, is high. These crimped filamentary materials are characterized by radial uniformity. This can be determined by treating the filamentary materials with a saponifying agent which deesterifies the surface portions of the filamentary material, forming a cellulose skin which is then removed with a solvent for cellulose. When subjected to this treatment a filamentary material which is non-uniform exhibits different properties as compared with the original material, while a radially uniform material has the same properties as before.
ln testing for radial uniformity the surface removal can be effected, for example, by wetting the filaments to be tested in cold water containing 0.1 gram per liter of Triton X-l (iso-octyl phenyl ether of polyethylene glycol) then immersing them in 1000 times their weight of a 50 grams per liter solution of sodium hydroxide at 95 C. for from 30 seconds to 3 minutes, and quickly transferring them to cold running water for minutes. The filaments are then soured in acetic acid for minutes and again rinsed in running water for l5 minutes. After drying in air, the filaments are immersed at room temperature for 3 minutes in a solution made up of equal weights of cupriethylene diamine and lwater to dissolve the cellulose skin formed by the saponication. The filaments are then rinsed, soured, rinsed and dried as before.
The foregoing treatments of course reduce the filament denier but the tenacity in grams per denier is not changed. The percent elongation also remains unchanged. X-ray diffraction patterns, microscopic observations and other properties are also the same for the starting material and for specimens from which `surface layers of different thickness are removed. The safeironing temperature following heat treatment is also the same whether or not the filament is de-surfaced.
Whereas surface removal of dry spun cellulose triacetate eects a marked increase in the rate of dyeing, surface removal of crimped cellulose triacetate filamentary material wet spun in accordance with the present invention does not similarly affect the dyeing rate. This is demonstrated as follows: Dry spun cellulose triacetate filaments of 3.75 denier when immersed in a dyebath took up `0.18% of their weight of dyestuf after being immersed in the dyebath for 5 minutes and 0.22% of their weight after 15 minutes immersion. If these fila- 6 ments are first treated as described to remove a surface layer 44x10-6 cm. thick, the filaments under identical dyeing conditions will pick up 0.22% by weight of dyestuff in 5 minutes and 0.30% in 15 minutes. This appreciable increase in pick up evidences radial heterogeneity in the filaments.
By way of comparison, 2.5 denier filaments produced in accordance with the invention pick up 0.24% by weight of dyestuff after being immersed 5 minutes in the dyebath previously set forth Iand 0.34% after 15 minutes. Removal of a surface layer 47x10'6 cm. thick does not increase the dyeing rate. Actually there is a slight decrease to 0.23% and 0.31% in 5 and l5 minutes, respectively, i.e. approximately the same rate as de-surfaced dry spun cellulose triacetate filaments. This slight decrease in the dyestuff pick up rate of de-surfaced wet spun filaments produced in accordance with the present invention as opposed to wet spun filaments which have not been de-surfaced is due to the fact that the wet spun filaments initially have a slightly pebbled 4surface which is smoothed out upon de-surfacing thereby reducing slightly the surface to volume ratio of the filaments.
In the above tests the dyebath was water containing 50 grams per liter of dispersed Amacel Red 2B (a red cellulose acetate dye), 1 gram per liter of Igepon T-Sl (a dispersing agent) and l gram per liter of sodium hexametaphosp'hate; the bath was maintained at C.
The filamentary materials of this invention show a relatively high overall birefringence after complete saponification (according to the technique described below) of said materials. The overall birefringence of the saponified material is above about 0.031, typical values being in the range of about 0.034 to 0.037. This overall birefringence is the sum of the birefringences through the fiber and is measured, in conventional manner, by a transmission technique. In the complete saponificatio-n method ernployed for this purpose, the filamentary material is saponified completely by immersion for at least 3() minutes in times its weight of a solution containing, by weight, 5 parts of sodium hydroxide, 12 parts of sodium acetate, 10 parts of dimethylsulfoxide land 73 parts of lwater, at 80 C. Completion of saponication can be checked by wetting the filamentary material with l-N cupriethylene diamine solution; if, as viewed under a microscope, the filamentary material dissolves completely in 30 seconds, saponification is complete; if not complete, the time of immersion in the s-aponifying liquor can be increased. When it has been determined that saponiliication is complete, the filamentary material is rinsed with distilled water until the rinse water is neutral. The saponified material is air dried. The treatment does not cause shrinkage or loss of strength. The overall birefningence, as opposed to merely surface birefringence, is determined in customary manner, as with a Berek compensator using polarized light.
Cellulose triacetate filamentary materials produced in accordance Iwith this invention exhibit definite rubbery properties at elevated temperatures. This is demonstrated in the following manner: A denier 40 filament yarn is held at constant length r(eg. 10 inches) and heated to a temperature of 220 C. `at a just perceptible initial tension (about 0.03 g.). The temperature is then cycled between 217 C. and 223 C. It will be found that the tension on the filament increases as the temperature increases and decreases very perceptibly as the temperature decreases, typical of a rubber. By Way of comparison, if the temperature of the filament is cycled between 162 C. and 168 C., the tension will be found to decrease as the temperature increases, typical of a glass.
Like other cellulose triacetate filamentary material, the cellulose triacetate filamentary material obtained in accordance with this invention may be heat treated to raise the safe ironing -tempenature of fabrics produced therefrom and to improve the dimensional stability, resistance to creasing, permanence of pleating, and the like. However, the filamentary matenial of this invention shows substantially no shrinkage or decrease of tenacity on such heat treatment. In fact, the tenacity may even increase. For example, a filament produced in accordance with this invention and having an original tenacity of 2.15 grams per denier, when heat treated in lair at 210 C. for minutes shrinks fless than 1% and has a final tenacity of 2.37 g./den.
Cellulose triacetate filamentary material produced in accordance with the invention is also charatcerized by resistance to creep yat elevated temperature. This is demonstrated as follows: One end of la filament is anchored within a lhorizontal heating tube. inches from the anchored end, the filament is knotted to a glass lament which extends outside the tube and runs over a pulley. A weight is suspended from the protruding end of the glass filament. glass filament the tube is heated `and the displacement of the weight with change in temperature is noted. Cellulose triacetate filaments produced by idry spinning the initial solutions begin to creep at about 168 C. The instant filamentary materials do not creep comparably below `about 178-183 C. The rate `and amount of creep for dryspun filaments under a lo-ad of 0.033 gram per denier are only reached for the instant ilamentary materials at a load equal to or in excess of 0.067 gram per denier.
While the invention has been described in connection with cellulose triacetate as the filament-forming mtaterial, it may be 'applied to other organic-solvent soluble filament-forming materials; e.g. to cellulose nitrate or other cellulose esters.
In the accompanying drawing, which illustrates some aspects of this invention,
FIG. 1 illustnates, diagrammatically, the process of this invention.
FIGS. 2 and 3 'are two views of a modiiication of the drying and crimping stage of the process,
FIG. 4 is a cross-sectional view of an air jet, drawn to scale, as indicated,
FIG. 5 is an enlarged photograph of la crimped tow produced in accordance with this invention, yand 'also showing an individual crimped lament, alongside said tow.
FIG. 6 is a photograph showing the cross-section of a crimped tow produced according to this invention, showing the circular cross-sections of the individual filaments.
FIG. 7 is a photomicrograph of the single filament of FIG. 5, the filament being tensioned suiiiciently to pull out the crimp temporarily land being shadowed with chromium to show the pebbled surface configuration. Like reference numerals designate like parts in the several views of the drawing.
In the drawing reference numeral 11 designates a spinnerette mounted in suitable vessel 12 filled with spin bath liquid which is supplied to said vessel by a pump 13. The `spin bath liquid enters the vessel through a sparger 14, passing through a layer of metallic wool 16 to reduce turbulence. The spin bath also lills a vertical spin column 17 which communicates with the vessel 12 and whose tapered lower end 18 is positioned directly above and surrounds the spinnerette 11. A spinning solution, or dope, is forced by the action of a pump 19 through the apertures of the spinnerette 11 and into the spin bath to form filaments 21, which are drawn upward through the spin column 17, and over a pulley 22, by the action of a driven feed roll 23. The spin bath, which moves slowly up the spin column 17, fiows over a weir 24 to a catch basin 26, from which it is withdrawn and, after purification, recirculated to the vessel 12 through the pump 13. Some of the spin bath liquid adheres to the filaments leaving the column 17; part of this adherent liquid is removed mechanically by suitable devices such as stripper guides 27 and vacuum strippers 28 engaged With various size weights suspended from the by the filamentsv as they pass to the feed roll 23. The still wet filaments, in the form of a bundle or tow make several wraps around the feed roll 23 and the usual idler roll 29 associated therewith and then are fed to a predrier 31, supplied with hot air. From the predrier 31 the tow passes through a horizontal air jet 32, where it is subjected to a stream of heated air and from which it emerges as a horizontal stream 33 of parallel separated filaments, supported in substantially tensionless condition in a stream of heated air passing through an enclosed drying zone .34. A long smooth horizontal chute 36; mounted just below the stream of air and out of contact with the filaments helps toI control the direction of air flow and to support the filaments in the air stream. The filament-s, now thoroughly dry and crimped, are passed under a sprayer 37, where a mist of textile lubricant is applied, and are then taken up as a continuous bundle by means of a pair of driven rolls 33 and 39. This bundle, or tow 41, is collected in any suitable manner, as in a container 42.
In the embodiment illustrated in FIGS. 2 and 3, the separated filaments 33 emerging from the jet 32 fall, under their own weight, through a pivoted traverse tube 46, to an endless moving screen 47, driven through rollers 48, which screen carries them through a drying oven 49. The ltraverse tube 46 is rocked on its pivot 51, by suitable mechanism 52, to distribute the filaments back and forth across :the width of the moving screen 47, and the rate of movement of the traverse tube and screen are so coordinated the loose bundle of filaments 53 is laid back and forth across the belt, successive traverses of the bundle being `side by side and not one on top of another.
As shown in FIG. 4 the jet 32 comprises a main body 56 having an axial venturi passage 57 and three circular side inlets 58, spaced evenly around the axis, for the introduction of compressed air into the entrance end 59 of said passage. Fitted axially within said entrance end 59 is a tapered yarn inlet tube 61, which terminates just before the throat 62 of said venturi passage 57. The yarn passes axially through the tube 61 while the air travels around said tube, the yarn and air moving together from the throat 61 to the wider discharge end of the venturi passage, and then out into the atmosphere. The jet 32 is symmetrical about its axis, all cross-sections at right angles to the axis being circular, except, of course, for the side inlets 58. FIG. 4 is drawn precisely to the scale shown thereon.
The following examples are given to illustrate this invention further.
Example I A solution containing 21.5% of cellulose tn'acetate of 61.5% acetyl value, calculated as acetic acid, and of intrinsic viscosity 2.0 (measured on cellulose regenerated, without degradation, from said cellulose triacetate) dissolved in a mixture of parts of methylene chloride and 10 parts of methanol, is extruded upward from a spinnerette having 1396 circular holes each 0.10 mm. in diameter into a spin bath containing 43.0% methylene chloride and 57.0% methanol at a temperature of 32 C. By the action of a feed roll mounted outside the spin bath the resulting filaments are drawn upward through a spin tube having a height of cm. and filled with the spin bath, the latter moving upward at the rate of about 14 meters per minute. The filaments emerging from the top of the spin column carry about 30G-400% of liquid, based on the weight of cellulose triacetate. The composition of this liquid is substantially the same as that of the spin-bath. On their way to the feed roll the wet filaments are brought together to form a tow and are passed successively over stripper guides, a pulley and a sucking roll, which remove some of the liquid, so that their liquid content is about 250% at the feed roll. The feed roll moves the wet tow at the rate of 50y meters per minute under a tension of 186 grams (measured at the 9 top of the column after the tow passes the stripper guides), the draw-down ratio being 6.6:1. The total denier (on a dry basis) of this 1396 filament tow is 4188. From the feed roll the tow passes through a predryer in the form of an air jet through which the tow passes axially and which is supplied with air at a temperature of 120 C. and a pressure of 50 p.s.i.g. at the rate of 7.6 s.c.f.m. (i.e. measured at 14.7 p.s.i.g. and 62 F.). This eiects a partial separation of the filaments and decreases the liquid content thereof to 210%. The still wet swollen iilaments emerging from the predryer pass directly to an air aspirator, constructed as shown in FIG. 4 and supplied with air at a temperature of 120 C. and an inlet pressure of 90 p.s.i.g. at the rate of 8.8 s.c.f.m. The resulting separated, parallel filaments containing 70% liquid, based on the weight of cellulose triacetate, emerge horizontally from the jet and then fall onto an endless moving metallic screen, where they are dried in substantially tensionless and separated condition in air, the air being at a temperature of 70 C. and moving upwardlf,l through the screen, until their liquid content is reduced to less than 1%, after which a mist of lubricant is applied uniformly to the lilaments. The resulting tow is much more voluminous than mechanically crimped tow. The individual iilaments have 3-dimensional, irregular and sinusoidal crimps and have an amplitude of about 1 mm. and a frequency of about 10 crimps per inch. The percent crimp, based on the straightened length, is about 5.1%. The crimp is retained even when the filaments are strained past their yield point, with appreciable crimp being retained even after a strain of 5% is applied. The crimp is retained after washing in hot water (e.g. 70 C.). The individual laments, which are substantially circular in cross-section, have a tenacity at break of 1.8 grams per denier and an elongation at break (based on their uncrimped length) of 22%. When the tow is cut to form staple fibers 2 inches in length and the resulting bers are processed in the usual manner to form yarn, a strong yarn is formed easily, with practically no formation of fly.
Example II A solution containing 21.5% of cellulose triacetate of acetyl value 61.5%, based on acetic acid, dissolved in a mixture of 90 parts methylene chloride and 10 parts oft methanol, is forced through a spinnerette, having 40 circular holes each 0.1 mm. in diameter, into a spin bath containing 40% of methylene chloride and 60% methanol at a temperature of 33 C. and is taken up on a feed roll at the rate of 50 meters per minute, at a draw-down ratio of 6.611. The resulting wet 40iilament yarn, having a total denier (on a dry basis) of 120 is passed through an air aspirator supplied with air at p.s.i.g. and at a temperature of 22 C. 'I'he separated filaments emerging from the jet oat substantially horizontally on the air stream for a distance of 3 feet under substantially no tension until they are dry and are then taken up as a voluminous yarn, by means of a pair of driven rollers which move said yarn at the rate of 50 meters per minute. The individual laments of this yarn are almost perfect helices, the amplitude of the crimp being about 1 mm. at a frequency of 10 crimps per inch, and the resulting yarn is voluminous. The lilaments are substantially circular in cross-section.
It is to be understood that the foregoing detailed description is merely given by way of illustration and that many variations may be made therein without departing from the spirit of my invention.
Having described my invention, what I desire to secure by Letters Patent is:
1. A crimped tilamentary material of cellulose triacetate having a tenacity of at least 1.8 grams per denier, an elongation o-f at least 18% and a pebbled surface.
2. A crimped cellulose triacetate filament exhibiting a tenacity of at least 1.8 grams per denier, an elongation of at least 18%, a pebbled surface, radial uniformity, an overall birefringence above about 0.031 when completely sapOnied, rubbery properties at 220 C., resistance to creep at 168 C., and substantially no shrinkage on heat treatment.
3. A crimped lilamentary material of cellulose triacetate having a tenacity of about 1.8 grams per denier, an elongation of about 22% and a pebbled surface.
4. A crimped filamentary material of cellulose triacetate having a tenacity of about 1.8 to 2.15 grams per denier and an elongation of about 18% to about 22% and a pebbled surface.
5. A crimped lamentary material of cellulose triacetate having a denier below about 4, a tenacity of at least 1.8 grams per denier, an elongation of at least 18% and a pebbled surface.
References Cited in the tile of this patent UNITED STATES PATENTS 2,090,924 Whitehead Aug. 24, 1937 2,098,228 Clarke et al. Nov. 9, 1937 2,143,205 Mller et al Jan. l0, 1939 2,238,977 Jackson et al Apr. 22, 1941 2,537,312 Mehler Jan. 9, 1951 2,612,679 Lacisch Oct. 7, 1952 2,657,973 Johnson et al. Nov. 3, 1953 2,674,025 Ladisch Apr. 6, 1954 2,705,184 Drisch Mar. 29, 1955 2,732,279 Tachikawa Jan. 24, 1956 2,807,864 Head Oct. l, 1957 2,831,748 IFinlayson et a1. Apr. 22, 1958 2,862,284 Wiczer Dec. 2, 1958 2,869,318 Stucki Jan. 20, 1959 2,889,611 Bedell June 9, 1959
Claims (1)
1. A CRIMPED FILAMENTARY MATERIAL OF CELLULOSE TRIACETATE HAVING A TENACITY OF AT LEAST 1.8 GRAMS PER DENINER, N ELONGATION OF AT LEAST 28% AND A PEBBLED SURFACE.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US729980A US3057038A (en) | 1957-06-05 | 1958-04-21 | Wet spun cellulose triacetate |
| GB17159/58A GB881856A (en) | 1957-06-05 | 1958-05-29 | Crimped wet-spun filamentary materials |
| DEC16953A DE1291051B (en) | 1957-06-05 | 1958-06-04 | Process for the production of curled threads from cellulose esters |
| FR767294A FR1237720A (en) | 1957-06-05 | 1958-06-05 | Process for the production of filamentary materials and resulting products |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66381557A | 1957-06-05 | 1957-06-05 | |
| US729980A US3057038A (en) | 1957-06-05 | 1958-04-21 | Wet spun cellulose triacetate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3057038A true US3057038A (en) | 1962-10-09 |
Family
ID=27098824
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US729980A Expired - Lifetime US3057038A (en) | 1957-06-05 | 1958-04-21 | Wet spun cellulose triacetate |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3057038A (en) |
| DE (1) | DE1291051B (en) |
| FR (1) | FR1237720A (en) |
| GB (1) | GB881856A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3180785A (en) * | 1962-03-21 | 1965-04-27 | Kendall & Co | Synthetic fibers with increased surface friction |
| US3202747A (en) * | 1961-04-26 | 1965-08-24 | Celanese Corp | Method for crimping wet spun cellulose triacetate |
| US3258825A (en) * | 1962-03-26 | 1966-07-05 | Eastman Kodak Co | Methods for the production of highshrink modacrylic yarn |
| US3402446A (en) * | 1966-08-03 | 1968-09-24 | Owens Corning Fiberglass Corp | Apparatus for bulking yarn |
| US3486208A (en) * | 1965-01-22 | 1969-12-30 | Ici Ltd | Process for making woven stretch fabrics |
| US4587168A (en) * | 1984-04-05 | 1986-05-06 | Toyo Boseki Kabushiki Kaisha | Hollow fiber membrane for dialysis |
| US5462801A (en) * | 1993-07-09 | 1995-10-31 | Rhone-Poulenc Rhodia Aktiengesellschaft | Filter Tow, method for the production thereof, as well as tobacco smoke filter element and method for its production |
| US20100300468A1 (en) * | 2007-12-21 | 2010-12-02 | Rhodia Acetow Gmbh | Filter tow bale, method and device for producing a filter tow bale and filter tow strips |
| US20110011413A1 (en) * | 2007-12-21 | 2011-01-20 | Rhodia Acetow Gmbh | Filter tow strip, filter rod machine, method for producing filter tow strips and method for producing filter rods |
| WO2016124166A1 (en) * | 2015-02-06 | 2016-08-11 | 3T Textiltechnologie Transfer Gmbh | Method for feeding a staple-fiber sliver to a laying head, textile machine, and method for retrofitting a textile machine |
| EP3674455A1 (en) * | 2018-12-28 | 2020-07-01 | Lenzing Aktiengesellschaft | Process for liquid removal from cellulose filaments yarns or fibers |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2090924A (en) * | 1934-05-01 | 1937-08-24 | Celanese Corp | Artificial filament and method of making the same |
| US2098228A (en) * | 1931-03-04 | 1937-11-09 | Eastman Kodak Co | Artificial silk |
| US2143205A (en) * | 1933-02-15 | 1939-01-10 | Boehringer & Soehne Gmbh | Artificial silk |
| US2238977A (en) * | 1937-09-16 | 1941-04-22 | Eastman Kodak Co | Production of cellulose derivative cut staple fibers |
| US2537312A (en) * | 1948-03-17 | 1951-01-09 | Du Pont | High elongation yarn |
| US2612679A (en) * | 1950-10-23 | 1952-10-07 | Ladisch Rolf Karl | Filaments containing fillers |
| US2657973A (en) * | 1949-10-28 | 1953-11-03 | British Celanese | Process for wet-spinning cellulose triacetate |
| US2674025A (en) * | 1949-08-15 | 1954-04-06 | Texiclon Corp | Polymeric filaments |
| US2705184A (en) * | 1949-08-25 | 1955-03-29 | Textile & Chemical Res Company | Process for the production of rayon products |
| US2732279A (en) * | 1951-12-07 | 1956-01-24 | Shozo tachikawa | |
| US2807864A (en) * | 1954-06-24 | 1957-10-01 | Eastman Kodak Co | Composition and process for treating yarn |
| US2831748A (en) * | 1952-02-26 | 1958-04-22 | British Celanese | Process for melt spinning crimped filaments |
| US2862284A (en) * | 1953-05-04 | 1958-12-02 | Sol B Wiczer | Modified filament and method |
| US2869318A (en) * | 1954-06-08 | 1959-01-20 | Celanese Corp | Voluminous yarn |
| US2889611A (en) * | 1954-09-24 | 1959-06-09 | Berkley W Bedell | Treatment of nylon filaments |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE160896C (en) * | ||||
| CH153449A (en) * | 1929-12-31 | 1932-03-31 | Aceta Gmbh | Process for the production of synthetic threads by the dry spinning process. |
| CH175036A (en) * | 1933-02-15 | 1935-02-15 | Boehringer & Soehne Gmbh | Process for the production of artificial structures from cellulose esters. |
-
1958
- 1958-04-21 US US729980A patent/US3057038A/en not_active Expired - Lifetime
- 1958-05-29 GB GB17159/58A patent/GB881856A/en not_active Expired
- 1958-06-04 DE DEC16953A patent/DE1291051B/en active Pending
- 1958-06-05 FR FR767294A patent/FR1237720A/en not_active Expired
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2098228A (en) * | 1931-03-04 | 1937-11-09 | Eastman Kodak Co | Artificial silk |
| US2143205A (en) * | 1933-02-15 | 1939-01-10 | Boehringer & Soehne Gmbh | Artificial silk |
| US2090924A (en) * | 1934-05-01 | 1937-08-24 | Celanese Corp | Artificial filament and method of making the same |
| US2238977A (en) * | 1937-09-16 | 1941-04-22 | Eastman Kodak Co | Production of cellulose derivative cut staple fibers |
| US2537312A (en) * | 1948-03-17 | 1951-01-09 | Du Pont | High elongation yarn |
| US2674025A (en) * | 1949-08-15 | 1954-04-06 | Texiclon Corp | Polymeric filaments |
| US2705184A (en) * | 1949-08-25 | 1955-03-29 | Textile & Chemical Res Company | Process for the production of rayon products |
| US2657973A (en) * | 1949-10-28 | 1953-11-03 | British Celanese | Process for wet-spinning cellulose triacetate |
| US2612679A (en) * | 1950-10-23 | 1952-10-07 | Ladisch Rolf Karl | Filaments containing fillers |
| US2732279A (en) * | 1951-12-07 | 1956-01-24 | Shozo tachikawa | |
| US2831748A (en) * | 1952-02-26 | 1958-04-22 | British Celanese | Process for melt spinning crimped filaments |
| US2862284A (en) * | 1953-05-04 | 1958-12-02 | Sol B Wiczer | Modified filament and method |
| US2869318A (en) * | 1954-06-08 | 1959-01-20 | Celanese Corp | Voluminous yarn |
| US2807864A (en) * | 1954-06-24 | 1957-10-01 | Eastman Kodak Co | Composition and process for treating yarn |
| US2889611A (en) * | 1954-09-24 | 1959-06-09 | Berkley W Bedell | Treatment of nylon filaments |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3202747A (en) * | 1961-04-26 | 1965-08-24 | Celanese Corp | Method for crimping wet spun cellulose triacetate |
| US3180785A (en) * | 1962-03-21 | 1965-04-27 | Kendall & Co | Synthetic fibers with increased surface friction |
| US3258825A (en) * | 1962-03-26 | 1966-07-05 | Eastman Kodak Co | Methods for the production of highshrink modacrylic yarn |
| US3486208A (en) * | 1965-01-22 | 1969-12-30 | Ici Ltd | Process for making woven stretch fabrics |
| US3402446A (en) * | 1966-08-03 | 1968-09-24 | Owens Corning Fiberglass Corp | Apparatus for bulking yarn |
| US4587168A (en) * | 1984-04-05 | 1986-05-06 | Toyo Boseki Kabushiki Kaisha | Hollow fiber membrane for dialysis |
| US5462801A (en) * | 1993-07-09 | 1995-10-31 | Rhone-Poulenc Rhodia Aktiengesellschaft | Filter Tow, method for the production thereof, as well as tobacco smoke filter element and method for its production |
| US20110011413A1 (en) * | 2007-12-21 | 2011-01-20 | Rhodia Acetow Gmbh | Filter tow strip, filter rod machine, method for producing filter tow strips and method for producing filter rods |
| US20100300468A1 (en) * | 2007-12-21 | 2010-12-02 | Rhodia Acetow Gmbh | Filter tow bale, method and device for producing a filter tow bale and filter tow strips |
| WO2016124166A1 (en) * | 2015-02-06 | 2016-08-11 | 3T Textiltechnologie Transfer Gmbh | Method for feeding a staple-fiber sliver to a laying head, textile machine, and method for retrofitting a textile machine |
| EP3674455A1 (en) * | 2018-12-28 | 2020-07-01 | Lenzing Aktiengesellschaft | Process for liquid removal from cellulose filaments yarns or fibers |
| WO2020136109A1 (en) * | 2018-12-28 | 2020-07-02 | Lenzing Aktiengesellschaft | Process for liquid removal from cellulose filaments yarns or fibers |
| TWI725653B (en) * | 2018-12-28 | 2021-04-21 | 奧地利商藍晶股份公司 | Process for liquid removal from cellulose filaments yarns or fibers |
| CN113242917A (en) * | 2018-12-28 | 2021-08-10 | 连津格股份公司 | Method for removing liquid from cellulose filament yarn or fiber |
| KR20210102446A (en) * | 2018-12-28 | 2021-08-19 | 렌징 악티엔게젤샤프트 | Method for removing liquid from cellulosic filament yarns or fibers |
| JP2022515537A (en) * | 2018-12-28 | 2022-02-18 | レンチング アクチエンゲゼルシャフト | Cellulose filament The process of removing liquid from yarn or fibers |
| JP7140923B2 (en) | 2018-12-28 | 2022-09-21 | レンチング アクチエンゲゼルシャフト | Process for removing liquid from cellulose filament yarns or fibers |
| CN113242917B (en) * | 2018-12-28 | 2022-12-09 | 连津格股份公司 | Method for removing liquid from cellulosic filament yarns or fibres |
| US11873580B2 (en) | 2018-12-28 | 2024-01-16 | Lenzing Aktiengesellschaft | Process for liquid removal from cellulose filaments yarns or fibers |
Also Published As
| Publication number | Publication date |
|---|---|
| GB881856A (en) | 1961-11-08 |
| FR1237720A (en) | 1960-08-05 |
| DE1291051B (en) | 1969-03-20 |
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