US2828528A - Finishing polyester fabrics - Google Patents
Finishing polyester fabrics Download PDFInfo
- Publication number
- US2828528A US2828528A US627743A US62774356A US2828528A US 2828528 A US2828528 A US 2828528A US 627743 A US627743 A US 627743A US 62774356 A US62774356 A US 62774356A US 2828528 A US2828528 A US 2828528A
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- US
- United States
- Prior art keywords
- fabric
- fabrics
- heat
- calendering
- roll
- 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
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- 239000004744 fabric Substances 0.000 title claims description 158
- 229920000728 polyester Polymers 0.000 title description 10
- 238000000034 method Methods 0.000 claims description 16
- -1 POLYETHYLENE TEREPHTHALATE Polymers 0.000 claims description 12
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 10
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 10
- 238000009998 heat setting Methods 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 3
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 238000003490 calendering Methods 0.000 description 28
- 239000003518 caustics Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000000523 sample Substances 0.000 description 14
- 238000011282 treatment Methods 0.000 description 14
- 239000000835 fiber Substances 0.000 description 10
- 230000004580 weight loss Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 238000010276 construction Methods 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000010903 husk Substances 0.000 description 4
- 239000008149 soap solution Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000009991 scouring Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- 229920001634 Copolyester Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 229910052977 alkali metal sulfide Inorganic materials 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- IBBQVGDGTMTZRA-UHFFFAOYSA-N sodium;2-sulfobenzene-1,3-dicarboxylic acid Chemical compound [Na].OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O IBBQVGDGTMTZRA-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06Q—DECORATING TEXTILES
- D06Q1/00—Decorating textiles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/04—Polyester fibers
Definitions
- a fabric comprising polyester yarns is calendered at elevated temperature and pressure and then treated with an aqueous solution of an inorganic alkaline material until there is a fabric weight loss of at least 5%.
- a fabric woven from polyethylene terephthalate yarns is calendered at a temperature of 100 F.-450 F. under a pressure of from about 0.12 tons per linear inch to about 2 tons per linear inch, followed by subjecting the fabric to dry heat while it is partially relaxed at a temperature of from about 250 F. to about 450 F.
- an alkaline material such as an alkali metal hydroxide or alkali metal salt derived from a weak acid or an alkaline earth metal hydroxide to produce a fabric weight loss of 5%25%.
- the purpose of the calendering step is to flatten the fabric surface and as a result of this treatment the cross section of the fibers of the fabric is deformed.
- the calendered fabric also has a noticeable chintz-like glaze on the surface.
- the temperature should be in the range of 100 F.450 F. and preferably 100 F.-350 F.
- Pressure on the fabric surface should be maintained in the range of 0.12 ton per linear inch to 2 tons per linear inch, and preferably between about 0.2 and about 0.8 ton per linear inch. Rate of the calendering depends on the temperature and pressure employed and the results desired in the particular fabric being treated.
- the fabric is calendered at between about and about 100 yards per minute.
- Fabric construction Will also affect the properties of the finished fabric. It will be obvious to those skilled in the art that the proper fabric construction must be chosen in order to obtain the particular body and handle desiredin the finished fabric. 7
- a further object is roll.
- the fabric surface must be deformed uniformly throughout its area by contacting at least 50% of the surface area of the fabric with calender rolls. This may be accomplished using either a standard smooth surfaced, highly polished stainless steel calender roll, which compresses and deforms of the fabric surface area, or a Schreiner roll which is a steel roll having many fine lines per inch engraved hit, and which, depending upon the number of lines, will compress about 50% or more of the fabric surface during calendering. Failure to deform at least 50% of the fabric area during calendering produces fabrics which are deficient in surface cover and dryness.
- a Schreiner or smooth calender roll is normally complemented by a standard hard smooth paper covered husk roll contacting the other side of the fabric in order to obtain the necessary amount of pressure against the fabric surface.
- the calendering step in this invention should not leave any pattern, visible to the unaided eye, on either fabric surface.
- the deformation'of the fabric is obtained on only one surface at a time in contrast to embossing rolls which contact and compress both sides of the fabric and leave a defined visible pattern on both surfaces.
- embossed fabrics lack the surface dryness and cover obtainable by this invention.
- the finished fabric When in the calendering treatment temperatures approaching 450 F. are employed, the finished fabric retains too much plastic-like handle unless excessive caustic treatment follows the heat treating step.
- the fabric After calendering, the fabric is subjected to dry heat at a temperature of 250 F. 450 F. for a period of time sufficient to heat-set the fabric in order to obtain optimum drape and liveliness.
- the fabric may be either relaxed or unrelaxed.
- the fabric is heatset if the fabric is treated in at least a partially relaxed condition at the above temperature for a time sufficlent to permit shrinkage of at least 3% Warpwise and 3% fillingwise or treated the same number of minutes at the same temperature in an unrelaxed condition.
- the time required for heat-setting the fabric under unrelaxed (not free to shrink) conditions is the time in minutes required to heat-set the same fabric at the same temperature under relaxed (free to shrink condition).
- the fabric is partially relaxed during heat treatment so as to allow the fabric to shrink somewhat in the warp and filling.
- Heat treatment under at least partially relaxed conditions results in higher liveliness, surfajce'dryness and drape and less threadiness in the finished fabrics than is obtained in fabrics that are heat-set unrelaxed according to the process of this invention. In some are generally not as good as with a separate heat t'reatf ment step.
- the fabric is hydrolyzed to'remove part or all of. the glaze orplastic like handle produced on the surface of the fabric by calendering, as well as to generally improve the fabric handle.
- This step in the process further modifies the cross-section of the component fibers by preferentially dissolving part of the. fiber surface, thereby accentuating the deformed cross-section. produced by the cal'endering step, which introduces random high and low points in the surface of. the fiber cross-section.
- Hydrolysis may be carried out by treating the fabric with an aqueous medium containing inorganic alkaline material capable of producing a weight loss in this step of at least Preferably this weight loss is held to a minimum, e. g., 5%25%, depending upon the type and construction, of fabric employed, in order to keep the process economical. However, in certain instances where it is desired to produce extremely high drape and liveliness in the final fabric, the weight loss may be extended to as much as 50%.
- Suitable alkaline materials include sodium hydroxide, which is preferred because of its availability and low cost, potassium hydroxide, and salts thereof derived from weak acids, said salts being characterized by a pH of at least 12 in 0.1 N aqueous solution.
- useful salts include alkali metal sulfides, alkali metal sulfites, alkali metal phosphates and alkali metal silicates.
- suitable inorganic alkaline materials include calcium hydroxide, barium hydroxide, strontium hydroxide and the like.
- Concentration of the alkaline material in the aqueous hydrolysis bath is preferably at least 2% based upon the bath weight. Concentration of alkaline material, the fabric exposure time in the bath, and the temperature of the hydrolysis bath may be varied at will to produce the desired weight loss in the fabric. Normally it is convenient to immerse the fabric in an aqueous solution of the desired alkaline material and to have the bath at or near normal boiling temperature at atmospheric pressure. In some cases it may be desirable to employ lower temperatures and longer times. Hydrolysis reduces the size of the yarn to a finer denier than that in the original fabric.
- the fabric After hydrolysis the fabric is generally rinsed with water, scoured with a dilute aqueous acid wash, and rinsed again, to remove any residual alkaline material remaining. The fabric then is dried at ordinary temperatures, usually at 200 F.240 F.
- the process of this invention has. been de scribed with respect to treating fabrics composed of polyethylene terephthalate yarns, it should be understood that the invention is likewise applicable to improving the handle of fabrics made from other polyester and copolyester yarns.
- the yarns will be composed of polyesters in which at least 90% of the recurring structural units are ethylene terephthalate units, with any residues present comprising other dicarboxylic acids or other glycols.
- the ethylene terephthalate copolyester may contain residues of sebacic acid, isophthalic acid, sodium sulfoisophthalic acid, or butylene glycol.
- the fabrics finished by this invention may be composed of yarns prepared from fibers and filaments having odd cross-sections, for example, in the shape of ribbon, dogbone, cruciform, Y-shaped, and the like, as well as the conventional circular cross-section.
- Woven fabrics of this invention are composed of at least 50% by weight of polyester fibers or filaments. That is, the fabrics may be made from blends of polyester fibers with other synthetic and natural fibers, providing the fabric is free from wool and other components which would be deleteriously affected by the caustic treating step in the process.
- Other fibers that may be blended, plied, and twisted or otherwise mixed during weaving with polyester fibersin include those made from polyamides and polyurethanes and their copolymers, acrylic polymers and copolymers, cellulose derivatives such as cellulose acetate, regenerated cellulose, cotton and the like.
- Fabrics finished by the process of this invention exhibit a very desirable handle along with other improved properties. These fabrics exhibit improved drape and suppleness (which may be measured, for example, by flexural rigidity), improved surface dryness, increased surface friction, liveliness, and luster, improved resilience, increased surface cover and opaqueness, and reduced threadiness. In addition, the treatment reduces yarn shiftiness in the fabric. In many respects the finished fabrics appear like silk and have similar scroop and rustle.
- the process of this invention yields fabrics that have good handle and silk-like appearance in addition to good surface covering power and dryness which is unattainable in fabrics that have been heat-set and caustic treated without the combination with the preliminary calendering treatment.
- Examples of typical fabrics which may be processed by this invention includes taifetas, georgettes, sand-crepes, tissue-failles, foulards, broadcloths, batistes, light weight suitings, dress and blouse fabrics, shirtings, lingerie, and rainwear.
- flexural rigidity (which is a measure of the suppleness and drape of a fabric, the lower the value the better the drape) is measured by the hanging heart method originated by Pierce (Journal of the Tex tile Institute, 21, T377, 1930) and performed as. described by Hoifman and Beste in Textile Research Journal, XXI, No. 2, 66 (February, 1951).
- Contact covering power in percent (I which is a measure of the surface cover, is determined by measuring the effect of background color on the reflectance of the fabric when exposed to a light source.
- the refiectance values in the equation below are determined using a Photovolt Reflectometer, Model 610 (Photovolt Corporation):
- the coefficient of surface friction (which is-a measure of the surface dryness of the fabric, value the drier the fabric) is determined mula:
- e is the total contact angle in radians (the sum of the three angles formed by the suspended fabric as a result of its contact with the three probes)
- T5 is the weight in grams attached to the bottom of the suspended fabric.
- the surface friction is measured by using a modified Instron tensile tester.
- Thes tester is modified so that a movable probe is positioned in the same plane and in horizontal parallel'opposed relationship with two separated fixed probes, so that the movable probe can be advanced between the two fixed probes. All three probes are covered with samples of the test fabric. Preparatory to testing, a stationary weighted sample of the same test fabric is suspended vertically with the movable probe on one side and the fixed probes on the other.
- the movable probe is first advanced, pushing the suspended fabric between the two fixed probes and forming an angle in the suspended fabric at each line of contact with a probe.
- the cross head of the Instron tester is lowered, the three fabric covered probe surfaces,which are fixed spatially with respect to each other and which are in frictional contact with the suspended. fabric, are drawn along the length of the suspended stationary fabthe higherthe from the f01-..
- the fabric After heat setting, the fabric is immersed for five minutes in a boiling caustic solution containing 3% by weight of sodium hydroxide, the weight of the solution being about 50 times the weight of the fabric. ,The' caustic treated fabric is removed and rinsed with. warm water for five minutes, treated with 1% acetic acid for ten minutes, rinsed again with warm water for 5 minutes, and finally dried at about 225 F. The resultant fabric lost approximately 25% of its weight during the caustic treatment. The fabric now has a drier, livelier and a much more desirable silk-like handle than the original control fabric. Table I shows some physical characteristics of the fabric.
- the warp is made of 30 denier yarn, having 30 filament, 7 Z turns per inch, and the filling of 60 denier yarn, having 60 filament, 3.5 Z turns per inch.
- the fabric is taken from the loom, and scoured, dried and calendered, as in Example I. In this example, the fabric is not heat-set after calendering, as in the first example, but is treated in a caustic bath and rinsed as described in Example I.
- the treated fabric exhibits a much more desirable handle than the original control fabric as shown in Table II, and is silk-like.
- fabric and finishing treatment are the same as in Example I, except that during heat-setting, the fabric is completely relaxed (i. e., it is allowed to shrink to the maximum extent possible in the pin-tenter).
- Warpwise shrinkage is 6% and fillingwise shrinkage is
- the treated fabric exhibits a much more desirable and silk-like handlethan the original control fabric, as'sh'own
- fabric and finishing treatment are the same as in Example 1, except that a stainless-steel Schreiner roll is used instead of a smooth surfaced calender roll.
- the Schreiner roll contacts about 60% ofthe fabric surface during calendering.
- the treated fabric is silklike and exhibits a muchdrier surface handle than even the finished fabric obtained in Example I.
- EXAMPLE V Polyethylene terephthalate yarn having 34 filaments and a total denier of 70 is woven into a plain weave of 112 x 86 construction, weighing 1.83 ounces per square yard. This fabric after weaving is crab scoured at 212 F. with 2% soap solution and dried at 225 F. 'The dry fabric is calendered on a stainless steel Schreiner roll at 300 F. and 0.6 ton/linear inch pressure once on each side of the fabric. The fabric is backed up by a smooth hard paper covered husk roll. The Schreiner roll has 260 diagonal lines per inch at a 60 angle and contacts about 60% of the surface area of the fabric.
- Each lines cross-section represents an equilateral triangle having a dimension of 0.0037 inch on each side, while the crosssection of the Schreiner roll surface resembles that of a saw tooth.
- the fabric is cra scoured again at 212 F. and dried at 225 F. It is heat-set at dry dimensions (i. e., unrelaxed) at 440 F. for one minute, and then immersed in an aqueous solution containing 3% by weight sodium hydroxide at 212 F. for 90 minutes. The fabric is removed from the caustic solution, rinsed in water to remove excess alkali and dried at 215 F. The resulting fabric showed a weight loss of 19.7% in the caustic treating step.
- the finished fabric has good drape, suppleness, liveliness and cover, in
- control fabric in Table V was given a standard commercial finishing treatment involving scouring at 212 F. with 2% soap solution, drying at 225 F., and then heat setting by subjecting the fabric to dry heat at 360 F. for 45 seconds. It was not calendered or treated with caustic.
- EXAMPLE VI A spun yarn of 60 cotton count made from 65% polyethylene terephthalate fibers (1.2 denier per filament and 1.5 inches in length) and 35% cotton fibers is woven into a plain weave of 120 x 68 construction. This fab-' ric, after weaving, is crab scoured at 212 F. with 2% soap solution and dried at 215 F. The dry fabric is calendered on a stainless steel Schreiner roll at 275 F. once on each side of the fabric using 0.6 ton/linear inch pressure, using the same Schreiner roll as in Example V. The fabric is backed up by a smooth hard paper-covered husk roll. After calendering, the fabric is crab scoured again at 212 F., then dried at 215 F.
- the fabric is heat-set at dry dimensions (i; e. unrelaxed condition) at 440 F. for one minute, then treated with an aqueous solution containing 3% by weight sodium hydroxide at 212 F. for 60 minutes.
- the fabric is removed from the caustic solution and rinsed in water to remove excess alkali and then dried at 215 F.
- the resulting fabric showed a weight loss of 6.8% in the caustic treating step.
- the finished fabric has good drape, suppleness, liveliness, and cover.
- the fabric has improved uniformity (reduction in visible reed marks, reduction in unevenness of yarn bundle, and an over-all better appearance) in comparison with a fabric of equivalent construction which has been finished by a scour and heat-set treatment, but has had no calendering or caustic treatment.
- a process for treating a polyethylene terephthalate tween about 100 F. and 450 fabric which comprises deforming the fabric by means of compressive force applied to at least of the sur face area of the fabric and distributed uniformly over the entire surface area of the fabric at a temperature be- F., heat setting the fabric by subjecting it to dry heat at a temperature from about 250 F. to about 450 F. and then immersing the fabric in an aqueous alkaline solution until the fabric has lost at least 5% in weight, followed by washing and drying the fabric.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatment Of Fiber Materials (AREA)
Description
United States FINISHING PGLYES'I'ER FABRICS Navin J. Gajjar, Wilmington, Deb, assignor to E. 1. du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware No Drawing. Application December 12, 1956 Serial No. 627,743
Claims. (CI. 28-76) also known to heat-treat polyester fabrics prior to caustic treatment for the purpose of further improving fabric properties. Both of these known treatments improve drape and liveliness of polyester fabrics.
It is an object of this invention to provide polyester fabrics having improved aesthetics. to provide a new method of finishing said fabrics to improve their handle. Another object is to provide a method for producing a pattern-less fabric composed of polyethylene terephthalate yarns and having a handle resembling that of silk fabrics. Other objects will appear in the description which follows.
'In accordance with this invention a fabric comprising polyester yarns is calendered at elevated temperature and pressure and then treated with an aqueous solution of an inorganic alkaline material until there is a fabric weight loss of at least 5%. In a preferred embodiment a fabric woven from polyethylene terephthalate yarns is calendered at a temperature of 100 F.-450 F. under a pressure of from about 0.12 tons per linear inch to about 2 tons per linear inch, followed by subjecting the fabric to dry heat while it is partially relaxed at a temperature of from about 250 F. to about 450 F. until the fabric has shrunk at least 3% warpwise and at least 3% fillingwise and then subjecting the fabric to hydrolysis in the presence of an aqueous solution of an alkaline material such as an alkali metal hydroxide or alkali metal salt derived from a weak acid or an alkaline earth metal hydroxide to produce a fabric weight loss of 5%25%.
The purpose of the calendering step is to flatten the fabric surface and as a result of this treatment the cross section of the fibers of the fabric is deformed. The calendered fabric also has a noticeable chintz-like glaze on the surface. In order to accomplish the desired changes in the fabric by means of the calendering opera tion several variables must be controlled. First, the temperature should be in the range of 100 F.450 F. and preferably 100 F.-350 F. Pressure on the fabric surface should be maintained in the range of 0.12 ton per linear inch to 2 tons per linear inch, and preferably between about 0.2 and about 0.8 ton per linear inch. Rate of the calendering depends on the temperature and pressure employed and the results desired in the particular fabric being treated. Typically the fabric is calendered at between about and about 100 yards per minute. Fabric construction Will also affect the properties of the finished fabric. It will be obvious to those skilled in the art that the proper fabric construction must be chosen in order to obtain the particular body and handle desiredin the finished fabric. 7
One of the most important factors in the calendering operation is the nature of the surface of the calender A further object is roll. In order to achieve the most desirable results of this invention the fabric surface must be deformed uniformly throughout its area by contacting at least 50% of the surface area of the fabric with calender rolls. This may be accomplished using either a standard smooth surfaced, highly polished stainless steel calender roll, which compresses and deforms of the fabric surface area, or a Schreiner roll which is a steel roll having many fine lines per inch engraved hit, and which, depending upon the number of lines, will compress about 50% or more of the fabric surface during calendering. Failure to deform at least 50% of the fabric area during calendering produces fabrics which are deficient in surface cover and dryness. A Schreiner or smooth calender roll is normally complemented by a standard hard smooth paper covered husk roll contacting the other side of the fabric in order to obtain the necessary amount of pressure against the fabric surface.
In addition to compressing at least 50% of the fabric area the calendering step in this invention should not leave any pattern, visible to the unaided eye, on either fabric surface. The deformation'of the fabric is obtained on only one surface at a time in contrast to embossing rolls which contact and compress both sides of the fabric and leave a defined visible pattern on both surfaces. Moreover, because the finest patterned embossing rolls will not deform anywhere near 50% of the fabric area, embossed fabrics lack the surface dryness and cover obtainable by this invention.
When in the calendering treatment temperatures approaching 450 F. are employed, the finished fabric retains too much plastic-like handle unless excessive caustic treatment follows the heat treating step. In order to keep the caustic treatment at a minimum, and thereby reduce fabric weight'loss and cost, the fabric'may be scoured relaxed at the boil after calendering. After this additional scouring, the fabric is dried, heat-set, and treated with caustic. This alternative procedure removes any excessive plastic-like handle with only about 10% fabric weight loss instead of as much as 20%-35% weight loss in the case of certain types of fabrics which have not been scoured following calendering.
After calendering, the fabric is subjected to dry heat at a temperature of 250 F. 450 F. for a period of time sufficient to heat-set the fabric in order to obtain optimum drape and liveliness. In this heat treating step the fabric may be either relaxed or unrelaxed. The fabric is heatset if the fabric is treated in at least a partially relaxed condition at the above temperature for a time sufficlent to permit shrinkage of at least 3% Warpwise and 3% fillingwise or treated the same number of minutes at the same temperature in an unrelaxed condition. Thus the time required for heat-setting the fabric under unrelaxed (not free to shrink) conditions is the time in minutes required to heat-set the same fabric at the same temperature under relaxed (free to shrink condition). Preferably the fabric is partially relaxed during heat treatment so as to allow the fabric to shrink somewhat in the warp and filling. Heat treatment under at least partially relaxed conditions results in higher liveliness, surfajce'dryness and drape and less threadiness in the finished fabrics than is obtained in fabrics that are heat-set unrelaxed according to the process of this invention. In some are generally not as good as with a separate heat t'reatf ment step. p
After heat-setting, the fabric is hydrolyzed to'remove part or all of. the glaze orplastic like handle produced on the surface of the fabric by calendering, as well as to generally improve the fabric handle. This step in the process further modifies the cross-section of the component fibers by preferentially dissolving part of the. fiber surface, thereby accentuating the deformed cross-section. produced by the cal'endering step, which introduces random high and low points in the surface of. the fiber cross-section.
Hydrolysis may be carried out by treating the fabric with an aqueous medium containing inorganic alkaline material capable of producing a weight loss in this step of at least Preferably this weight loss is held to a minimum, e. g., 5%25%, depending upon the type and construction, of fabric employed, in order to keep the process economical. However, in certain instances where it is desired to produce extremely high drape and liveliness in the final fabric, the weight loss may be extended to as much as 50%. Suitable alkaline materials include sodium hydroxide, which is preferred because of its availability and low cost, potassium hydroxide, and salts thereof derived from weak acids, said salts being characterized by a pH of at least 12 in 0.1 N aqueous solution. Examples of useful salts include alkali metal sulfides, alkali metal sulfites, alkali metal phosphates and alkali metal silicates. Other suitable inorganic alkaline materials include calcium hydroxide, barium hydroxide, strontium hydroxide and the like.
Concentration of the alkaline material in the aqueous hydrolysis bath is preferably at least 2% based upon the bath weight. Concentration of alkaline material, the fabric exposure time in the bath, and the temperature of the hydrolysis bath may be varied at will to produce the desired weight loss in the fabric. Normally it is convenient to immerse the fabric in an aqueous solution of the desired alkaline material and to have the bath at or near normal boiling temperature at atmospheric pressure. In some cases it may be desirable to employ lower temperatures and longer times. Hydrolysis reduces the size of the yarn to a finer denier than that in the original fabric.
After hydrolysis the fabric is generally rinsed with water, scoured with a dilute aqueous acid wash, and rinsed again, to remove any residual alkaline material remaining. The fabric then is dried at ordinary temperatures, usually at 200 F.240 F.
Although the process of this invention has. been de scribed with respect to treating fabrics composed of polyethylene terephthalate yarns, it should be understood that the invention is likewise applicable to improving the handle of fabrics made from other polyester and copolyester yarns. Preferably the yarns will be composed of polyesters in which at least 90% of the recurring structural units are ethylene terephthalate units, with any residues present comprising other dicarboxylic acids or other glycols. For example, the ethylene terephthalate copolyester may contain residues of sebacic acid, isophthalic acid, sodium sulfoisophthalic acid, or butylene glycol. Furthermore, the fabrics finished by this invention may be composed of yarns prepared from fibers and filaments having odd cross-sections, for example, in the shape of ribbon, dogbone, cruciform, Y-shaped, and the like, as well as the conventional circular cross-section.
Woven fabrics of this invention are composed of at least 50% by weight of polyester fibers or filaments. That is, the fabrics may be made from blends of polyester fibers with other synthetic and natural fibers, providing the fabric is free from wool and other components which would be deleteriously affected by the caustic treating step in the process. Other fibers that may be blended, plied, and twisted or otherwise mixed during weaving with polyester fibersinclude those made from polyamides and polyurethanes and their copolymers, acrylic polymers and copolymers, cellulose derivatives such as cellulose acetate, regenerated cellulose, cotton and the like.
Fabrics finished by the process of this invention exhibit a very desirable handle along with other improved properties. These fabrics exhibit improved drape and suppleness (which may be measured, for example, by flexural rigidity), improved surface dryness, increased surface friction, liveliness, and luster, improved resilience, increased surface cover and opaqueness, and reduced threadiness. In addition, the treatment reduces yarn shiftiness in the fabric. In many respects the finished fabrics appear like silk and have similar scroop and rustle. The process of this invention yields fabrics that have good handle and silk-like appearance in addition to good surface covering power and dryness which is unattainable in fabrics that have been heat-set and caustic treated without the combination with the preliminary calendering treatment.
Examples of typical fabrics which may be processed by this invention includes taifetas, georgettes, sand-crepes, tissue-failles, foulards, broadcloths, batistes, light weight suitings, dress and blouse fabrics, shirtings, lingerie, and rainwear.
The following examples iliustrate specific embodiments of this invention. All parts and percentages are by weight unless otherwise indicated.
In the examples flexural rigidity (which is a measure of the suppleness and drape of a fabric, the lower the value the better the drape) is measured by the hanging heart method originated by Pierce (Journal of the Tex tile Institute, 21, T377, 1930) and performed as. described by Hoifman and Beste in Textile Research Journal, XXI, No. 2, 66 (February, 1951).
Contact covering power in percent (I Which is a measure of the surface cover, is determined by measuring the effect of background color on the reflectance of the fabric when exposed to a light source. The refiectance values in the equation below are determined using a Photovolt Reflectometer, Model 610 (Photovolt Corporation):
W B)( rW-Rrn) Rw-RB where R =Reflectance of fabric on black background in per:
cent. R =Refiectance of fabric on white background in percent. 7
The coefficient of surface friction (which is-a measure of the surface dryness of the fabric, value the drier the fabric) is determined mula:
where e is the total contact angle in radians (the sum of the three angles formed by the suspended fabric as a result of its contact with the three probes), and T5 is the weight in grams attached to the bottom of the suspended fabric. The surface friction is measured by using a modified Instron tensile tester. Thes tester is modified so that a movable probe is positioned in the same plane and in horizontal parallel'opposed relationship with two separated fixed probes, so that the movable probe can be advanced between the two fixed probes. All three probes are covered with samples of the test fabric. Preparatory to testing, a stationary weighted sample of the same test fabric is suspended vertically with the movable probe on one side and the fixed probes on the other. The movable probe is first advanced, pushing the suspended fabric between the two fixed probes and forming an angle in the suspended fabric at each line of contact with a probe. As the cross head of the Instron tester is lowered, the three fabric covered probe surfaces,which are fixed spatially with respect to each other and which are in frictional contact with the suspended. fabric, are drawn along the length of the suspended stationary fabthe higherthe from the f01-..
ricx The dynamic and staticforcesrequired to over come the friction between the suspended fabric and the covered probes are recorded on the Instron tester. These forces in grams are averaged and the average force reported as T in the formula above. 1
EXAMPLE I A continuous filament polyethylene terephthalate yarn, having 34 filaments and a total denier of 70, is woven into a plain weave fabric of 136 x 95 construction,
weighing 2.5ounces per square yard. This fabric is taken from the loom and scoured at 180 F. with 2% soap solution for two passes at a fabric speed of 2 yards per minutes. After scouring, thte fabric is dried at wet dimensions on a pin-tenter frame at 225 F. The fabric is calendered between a smooth stainless steel roll and a-smooth husk roll at 350 F., 0.5 ton/linear inch pressure and 25 yards per minute fabric speed. The fabric is heat-set on a pin-tenterat 440 F. for one minute exposure with 5% overfeed in warp direction and two inches under width. After heat setting, the fabric is immersed for five minutes in a boiling caustic solution containing 3% by weight of sodium hydroxide, the weight of the solution being about 50 times the weight of the fabric. ,The' caustic treated fabric is removed and rinsed with. warm water for five minutes, treated with 1% acetic acid for ten minutes, rinsed again with warm water for 5 minutes, and finally dried at about 225 F. The resultant fabric lost approximately 25% of its weight during the caustic treatment. The fabric now has a drier, livelier and a much more desirable silk-like handle than the original control fabric. Table I shows some physical characteristics of the fabric.
Table I A 2 x 2 twill foulard fabric of 264 x 102 construction, weighing approximately 1.8 ounces per square yard, is woven from polyethylene terephthalate filament yarn. The warp is made of 30 denier yarn, having 30 filament, 7 Z turns per inch, and the filling of 60 denier yarn, having 60 filament, 3.5 Z turns per inch. The fabric is taken from the loom, and scoured, dried and calendered, as in Example I. In this example, the fabric is not heat-set after calendering, as in the first example, but is treated in a caustic bath and rinsed as described in Example I.
The treated fabric exhibits a much more desirable handle than the original control fabric as shown in Table II, and is silk-like.
In this example, fabric and finishing treatment are the same as in Example I, except that during heat-setting, the fabric is completely relaxed (i. e., it is allowed to shrink to the maximum extent possible in the pin-tenter).
Warpwise shrinkage is 6% and fillingwise shrinkage is The treated fabric exhibits a much more desirable and silk-like handlethan the original control fabric, as'sh'own In this example, fabric and finishing treatment are the same as in Example 1, except that a stainless-steel Schreiner roll is used instead of a smooth surfaced calender roll. The Schreiner roll contacts about 60% ofthe fabric surface during calendering. The treated fabric is silklike and exhibits a muchdrier surface handle than even the finished fabric obtained in Example I.
Table IV Weight 7 Flexural Surface Fabric (Oz./Sq.Yd.) 'Rigidity Friction (mg. cm.)
Untreated Control (scoured)- 2.5 38.8 0.249 Example IV 1. 9 16. 1 0; 328
EXAMPLE V Polyethylene terephthalate yarn having 34 filaments and a total denier of 70 is woven into a plain weave of 112 x 86 construction, weighing 1.83 ounces per square yard. This fabric after weaving is crab scoured at 212 F. with 2% soap solution and dried at 225 F. 'The dry fabric is calendered on a stainless steel Schreiner roll at 300 F. and 0.6 ton/linear inch pressure once on each side of the fabric. The fabric is backed up by a smooth hard paper covered husk roll. The Schreiner roll has 260 diagonal lines per inch at a 60 angle and contacts about 60% of the surface area of the fabric. Each lines cross-section represents an equilateral triangle having a dimension of 0.0037 inch on each side, while the crosssection of the Schreiner roll surface resembles that of a saw tooth. After calendering, the fabric is cra scoured again at 212 F. and dried at 225 F. It is heat-set at dry dimensions (i. e., unrelaxed) at 440 F. for one minute, and then immersed in an aqueous solution containing 3% by weight sodium hydroxide at 212 F. for 90 minutes. The fabric is removed from the caustic solution, rinsed in water to remove excess alkali and dried at 215 F. The resulting fabric showed a weight loss of 19.7% in the caustic treating step. The finished fabric has good drape, suppleness, liveliness and cover, in
addition to the properties shown in Table V.
The control fabric in Table V was given a standard commercial finishing treatment involving scouring at 212 F. with 2% soap solution, drying at 225 F., and then heat setting by subjecting the fabric to dry heat at 360 F. for 45 seconds. It was not calendered or treated with caustic.
EXAMPLE VI A spun yarn of 60 cotton count made from 65% polyethylene terephthalate fibers (1.2 denier per filament and 1.5 inches in length) and 35% cotton fibers is woven into a plain weave of 120 x 68 construction. This fab-' ric, after weaving, is crab scoured at 212 F. with 2% soap solution and dried at 215 F. The dry fabric is calendered on a stainless steel Schreiner roll at 275 F. once on each side of the fabric using 0.6 ton/linear inch pressure, using the same Schreiner roll as in Example V. The fabric is backed up by a smooth hard paper-covered husk roll. After calendering, the fabric is crab scoured again at 212 F., then dried at 215 F. The fabric is heat-set at dry dimensions (i; e. unrelaxed condition) at 440 F. for one minute, then treated with an aqueous solution containing 3% by weight sodium hydroxide at 212 F. for 60 minutes. The fabric is removed from the caustic solution and rinsed in water to remove excess alkali and then dried at 215 F. The resulting fabric showed a weight loss of 6.8% in the caustic treating step. The finished fabric has good drape, suppleness, liveliness, and cover. In addition, the fabric has improved uniformity (reduction in visible reed marks, reduction in unevenness of yarn bundle, and an over-all better appearance) in comparison with a fabric of equivalent construction which has been finished by a scour and heat-set treatment, but has had no calendering or caustic treatment.
I claim:
1. A process for treating a polyethylene terephthalate tween about 100 F. and 450 fabric which comprises deforming the fabric by means of compressive force applied to at least of the sur face area of the fabric and distributed uniformly over the entire surface area of the fabric at a temperature be- F., heat setting the fabric by subjecting it to dry heat at a temperature from about 250 F. to about 450 F. and then immersing the fabric in an aqueous alkaline solution until the fabric has lost at least 5% in weight, followed by washing and drying the fabric.
2. The process of claim 1 in which the fabric is compressed by calendering at a temperature between about F. and 350 F. at a pressure of between about 0.12 ton and about 2 tons per linear inch.
'3. The process of claim 2 in which the aqueous solution contains an alkali metal hydroxide.
4. The process of claim 3 in which the fabric is 100% polyethylene terephthalate.
5. The process of claim 4 in which the alkali metal hydroxide is sodium hydroxide.
2,712,170 Phillips July 5, 1955 Knapp Feb. 12, 1957.
Claims (1)
1. A PROCESS FOR TREATING A POLYETHYLENE TEREPHTHALATE FABRIC WHICH COMPRISES DEFORMING THE FABRIC BY MEANS OF COMPRESSIVE FORCE APPLIED TO AT LEAST 50% OF THE SURFACE AREA OF THE FABRIC AND DISTRIBUTED UNIFORMLY OVER THE ENTIRE SURFACE ARE OF THE FABRIC AT A TEMPERATURE BETWEEN ABOUT 100*F. AND 450*F., HEAT SETTING THE FABRIC BY SUBJECTING IT TO DRY HEAT AT A TEMPERATURE FROM ABOUT 250*F. TO ABOUT 450*F. AND THEN IMMERSING THE FABRIC IN AN AQUEOUS ALKALINE SOLUTION UNTIL THE FABRIC HAS LOST AT LEST 5% IN WEIGHT, FOLLOWED BY WASHING AND DRYING THE FABRIC.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE563152D BE563152A (en) | 1956-12-12 | ||
US627743A US2828528A (en) | 1956-12-12 | 1956-12-12 | Finishing polyester fabrics |
GB38574/57A GB847147A (en) | 1956-12-12 | 1957-12-11 | Improvements in or relating to the finishing of polyester fabrics |
FR1192358D FR1192358A (en) | 1956-12-12 | 1957-12-11 | Process for finishing polyester fabrics |
DEP19830A DE1140170B (en) | 1956-12-12 | 1957-12-12 | Process for the production of non-embossed fabrics containing polyester fibers with improved properties |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US627743A US2828528A (en) | 1956-12-12 | 1956-12-12 | Finishing polyester fabrics |
Publications (1)
Publication Number | Publication Date |
---|---|
US2828528A true US2828528A (en) | 1958-04-01 |
Family
ID=24515939
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US627743A Expired - Lifetime US2828528A (en) | 1956-12-12 | 1956-12-12 | Finishing polyester fabrics |
Country Status (5)
Country | Link |
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US (1) | US2828528A (en) |
BE (1) | BE563152A (en) |
DE (1) | DE1140170B (en) |
FR (1) | FR1192358A (en) |
GB (1) | GB847147A (en) |
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2995803A (en) * | 1959-05-21 | 1961-08-15 | Haveg Industries Inc | Process of preparing heat-resistant glass fabric |
US3017685A (en) * | 1957-05-25 | 1962-01-23 | Heberlein Patent Corp | Process for the production of fabrics from specially prepared yarns |
US3096557A (en) * | 1961-01-03 | 1963-07-09 | Du Pont | Process for hot-wet calendering fabrics |
US3110617A (en) * | 1960-05-20 | 1963-11-12 | Du Pont | Textile |
US3111359A (en) * | 1959-10-16 | 1963-11-19 | Rohm & Haas | Modified textile and industrial fibers and fabrics and process for making them |
US3135577A (en) * | 1959-12-22 | 1964-06-02 | Ici Ltd | Process for improving the handle of polyethylene terephthalate fabrics with an alkali metal hydroxide and specific quaternary ammonium salts |
US3235426A (en) * | 1961-08-01 | 1966-02-15 | Du Pont | Method of rendering thermoplastic resins receptive to coatings |
US3245826A (en) * | 1963-06-12 | 1966-04-12 | Clevite Corp | Magnetic recording medium and method of manufacture |
US3287787A (en) * | 1960-09-30 | 1966-11-29 | Ici Ltd | Method of selectively weakening crimped polyester filaments and fibers |
US3302265A (en) * | 1964-04-21 | 1967-02-07 | Du Pont | Process for preparation of flannel fabrics from synthetic fibers |
US3731351A (en) * | 1970-10-12 | 1973-05-08 | Monsanto Co | Process of manufacturing tightly woven acrylic fabric |
US4008044A (en) * | 1975-06-03 | 1977-02-15 | J. P. Stevens & Co., Inc. | Treatment of polyester textiles to improve soil release and wettability properties |
US4270913A (en) * | 1979-07-06 | 1981-06-02 | Celanese Corporation | Pill-resistant polyester fabrics |
US4803256A (en) * | 1988-02-01 | 1989-02-07 | Dow Corning Corporation | Method of altering the surface of a solid synthetic polymer |
US4842792A (en) * | 1988-02-16 | 1989-06-27 | Eastman Kodak Company | Drafting process for preparing a modified polyester fiber |
US4872276A (en) * | 1988-05-13 | 1989-10-10 | Milliken Research Corporation | Calendering process for polyester fabric |
US4996107A (en) * | 1988-02-16 | 1991-02-26 | Eastman Kodak Company | Ink reservoir containing modified polyester fibers |
US5010663A (en) * | 1988-10-28 | 1991-04-30 | Stern & Stern Industries, Inc. | Low permeability fabric and method of making same |
US5075990A (en) * | 1986-09-11 | 1991-12-31 | International Paper Company | Battery separator fabric method for manufacturing |
US5124205A (en) * | 1988-02-16 | 1992-06-23 | Eastman Kodak Company | Ink reservoir containing modified polyester fibers |
EP0453678B1 (en) * | 1988-10-28 | 1995-01-11 | STERN & STERN INDUSTRIES, INC. | Low permeability fabric and method of making same |
WO2003080921A1 (en) * | 2002-03-25 | 2003-10-02 | Univerza V Ljubljani, Naravoslovnotehniska Fakulteta, Oddelek Za Tekstilstvo | PRETREATMENT METHOD OF POLyESTER FOR REDUCING ELIMINATION OF OLIGOMERS AT HIGH-TEMPERATURE ACID COLOURING WITH DISPERSION DYES |
US20150314326A1 (en) * | 2012-12-17 | 2015-11-05 | Kolon Glotech, Inc. | Method for manufacturing planarized fabric substrate for flexible display |
US20170370031A1 (en) * | 2014-12-25 | 2017-12-28 | Asahi Kasei Kabushiki Kaisha | Thin woven fabric having superior comfort |
US10227725B2 (en) * | 2014-04-16 | 2019-03-12 | Cummins Filtration Ip, Inc. | Tuning surface properties of melt blown polyester fibers by hydrolysis and solution grafting |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US2712170A (en) * | 1952-09-06 | 1955-07-05 | Goodyear Tire & Rubber | Treatment of textile fabrics |
US2781242A (en) * | 1954-02-05 | 1957-02-12 | Du Pont | Process of improving the hand of polyethylene terephthalate fabric by heat shrinking and hydrolyzing the fabric |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB652948A (en) * | 1948-08-13 | 1951-05-02 | John D Arcy Henry Hall | Improvements in textile materials |
GB748964A (en) * | 1952-07-31 | 1956-05-16 | Cilander Ag | An improved process of mechanically finishing sheet materials containing synthetic fibres |
-
0
- BE BE563152D patent/BE563152A/xx unknown
-
1956
- 1956-12-12 US US627743A patent/US2828528A/en not_active Expired - Lifetime
-
1957
- 1957-12-11 FR FR1192358D patent/FR1192358A/en not_active Expired
- 1957-12-11 GB GB38574/57A patent/GB847147A/en not_active Expired
- 1957-12-12 DE DEP19830A patent/DE1140170B/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2712170A (en) * | 1952-09-06 | 1955-07-05 | Goodyear Tire & Rubber | Treatment of textile fabrics |
US2781242A (en) * | 1954-02-05 | 1957-02-12 | Du Pont | Process of improving the hand of polyethylene terephthalate fabric by heat shrinking and hydrolyzing the fabric |
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3017685A (en) * | 1957-05-25 | 1962-01-23 | Heberlein Patent Corp | Process for the production of fabrics from specially prepared yarns |
US2995803A (en) * | 1959-05-21 | 1961-08-15 | Haveg Industries Inc | Process of preparing heat-resistant glass fabric |
US3111359A (en) * | 1959-10-16 | 1963-11-19 | Rohm & Haas | Modified textile and industrial fibers and fabrics and process for making them |
US3135577A (en) * | 1959-12-22 | 1964-06-02 | Ici Ltd | Process for improving the handle of polyethylene terephthalate fabrics with an alkali metal hydroxide and specific quaternary ammonium salts |
US3110617A (en) * | 1960-05-20 | 1963-11-12 | Du Pont | Textile |
US3287787A (en) * | 1960-09-30 | 1966-11-29 | Ici Ltd | Method of selectively weakening crimped polyester filaments and fibers |
US3096557A (en) * | 1961-01-03 | 1963-07-09 | Du Pont | Process for hot-wet calendering fabrics |
US3235426A (en) * | 1961-08-01 | 1966-02-15 | Du Pont | Method of rendering thermoplastic resins receptive to coatings |
US3245826A (en) * | 1963-06-12 | 1966-04-12 | Clevite Corp | Magnetic recording medium and method of manufacture |
US3302265A (en) * | 1964-04-21 | 1967-02-07 | Du Pont | Process for preparation of flannel fabrics from synthetic fibers |
US3731351A (en) * | 1970-10-12 | 1973-05-08 | Monsanto Co | Process of manufacturing tightly woven acrylic fabric |
US4008044A (en) * | 1975-06-03 | 1977-02-15 | J. P. Stevens & Co., Inc. | Treatment of polyester textiles to improve soil release and wettability properties |
US4270913A (en) * | 1979-07-06 | 1981-06-02 | Celanese Corporation | Pill-resistant polyester fabrics |
US5075990A (en) * | 1986-09-11 | 1991-12-31 | International Paper Company | Battery separator fabric method for manufacturing |
US4803256A (en) * | 1988-02-01 | 1989-02-07 | Dow Corning Corporation | Method of altering the surface of a solid synthetic polymer |
US4842792A (en) * | 1988-02-16 | 1989-06-27 | Eastman Kodak Company | Drafting process for preparing a modified polyester fiber |
US4996107A (en) * | 1988-02-16 | 1991-02-26 | Eastman Kodak Company | Ink reservoir containing modified polyester fibers |
WO1989007669A1 (en) * | 1988-02-16 | 1989-08-24 | Eastman Kodak Company | Modified grooved polyester fibers and process for production thereof |
US5124205A (en) * | 1988-02-16 | 1992-06-23 | Eastman Kodak Company | Ink reservoir containing modified polyester fibers |
US4872276A (en) * | 1988-05-13 | 1989-10-10 | Milliken Research Corporation | Calendering process for polyester fabric |
US5010663A (en) * | 1988-10-28 | 1991-04-30 | Stern & Stern Industries, Inc. | Low permeability fabric and method of making same |
EP0453678B1 (en) * | 1988-10-28 | 1995-01-11 | STERN & STERN INDUSTRIES, INC. | Low permeability fabric and method of making same |
WO2003080921A1 (en) * | 2002-03-25 | 2003-10-02 | Univerza V Ljubljani, Naravoslovnotehniska Fakulteta, Oddelek Za Tekstilstvo | PRETREATMENT METHOD OF POLyESTER FOR REDUCING ELIMINATION OF OLIGOMERS AT HIGH-TEMPERATURE ACID COLOURING WITH DISPERSION DYES |
US20150314326A1 (en) * | 2012-12-17 | 2015-11-05 | Kolon Glotech, Inc. | Method for manufacturing planarized fabric substrate for flexible display |
US10227725B2 (en) * | 2014-04-16 | 2019-03-12 | Cummins Filtration Ip, Inc. | Tuning surface properties of melt blown polyester fibers by hydrolysis and solution grafting |
US10760208B2 (en) | 2014-04-16 | 2020-09-01 | Cummins Filtration Ip, Inc | Tuning surface properties of melt blown polyester fibers by hydrolysis and solution grafting |
US20170370031A1 (en) * | 2014-12-25 | 2017-12-28 | Asahi Kasei Kabushiki Kaisha | Thin woven fabric having superior comfort |
US10961643B2 (en) * | 2014-12-25 | 2021-03-30 | Asahi Kasei Kabushiki Kaisha | Thin woven fabric having superior comfort |
Also Published As
Publication number | Publication date |
---|---|
GB847147A (en) | 1960-09-07 |
FR1192358A (en) | 1959-10-26 |
DE1140170B (en) | 1962-11-29 |
BE563152A (en) |
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