US3018157A - Process of producing uniformly dyeing polyacrylonitrile filaments by heat stretching the water wetted filaments - Google Patents
Process of producing uniformly dyeing polyacrylonitrile filaments by heat stretching the water wetted filaments Download PDFInfo
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- US3018157A US3018157A US465355A US46535554A US3018157A US 3018157 A US3018157 A US 3018157A US 465355 A US465355 A US 465355A US 46535554 A US46535554 A US 46535554A US 3018157 A US3018157 A US 3018157A
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- 238000004043 dyeing Methods 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 53
- 229920002239 polyacrylonitrile Polymers 0.000 title description 10
- 229920001577 copolymer Polymers 0.000 claims description 12
- 239000003960 organic solvent Substances 0.000 claims description 6
- 238000000578 dry spinning Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- 239000000975 dye Substances 0.000 description 14
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 10
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 8
- 238000005470 impregnation Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 5
- 238000009736 wetting Methods 0.000 description 5
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000013557 residual solvent Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical class OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000002238 attenuated effect Effects 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000001046 green dye Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000009738 saturating Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000010936 aqueous wash Methods 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- -1 methyl acrylate Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- QIFCIFLDTQJGHQ-UHFFFAOYSA-M potassium;2-phenylethenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 QIFCIFLDTQJGHQ-UHFFFAOYSA-M 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Images
Classifications
-
- 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/38—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent
-
- 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
- Y10S8/93—Pretreatment before dyeing
Definitions
- This invention relates to an improved method of drawing acrylonitrile homopolymer and copolymer yarns, filaments and similar structures to produce attenuated products possessing greater uniformity of size and greater uniformity of dye receptivity.
- an object of this invention to provide an improved method for processing acrylonitrile polymer or copolymer yarns that have been initially collected as wound packages or which formed yarns contain nonuniformities that give rise to short length denier inequalities in the drawn yarn.
- Another object of this invention is to provide a yarn or filament conditioning step just prior to drawing that gives improved drawing uniformity from as spun yarn collected in package form as reflected by more uniform short length denier and greater dyeing uniformity of the drawn yarn or fabrics made therefrom.
- a still further object of this invention is to improve draw continuity by eliminating filament flaring due to static and subsequent filament strip-backs at the steam drawing cell.
- FIGURE 1 shows the application of the process of this invention to yarn on the run i.e., while moving rapidly;
- FIGURE 2 is a graph showing the uniformity in denier obtained by the process of this invention.
- FIGURE 3 shows graphically the non-uniformity that is normally obtained by prior art processes.
- the objects of this invention are accomplished by unwinding packaged yarn or filaments, uniformly wetting the unwound yarn or filaments with water or aqueous solution and then drawing in an atmosphere of steam. Most effectively this wetting of the yarn takes place while moving rapidly, but any condition that permits the yarn to uniformly imbibe a substantial quantity of water is effective as will be explained more fully hereinafter.
- the temperature of the aqueous material may vary widely as, for instance, from room temperature up to 100 C.
- the duration of application has little or no effect as long as the time is sufficient for uniform impregnation under the tension being imposed and may be as short as second or as long as 24 hours or more.
- the tension at the time of impregnation is uniformly applied to the yarns and is generally not very great.
- Pure water or water containing up to 10% of other soluble materials, such as a solvent, may be impregnated into the yarn.
- the various organic solvents disclosed in US. Patents 2,404,714 to 2,404,727 may be present in the bath.
- inorganic salts may be present such as calcium chloride, Zinc chloride and sodium thiocyanate, these salts being used in concentrated solutions as solvents or being used in wet spinning procedures.
- materials which are not solvents for the polymers such as alcohol, glycerol or acetone.
- the bath contains only vaporizable material and is preferably water.
- steam drawing is effected with low or atmos pheric pressure steam.
- the improvement in denier and dyeing uniformity is from to 200% and results from soaking a relaxed skein of package-washed yarn or by passing the yarn on the run through a few inches of water just prior to steam drawing. Yarns similarly processed but not subjected to this water wetting step before drawing fail to show this improvement. As-spun yarn which had not been subjected to any prior washing treatment also is improved in dyeing uniformity when passed through a water bath on the run prior to drawing. No improvement at all was realized by soaking the yarn package (after washing to remove residual solvent) for a period of two days in water at 30 C. and then steam drawing. Similarly extending the solvent extraction time, i.e. pressure washing with water, to 10 hours as compared with a normal extraction time of about 3%.
- Uniform room temperature water impregnation of the washed yarn gives a noticeable improvement in denier uniformity. However, greater improvement results as the temperature of the water treatment is increased above about 40 C. In some cases not only is short length dyeing uniformity more improved by higher temperature water impregnation but residual shrinkage of the yarn from various parts of the spin package is uniformized and yarn from the inside of the package and from the outside of the package may be used side-by-side without encountering the characteristic dye junctions frequently present.
- the invention is applicable to yarns, filaments and other attenuated structures of homopolymers of acrylonitrile and to copolymers containing a major portion of and preferably upwards of 85% acrylonitrile such as acrylonitrile copolymerized with monoethylenically or diethylenically unsaturated compounds as vinyl acetate, vinyl chloride, vinylidene chloride, methyl vinyl ketone, styrene, vinylpyridine, acrylic acid and its esters, such as methyl acrylate, ethylenesulfonates, l-propylenesulfonates, styrenesulfonates, and the like.
- acrylonitrile such as acrylonitrile copolymerized with monoethylenically or diethylenically unsaturated compounds as vinyl acetate, vinyl chloride, vinylidene chloride, methyl vinyl ketone, styrene, vinylpyridine, acrylic acid and its esters, such as methyl
- the copolymers may be comprised of two or three or more copolymerizing compounds such as 85% to 99% acrylonitrile and with or without minor amounts of other copolymerizable compounds.
- copolymers mixed polymers comprised of at least 85 acrylonitrile may be used.
- Useful polymers are given in many patents such as U.S. 2,404,714 through U.S. 2,404,727, U.S. 2,486,641 and others.
- the process of this invention comprises improving the physical properties and dyeability of a filament or yarn made from an acrylonitrile polymer by uniformly impregnating it with Water prior to drawing.
- the impregnation is done by contacting the filamentary material with an aqueous bath containing at least about 90% water and having a temperature from about room temperature to about 100 C., preferably about 40 C. to about 100 C.
- the extent of drawing is at least about 2 times the original length of the filaments, 2 to 10X usually being applied though greater drawing may be used if desired.
- the polymers are those containing at least 85% acrylonitrile for it is with these polymers that the optimum properties desired in the final textile articles, as for example, weather resistance, are obtained.
- water by itself is preferred.
- Example I A copolymer of 94% acrylonitrile and 6% methyl acrylate having an intrinsic viscosity of about 1.7 dissolved in N,N-dimethylformamide as a 25% solution was dry spun by the usual method and collected on a bobbin outside the spinning cell as 330 denier 30 filament yarn containing about 25% residual solvent. The yarn packages formed were subjected to pressure washing with 2% dimethylformamide aqueous wash liquor at 25 C. for 3.5 hours at the end of which time the dimethylformamide content of the yarn had been reduced to about 2% based on the dry yarn weight.
- FIG- URE 1 As schematically shown in the attached drawing (FIG- URE 1) the as spun packages of this yarn were placed on a creel 1 and unwound and drawn by means of two sets of a plurality of rolls 2 and 3.
- the drawing may be done as shown in U.S. Patent 2,568,920, the yarns being heated between roller sets 2 and 3.
- Yarns 4 were 'passed directly from the creel to the drawing unit while another set of yarns 5 was passed from the creel through four or five inches of water bath 6 at 25 C. (by means of a freely rotatable grooved roller gmide 7 submerged in the bath) and thence to the drawing apparatus.
- the tension on the yarn in the water bath was about 10 grams total which was only slightly more than the tension on Straight Loop Residual Denier Treatment T, g.p.d./E, T, g.p.d./E, Shrinkage, CDV, X
- the water dip had no appreciable effect on the drawn yarn properties with the exception of residual shrinkage which was increased slightly, but the coeflicient of denier variation was markedly aifected, being considerably lowered.
- FIGURE 2 The improvement in the short-length denier variation with the water dip which corresponds directly with the short-length dyeing non-uniformities in the drawn yarn is shown in FIGURE 2, where measurements on 200 consecutive 9-cm. lengths have been plotted. It will be noted that the sudden large fluctuations seen in the control (FIGURE 3) in yarn denier were greatly reduced. The average maximum periodic fluctuations in the untreated yarn were as large as 7 to 10% (short length section to section); the water dip treatment reduces these to about the 2 to 4% level. The periodicity of the large denier fluctuations corresponds to the distance of the yarn between the shoulders of the as spun package. Similar periodicity has been calculated for the shortlength dyeing non-uniformities as found in dyed knitted tubings.
- the intensity of the dyeing non-uniformity has been correlated directly to the degree of variation in shortlength denier.
- the dip treatment before draw is a simple, practical method for correcting these variations as they occur in the as spun package. This is illustrated in the following table:
- Example II Washed as spun yarn such as described in Example I was subjected to water dip treatment before drawing 5X in an atmospheric steam draw cell and relaxation of 10%.
- the water bath was heated to The C. dip as compared to the 40 C. dip reduced the residual shrinkage of the drawn yarn by about 18%.
- Tenacities of the 95 C. dip yarns were increased about 5%.
- Example III A homopolymer of acrylonitrile having an intrinsic viscosity of about 1.9 was dissolved in N,N-dimethylformamide and dry spun as 710 denier 40 filament yarn.
- the yarn from the spinning cell was suitably finished and collected with a small amount of twist on pirns.
- the pirns of yarn were pressured washed for 90 minutes to reduce the solvent content of the yarn to about 0.5% based on the dry yarn weight.
- Yarns from the same part of each washed package were drawn 4.5 X in the atmospheric steam draw cell immediately after one of three following conditioning steps: (1) no dip, (2) 40 C. water dip, and (3) 95 C. water dip.
- the drawn yarns were relaxed about to give a 180 denier drawn yarn.
- Example IV Four different terpolymers of acrylonitrile, methyl acry-- late and potassium styrenesulfonate were prepared under different conditions to give a range of molecular Weights as well as variations in composition. These polymers were dissolved in N,N-dimethylformamide and dry spun to a bobbin wind-up package, which was water extracted to free the yarn from solvent and the yarn was then drawn from 5 X to 6.5 X in atmospheric steam.
- Yarns from the same part of each washed package were drawn under three conditions. (1) No dip; (2) 40 C. dip; and (3) 95 C. dip. Uniformity of dyeing was compared on knitted tubings dyed with a basic green dye (Color Index No. 662). In all cases short length uniformity was improved with the dip treatment and the best results were obtained when the 95 C. dip was used.
- Example V Dye junctions between drawn yarn from the inside and from the outside cake windings of the as spun yarn can be substantially reduced or completely eliminated by a hot 95 C. dip treatment. For instance, when 8 spin cakes of yarn were preliminarily processed as described in Example 11 and given a water dip treatment at 40 C. prior to drawing 5 X the average in-out dye junction was 2.5 shades. When yarns from the same eight cakes were subjected to a 95 C. water dip just prior to drawing 5 no visible in-out dye junctions could be found. Thus, while water dip at any temperature just prior to drawing improves short length denier variations only at elevated temperatures such as 80 C. and above is there also a visible effect on in-out dye junctions.
- Example VI A copolymer of the same composition as described in Example I was processed as shown in Example I, except that the as-spun bobbin was not pressure washed.
- the yarn was passed through the water dip at 25 C. before drawing 5X in steam at 3 p.s.i.g., the short length dyeing uniformity of the yarn in knitted tubing was markedly improved.
- Similar yarns from the same as-spun package when drawn without the water dip were very non-uniform when dyed. In both instances substantial amounts (l0-11%) of residual solvent remained after this treatment. Longer contact times within the water trough are used if the beneficial effects of water dipping prior to drawing as Well as extraction are desired.
- the process for the production of a filament having improved dyeing properties and being capable of being drawn at least two times which comprises dry spinning a solution in an inert organic solvent of a copolymer having at least an acrylonitrile content and up to 15% of an ethylenically unsaturated monomer copolymen'zed therewith, winding the as-spun filament into a package, extracting the organic solvent from the filament while on the package with water, unwinding and saturating the said filament containing not more than about 2% of the aforesaid organic solvent with water by passing it under low uniform tension insufi'icient to produce appreciable permanent stretching through an aqueous medium inert to the said filament and in which the polymer is insoluble, and immediately thereafter drawing the resulting wet filament at least 2 times its original length in an atmosphere of low pressure steam.
- the process for the production of a filament having improved dyeing properties and being capable of being drawn at least two times which comprises dry spinning a solution in an inent organic solvent of a copolymer having at least 85% acrylonitrile content and up to 15% of an ethylenically unsaturated monomer copolymerized therewith, wind-ing the as-spun filament into a package, unwinding and saturating the said filament with water by passing it under low uniform tension through an aqueous bath inert to the said filament 7 and in which the polymer is insoluble, and drawing the 2,328,125 resulting wet filament at least 2 times its original length 2,346,208 in an atmosphere of low pressure steam.
- 2,394,540 2,404,714 References Cited in the file of this patent 5 2,420,565 UNITED STATES PATENTS 2,568,920
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- Chemical & Material Sciences (AREA)
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- General Chemical & Material Sciences (AREA)
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- Artificial Filaments (AREA)
Description
Jam 23, 1962 F. J. KOVARIK ETAL 3,018,157 PROCESS OF PRODUCING UNIFORMLY DYEING POLYACRYLONITRILE FILAMENTS BY HEAT STRETCHING THE WATER WETTED FILAMENTS Filed Oct. 28', 1954 Q 4 F] g. 1
A /\Y v I so 1 1 m 78 f/ 2 l\/\ l 76 Q V\/ 1 Y so so I00 I20 140 I I 200 CONSECUTIVE DENIER SAMPLES II. E Z LU Q 20 40 so 80 I00 I20 I40 I60 I80 200 INVENTORS CONSECUTIVE DENI ER SAM PLES FRANK JOSEPH KOVARIK CARL ERNEST LATSCHAR BY W ATTORNEY Patented Jan. 23, 1962 3 018 157 PROCESS OF PRODUOING UNIFORIVILY DYElNG POLYACRYLONITRILE FILAMENTS BY HEAT STERETSCHING THE WATER WETTED FILA- M NT Frank J. Kovarik and Carl Ernest Latschar, Waynesboro, Va., assignors to E. I. du Pont de Nemours 8: Company, Wilmington, Del., a corporation of Delaware Filed Oct. 28, 1954, Ser. No. 465,355 6 Claims. (Cl. 1854) This invention relates to an improved method of drawing acrylonitrile homopolymer and copolymer yarns, filaments and similar structures to produce attenuated products possessing greater uniformity of size and greater uniformity of dye receptivity.
As spun acrylonitrile polymer yarns and the like must be drawn a substantial amount to impart desirable physical properties to them. But, when the yarn from a dry spinning cell is wound up on a bobbin and the residual solvent is extracted by means of aqueous liquor while the yarn is still in package form, unwinding of the yarn, after drying or without drying, and steam drawing it from 2x to X, leads to undesirable fluctuations in short length denier measurements. Acrylonitrile polymer yarns when so produced and so processed also exhibit poor dyeing uniformity which has given rise to much research in an eifort to eliminate these non-uniformities.
It is, therefore, an object of this invention to provide an improved method for processing acrylonitrile polymer or copolymer yarns that have been initially collected as wound packages or which formed yarns contain nonuniformities that give rise to short length denier inequalities in the drawn yarn. Another object of this invention is to provide a yarn or filament conditioning step just prior to drawing that gives improved drawing uniformity from as spun yarn collected in package form as reflected by more uniform short length denier and greater dyeing uniformity of the drawn yarn or fabrics made therefrom. A still further object of this invention is to improve draw continuity by eliminating filament flaring due to static and subsequent filament strip-backs at the steam drawing cell. Other objects will be apparent from the description that follows.
In the figures:
FIGURE 1 shows the application of the process of this invention to yarn on the run i.e., while moving rapidly;
FIGURE 2 is a graph showing the uniformity in denier obtained by the process of this invention; and
FIGURE 3 shows graphically the non-uniformity that is normally obtained by prior art processes.
The objects of this invention are accomplished by unwinding packaged yarn or filaments, uniformly wetting the unwound yarn or filaments with water or aqueous solution and then drawing in an atmosphere of steam. Most effectively this wetting of the yarn takes place while moving rapidly, but any condition that permits the yarn to uniformly imbibe a substantial quantity of water is effective as will be explained more fully hereinafter. The temperature of the aqueous material may vary widely as, for instance, from room temperature up to 100 C. The duration of application has little or no effect as long as the time is sufficient for uniform impregnation under the tension being imposed and may be as short as second or as long as 24 hours or more. The tension at the time of impregnation is uniformly applied to the yarns and is generally not very great. Pure water or water containing up to 10% of other soluble materials, such as a solvent, may be impregnated into the yarn. The various organic solvents disclosed in US. Patents 2,404,714 to 2,404,727 may be present in the bath. Also, inorganic salts may be present such as calcium chloride, Zinc chloride and sodium thiocyanate, these salts being used in concentrated solutions as solvents or being used in wet spinning procedures. There may be present also materials which are not solvents for the polymers such as alcohol, glycerol or acetone. Normally, the bath contains only vaporizable material and is preferably water. Preferably steam drawing is effected with low or atmos pheric pressure steam.
That uniform impregnation of the yarn with an aqueous medium just prior to drawing produces unexpectedly and surprisingly good uniformity of short length denier and of dyeing is borne out by a number of varied experiments. All evidence points to the necessity of substantially uniform water take-up by the yarn, and, therefore, the tension and/or pressure on the yarn must be substantially uniform throughout its entire length during the wetting treatment. Apparently, the as spun package of yarn or any other relatively dense package structure has too tight a structure or there are variations in the tension on the yarn so that uniform take-up of water throughout the length of the yarn is prevented. In the process of this invention the yarn is free to imbibe water readily, for it is in the form of a running yarn or a loose skein.
The improvement in denier and dyeing uniformity is from to 200% and results from soaking a relaxed skein of package-washed yarn or by passing the yarn on the run through a few inches of water just prior to steam drawing. Yarns similarly processed but not subjected to this water wetting step before drawing fail to show this improvement. As-spun yarn which had not been subjected to any prior washing treatment also is improved in dyeing uniformity when passed through a water bath on the run prior to drawing. No improvement at all was realized by soaking the yarn package (after washing to remove residual solvent) for a period of two days in water at 30 C. and then steam drawing. Similarly extending the solvent extraction time, i.e. pressure washing with water, to 10 hours as compared with a normal extraction time of about 3%. hours gave no improvement in denier nor in dyeing uniformity. Furthermore, skeins of yarn unwound from the water-washed package and allowed to hang free for a period of time before drawing yielded a non-uniform dyeing, drawn yarn as did yarn processed directly from the package.
From these and other experiments it is apparent that uniform water wetting of acrylonitrile polymer and copolymer yarns substantially improves short length denier uniformity and dyeing uniformity. Water analyses of washed package yarn and yarn removed from the package and impregnated with water while free to readily imbibe it shows that the water content is very substantially increased by this latter step. Based on the dry weight of the yarn the average water content of the washed yarn removed from the spin package is about 40% while the content of the yarn unwound from the package and thereafter impregnated with water is about 100% by weight.
Uniform room temperature water impregnation of the washed yarn gives a noticeable improvement in denier uniformity. However, greater improvement results as the temperature of the water treatment is increased above about 40 C. In some cases not only is short length dyeing uniformity more improved by higher temperature water impregnation but residual shrinkage of the yarn from various parts of the spin package is uniformized and yarn from the inside of the package and from the outside of the package may be used side-by-side without encountering the characteristic dye junctions frequently present.
The invention is applicable to yarns, filaments and other attenuated structures of homopolymers of acrylonitrile and to copolymers containing a major portion of and preferably upwards of 85% acrylonitrile such as acrylonitrile copolymerized with monoethylenically or diethylenically unsaturated compounds as vinyl acetate, vinyl chloride, vinylidene chloride, methyl vinyl ketone, styrene, vinylpyridine, acrylic acid and its esters, such as methyl acrylate, ethylenesulfonates, l-propylenesulfonates, styrenesulfonates, and the like. The copolymers may be comprised of two or three or more copolymerizing compounds such as 85% to 99% acrylonitrile and with or without minor amounts of other copolymerizable compounds. In place of copolymers, mixed polymers comprised of at least 85 acrylonitrile may be used. Useful polymers are given in many patents such as U.S. 2,404,714 through U.S. 2,404,727, U.S. 2,486,641 and others.
Thus, the process of this invention comprises improving the physical properties and dyeability of a filament or yarn made from an acrylonitrile polymer by uniformly impregnating it with Water prior to drawing. The impregnation is done by contacting the filamentary material with an aqueous bath containing at least about 90% water and having a temperature from about room temperature to about 100 C., preferably about 40 C. to about 100 C. The extent of drawing is at least about 2 times the original length of the filaments, 2 to 10X usually being applied though greater drawing may be used if desired. Preferably, the polymers are those containing at least 85% acrylonitrile for it is with these polymers that the optimum properties desired in the final textile articles, as for example, weather resistance, are obtained. Of the many media which may be used, water by itself is preferred.
The following examples illustrate this invention further and are given without any intention of being limited thereby.
Example I A copolymer of 94% acrylonitrile and 6% methyl acrylate having an intrinsic viscosity of about 1.7 dissolved in N,N-dimethylformamide as a 25% solution was dry spun by the usual method and collected on a bobbin outside the spinning cell as 330 denier 30 filament yarn containing about 25% residual solvent. The yarn packages formed were subjected to pressure washing with 2% dimethylformamide aqueous wash liquor at 25 C. for 3.5 hours at the end of which time the dimethylformamide content of the yarn had been reduced to about 2% based on the dry yarn weight.
As schematically shown in the attached drawing (FIG- URE 1) the as spun packages of this yarn were placed on a creel 1 and unwound and drawn by means of two sets of a plurality of rolls 2 and 3. The drawing may be done as shown in U.S. Patent 2,568,920, the yarns being heated between roller sets 2 and 3. Yarns 4 were 'passed directly from the creel to the drawing unit while another set of yarns 5 was passed from the creel through four or five inches of water bath 6 at 25 C. (by means of a freely rotatable grooved roller gmide 7 submerged in the bath) and thence to the drawing apparatus. The tension on the yarn in the water bath was about 10 grams total which was only slightly more than the tension on Straight Loop Residual Denier Treatment T, g.p.d./E, T, g.p.d./E, Shrinkage, CDV, X
percent percent percent percent N0 Dip 2. 87/16. 7 2. 51/14. 4 5. 9 2. 7 78. 4 Dip (25 0.)... 2. 86/161 2. 48/13. 8 6.1 1.9 78. 2
CDVeoefiicient 01 denier variation of 25 consecutive 9-cm. lenths. X-average denier.
Advantageously, the water dip had no appreciable effect on the drawn yarn properties with the exception of residual shrinkage which was increased slightly, but the coeflicient of denier variation was markedly aifected, being considerably lowered.
The improvement in the short-length denier variation with the water dip which corresponds directly with the short-length dyeing non-uniformities in the drawn yarn is shown in FIGURE 2, where measurements on 200 consecutive 9-cm. lengths have been plotted. It will be noted that the sudden large fluctuations seen in the control (FIGURE 3) in yarn denier were greatly reduced. The average maximum periodic fluctuations in the untreated yarn were as large as 7 to 10% (short length section to section); the water dip treatment reduces these to about the 2 to 4% level. The periodicity of the large denier fluctuations corresponds to the distance of the yarn between the shoulders of the as spun package. Similar periodicity has been calculated for the shortlength dyeing non-uniformities as found in dyed knitted tubings.
The intensity of the dyeing non-uniformity has been correlated directly to the degree of variation in shortlength denier. The dip treatment before draw is a simple, practical method for correcting these variations as they occur in the as spun package. This is illustrated in the following table:
5X Drawn Intensity of Dyeing Barre Treatment Yams- ODV (200) Greatest No Dip 3. 4 Improved Dip 25 0..... 2. 0 Intermediate. No Dip 3. 3 Improved.. Dip 25 O 2.1 Best N0 Dip 2.3 Improved Dip 25 C..." 2.0
Example II Washed as spun yarn such as described in Example I was subjected to water dip treatment before drawing 5X in an atmospheric steam draw cell and relaxation of 10%. In this example the water bath was heated to The C. dip as compared to the 40 C. dip reduced the residual shrinkage of the drawn yarn by about 18%. Tenacities of the 95 C. dip yarns were increased about 5%.
Example III A homopolymer of acrylonitrile having an intrinsic viscosity of about 1.9 was dissolved in N,N-dimethylformamide and dry spun as 710 denier 40 filament yarn.
The yarn from the spinning cell was suitably finished and collected with a small amount of twist on pirns. The pirns of yarn were pressured washed for 90 minutes to reduce the solvent content of the yarn to about 0.5% based on the dry yarn weight. Yarns from the same part of each washed package were drawn 4.5 X in the atmospheric steam draw cell immediately after one of three following conditioning steps: (1) no dip, (2) 40 C. water dip, and (3) 95 C. water dip. The drawn yarns were relaxed about to give a 180 denier drawn yarn.
Uniformity of dyeing was compared with three types of dyes on knitted tubings made from these yarns; a basic green dye (Color Index No. 662), and acid blue dye (Foreign Prototype 12) applied by the cuprous-ion dyeing technique, and a blue dispersed dye (Foreign Prototype 62). In all cases the no-dip items exhibited ex treme short-length dyeing nonuniformities whereas the 40 C. and 95 C. water dip yarns dyed substantially uniformly. With all the classes of dyes the water dip increased the dye shade and dyeing rates. For example, the basic dye rate for the water-dip yarns was increased about 40% as compared to the no-dip yarn.
Example IV Four different terpolymers of acrylonitrile, methyl acry-- late and potassium styrenesulfonate were prepared under different conditions to give a range of molecular Weights as well as variations in composition. These polymers were dissolved in N,N-dimethylformamide and dry spun to a bobbin wind-up package, which was water extracted to free the yarn from solvent and the yarn was then drawn from 5 X to 6.5 X in atmospheric steam.
Yarns from the same part of each washed package were drawn under three conditions. (1) No dip; (2) 40 C. dip; and (3) 95 C. dip. Uniformity of dyeing was compared on knitted tubings dyed with a basic green dye (Color Index No. 662). In all cases short length uniformity was improved with the dip treatment and the best results were obtained when the 95 C. dip was used.
Example V Dye junctions between drawn yarn from the inside and from the outside cake windings of the as spun yarn can be substantially reduced or completely eliminated by a hot 95 C. dip treatment. For instance, when 8 spin cakes of yarn were preliminarily processed as described in Example 11 and given a water dip treatment at 40 C. prior to drawing 5 X the average in-out dye junction was 2.5 shades. When yarns from the same eight cakes were subjected to a 95 C. water dip just prior to drawing 5 no visible in-out dye junctions could be found. Thus, while water dip at any temperature just prior to drawing improves short length denier variations only at elevated temperatures such as 80 C. and above is there also a visible effect on in-out dye junctions.
Characterization of the drawn yarns leading to in-out dye junctions has shown a strong correlation between residual shrinkage and dye shade, particularly for the 200/ 80 denier counts. Deep dye shades and increased dye rates are closely associated with high residual shrinkages. In the following table the average residual shrinkages for 44 cakes shows the effectiveness of the 95 C. dip in uniformizing in-out shrinkage variations for drawn 75 denier 30 filament yarn.
RESIDUAL SHRINKAGE Similar improvements have been obtained with other copolymers and with the terpolymers of Example IV.
Example VI A copolymer of the same composition as described in Example I was processed as shown in Example I, except that the as-spun bobbin was not pressure washed. In the case where the yarn was passed through the water dip at 25 C. before drawing 5X in steam at 3 p.s.i.g., the short length dyeing uniformity of the yarn in knitted tubing was markedly improved. Similar yarns from the same as-spun package when drawn without the water dip were very non-uniform when dyed. In both instances substantial amounts (l0-11%) of residual solvent remained after this treatment. Longer contact times within the water trough are used if the beneficial effects of water dipping prior to drawing as Well as extraction are desired.
Similar experiments with the water dip were not effective when the unextracted as-spun yarns were drawn in high pressure steam (40 p.s.i.).
By the easily applied treatment of this. invention short length denier uniformity and dyeing uniformity is greatly improved. The uniform and substantially complete impregnation of the as-spun yarn with water assists in overcoming a tendency for static to build up on the yarns undergoing drawing and as the result there is no filament flaring when these water-dipped yarns are drawn. 'Ihis noticeably improves the quality of the drawn yarn and the continuity of drawing. By employing high temperature water dip not only are the short length dyeings uniformized but dye junctions between the inside and outside yarn from the spin package are greatly reduced or completely eliminated.
Any departure from the above description which conforms to the present invention is intended to be included within the scope of the claims.
We claim:
1. The process for the production of a filament having improved dyeing properties and being capable of being drawn at least two times which comprises dry spinning a solution in an inert organic solvent of a copolymer having at least an acrylonitrile content and up to 15% of an ethylenically unsaturated monomer copolymen'zed therewith, winding the as-spun filament into a package, extracting the organic solvent from the filament while on the package with water, unwinding and saturating the said filament containing not more than about 2% of the aforesaid organic solvent with water by passing it under low uniform tension insufi'icient to produce appreciable permanent stretching through an aqueous medium inert to the said filament and in which the polymer is insoluble, and immediately thereafter drawing the resulting wet filament at least 2 times its original length in an atmosphere of low pressure steam.
2. The process of claim 1 in which the polymer is polyacrylonitrile.
3. The process of claim 1 in which the polymer is a terpolymer of acrylonitrile, methyl acrylate and a styrenesulfonate.
4. The process of claim 1 in which the aqueous medium has a temperature of from about room temperature to C.
5. The process of claim 1 in which the aqueous medium has a temperature between about 40 C. to 100 C.
6. The process for the production of a filament having improved dyeing properties and being capable of being drawn at least two times which comprises dry spinning a solution in an inent organic solvent of a copolymer having at least 85% acrylonitrile content and up to 15% of an ethylenically unsaturated monomer copolymerized therewith, wind-ing the as-spun filament into a package, unwinding and saturating the said filament with water by passing it under low uniform tension through an aqueous bath inert to the said filament 7 and in which the polymer is insoluble, and drawing the 2,328,125 resulting wet filament at least 2 times its original length 2,346,208 in an atmosphere of low pressure steam. 2,394,540 2,404,714 References Cited in the file of this patent 5 2,420,565 UNITED STATES PATENTS 2,568,920
2,226,529 Austin Dec. 31, 1940 2,278,896 Rugeley Apr. 7, 1942 2,285,552 Alfthan June 9, 1942 10 603.
8 Buchsbaurn Aug. 31, 1943 Conaw ay Apr. 11, 1944 Finzel Feb. 12, 1946 Latham July 23, 1946 Ru-geley et a1 May 13, 1947 Kinraide Sept. 25, 1951 OTHER REFERENCES Textile Research Journal, July 1954, pages 597 and
Claims (1)
1. THE PROCESS FOR THE PRODUCTION OF A FILAMENT HAVING IMPROVE DYEING PROPERTIES AND BEING CAPABLE OF BEING DRAWN AT LEAST TWO TIME WHICH COMPRISES DRY SPINNING A SOLUTION IN AN INERT ORGANIC SOLVENT OF A COPOLYMER HAVING AT LEAST AN 85% ARYLONITRILE CONTENT AND UP TO 15% OF AN ETHYLENICALLY UNSATURATED MONOMER COPOLYMERIZED THEREWITH, WINDING THE AS-SPUN FILAMENT
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US465355A US3018157A (en) | 1954-10-28 | 1954-10-28 | Process of producing uniformly dyeing polyacrylonitrile filaments by heat stretching the water wetted filaments |
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US465355A US3018157A (en) | 1954-10-28 | 1954-10-28 | Process of producing uniformly dyeing polyacrylonitrile filaments by heat stretching the water wetted filaments |
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Cited By (2)
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US3925524A (en) * | 1972-06-22 | 1975-12-09 | Celanese Corp | Process for the production of carbon filaments |
US4066731A (en) * | 1976-04-14 | 1978-01-03 | Mobil Oil Corporation | Method of making polymeric acrylonitrile films |
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US2226529A (en) * | 1937-11-10 | 1940-12-31 | Du Pont | Synthetic filament |
US2278896A (en) * | 1938-12-06 | 1942-04-07 | Carbide & Carbon Chem Corp | Composite material |
US2285552A (en) * | 1940-07-25 | 1942-06-09 | Du Pont | Production of filaments |
US2328125A (en) * | 1940-02-17 | 1943-08-31 | Buchsbaum & Company S | Method for making filaments |
US2346208A (en) * | 1941-04-08 | 1944-04-11 | Du Pont | Treatment of high tenacity yarn of synthetic origin |
US2394540A (en) * | 1943-08-20 | 1946-02-12 | Du Pont | Stretching of artificial yarn |
US2404714A (en) * | 1942-06-17 | 1946-07-23 | Du Pont | Polymer products |
US2420565A (en) * | 1943-02-20 | 1947-05-13 | Carbide & Carbon Chem Corp | Synthetic textile articles |
US2568920A (en) * | 1949-04-21 | 1951-09-25 | Du Pont | Apparatus for treating shaped articles with fluids |
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Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
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US2226529A (en) * | 1937-11-10 | 1940-12-31 | Du Pont | Synthetic filament |
US2278896A (en) * | 1938-12-06 | 1942-04-07 | Carbide & Carbon Chem Corp | Composite material |
US2328125A (en) * | 1940-02-17 | 1943-08-31 | Buchsbaum & Company S | Method for making filaments |
US2285552A (en) * | 1940-07-25 | 1942-06-09 | Du Pont | Production of filaments |
US2346208A (en) * | 1941-04-08 | 1944-04-11 | Du Pont | Treatment of high tenacity yarn of synthetic origin |
US2404714A (en) * | 1942-06-17 | 1946-07-23 | Du Pont | Polymer products |
US2420565A (en) * | 1943-02-20 | 1947-05-13 | Carbide & Carbon Chem Corp | Synthetic textile articles |
US2394540A (en) * | 1943-08-20 | 1946-02-12 | Du Pont | Stretching of artificial yarn |
US2568920A (en) * | 1949-04-21 | 1951-09-25 | Du Pont | Apparatus for treating shaped articles with fluids |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US3925524A (en) * | 1972-06-22 | 1975-12-09 | Celanese Corp | Process for the production of carbon filaments |
US4066731A (en) * | 1976-04-14 | 1978-01-03 | Mobil Oil Corporation | Method of making polymeric acrylonitrile films |
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