EP1356144A1 - Elastomere polyurethanfasern mit hoher effizienz bei der thermofixierung - Google Patents

Elastomere polyurethanfasern mit hoher effizienz bei der thermofixierung

Info

Publication number
EP1356144A1
EP1356144A1 EP01985172A EP01985172A EP1356144A1 EP 1356144 A1 EP1356144 A1 EP 1356144A1 EP 01985172 A EP01985172 A EP 01985172A EP 01985172 A EP01985172 A EP 01985172A EP 1356144 A1 EP1356144 A1 EP 1356144A1
Authority
EP
European Patent Office
Prior art keywords
poly
fiber
polymeric additive
solution
vinyl alcohol
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.)
Withdrawn
Application number
EP01985172A
Other languages
English (en)
French (fr)
Inventor
Hiroshi Nishikawa
Toshihiro Tanaka
Tomoharu Ima
Masahito Inoue
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Du Pont Toray Co Ltd
Original Assignee
Du Pont Toray Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Du Pont Toray Co Ltd filed Critical Du Pont Toray Co Ltd
Publication of EP1356144A1 publication Critical patent/EP1356144A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/94Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of other polycondensation products
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/70Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyurethanes

Definitions

  • the present invention relates to an elastomeric polyurethane fiber having selected polymeric additives therein. More particularly, the invention relates to such a fiber wherein the polymeric additives are poly(vinyl alcohol), modified poly(acrylic acid), or copolymers thereof.
  • non-elastomeric fibers are typically heat-set to provide the fabric or yarn with good dimensional stability, to shape and size the finished garment, and for other purposes such as ease of donning and doffing of high polyurethane fiber-content apparel.
  • Typical heat- setting temperatures used in commercial operations are 195°C for 6,6- nylon, I90°C for 6-nylon, and I80°C for cotton.
  • the relatively low temperatures suitable for fibers such as cotton put certain demands on the polyurethane fiber.
  • the polyurethane fiber has an acceptable heat-set efficiency only at temperatures used for the nylons, it cannot be heat-set in a fabric containing cotton, which will be damaged by exposure to such higher temperatures.
  • polyurethane fiber including incorporating polymeric additives such as a copolymer of diisopropylaminoethyl methacrylate and n-decyl methacrylate as disclosed in United States Patents US3428711 and a condensation polymer of p-cresol and divinyl benzene, as disclosed in United States Patent US3553290.
  • polymeric additives such as a copolymer of diisopropylaminoethyl methacrylate and n-decyl methacrylate as disclosed in United States Patents US3428711 and a condensation polymer of p-cresol and divinyl benzene, as disclosed in United States Patent US3553290.
  • the comfort of clothing may be improved under conditions of high humidity by increasing the moisture absorption-desorption characteristics of the fibers of which the clothing is comprised.
  • the tendency of certain fibers to cling to the body due to static electricity can be reduced by increasing the moisture absorption characteristics of the fibers.
  • Japanese Patent Application Publication JP2000144532 discloses a method of incorporating a polyethylene glycol-based polyurethane into polyurethane fiber.
  • Japanese Patent Application Publication JP09041204 discloses high moisture absorption-desorption biconstituent polyetheresteramide/polyamide fibers that can be combined with polyurethane fiber in downstream processing.
  • the elastomeric polyurethane fibers disclosed in the prior art do not simultaneously provide good heat-set efficiency and moisture absorption-desorption and whiteness retention, and an improved polyurethane fiber is still needed.
  • the present invention provides an elastomeric polyurethane fiber containing a polymeric additive having repeat units and selected from the group consisting of: poly(vinyl alcohol) and copolymers thereof, wherein at least about 1 mole % of the repeat units derived from vinyl acetate have hydroxyl groups, and at most about 99 mole % of the repeat units derived from vinyl acetate have hydroxyl groups; and modified poly(acrylic acid) and copolymers thereof, wherein acidic hydrogens in at least about 40 mole % of the repeat units derived from acrylic acid have been replaced with substantially non-acidic moieties; wherein the additive is present in the fiber at a level of at least about 0.5 wt% based on the weight of the fiber, and the additive is present in the fiber at a level of at most about 50 wt%, based on the weight of the fiber.
  • a polymeric additive having repeat units and selected from the group consisting of: poly(vinyl alcohol) and copolymers thereof, wherein at least about
  • the invention also provides a process for making such an elastomeric polyurethane fiber, comprising the steps of contacting a polymeric glycol with a diisocyanate to form a capped glycol, dissolving the capped glycol in a solvent, reacting the dissolved capped glycol with a chain extender to form the polyurethane in solution, adding the polymeric additive to the polyurethane solution, solution-spinning the polyurethane solution to form the fiber and collecting the fiber, particularly such a process wherein when the polymeric additive is poly(acrylic acid) or a copolymer thereof, and monoamine chain terminator is added to the polyurethane solution in an amount of at least about 40 mole % of the acid repeat units in the additive.
  • elastomeric polyurethane fiber and “polyurethane fiber” mean a staple fiber or continuous filament comprising polyurethane and which, free of diluents, has a break elongation in excess of 100% independent of any crimp and which when stretched to twice its length, held for one minute, and then released, retracts to less than 1.5 times its original length within one minute of being released. Spandex is an example of such a fiber.
  • Modified poly(acrylic acid) means a poly(acrylic acid) wherein in at least about 40 mole % of the repeat units, the acidic hydrogens have been replaced with a non-acidic moiety, for example a metal ion or an (alkyl)ammonium ion.
  • the elastomeric polyurethane fiber of the invention contains a polymeric additive selected from the group consisting of poly(vinyl alcohol), modified poly(acrylic acid), and copolymers thereof.
  • the polymeric additive has a selected range of solution viscosities and number average molecular weights.
  • the polymeric additive is poly(vinyl alcohol) or a copolymer thereof, it can have a number average molecular weight in the range of at least about 1 ,000 and at most about 1 ,000,000, as determined by gel permeation chromatography using a polystyrene standard.
  • the polymeric additive when the polymeric additive is a modified poly(acrylic acid) or a copolymer thereof, its number average molecular weight can be at least about 1 ,000 and at most about 20,000,000, as determined by the same method.
  • Any of the classes of polymeric additives contained in the polyurethane fiber of the invention and used in the process of the invention can have a Brookfield viscosity at 20°C in the range of at least about 200 centiPoise and at most about 10,000 Poise as a 5 wt% solution in DMAc, based on the weight of the solution.
  • the solution viscosity of the polymeric additive typically rises as the number average molecular weight rises.
  • the content of the polymeric additive in the elastomeric polyurethane fiber is at least about 0.5 wt% and at most about 50 wt%, preferably least about 1 wt% and at most about 30 wt% based on the weight of the polyurethane fiber, for good spinnability, heat set, whiteness retention, and moisture absorption-desorption.
  • a higher weight percent of the additive can be present in the fiber and used in the process of the invention.
  • the polymeric additive is poly(vinyl alcohol) ("PVA") or a copolymer thereof
  • PVA poly(vinyl alcohol)
  • it can be prepared by hydrolyzing to hydroxyl groups some of the acetyl groups in poly(vinyl acetate) or a copolymer thereof. After such hydrolysis, at least about 1 mole percent and at most about 99 mole percent, preferably at least about 10 mole percent and at most about 90 mole percent of the repeat units derived from vinyl acetate have hydroxyl groups.
  • the poly(vinyl alcohol) copolymer can comprise repeat units derived from ethylene, alkyl methacrylate(s), vinyl sulfonate, vinyl acetate, styrene sulfonic acid, and the like.
  • Such a polymeric additive can be for example poly(vinyl alcohol-co-vinyl acetate-co-vinyl sulfonate), poly(vinyl alcohol-co-vinyl acetate), poly(vinyl alcohol-co-vinyl phosphate), poly(vinyl alcohol-co-vinyl acetate-co-ethylene), and poly(vinyl alcohol-co- vinyl acetate-co-alkyl methacrylate) wherein the alkyl moiety has one to three carbons.
  • Poly(vinyl alcohol-co-vinyl acetate-co-vinyl sulfonate) is preferred.
  • At least about 50 mole % of the repeat units can be derived from acrylic acid and can have the following general formula:
  • OX wherein X is acidic hydrogen in less than 60 mole percent of the repeat units, the acidic hydrogens in at least about 40 mole percent of the the repeat units derived from acrylic acid having been replaced with substantially non-acidic moieties, for example alkali metal ion, ammonium, alkylammonium, dialkylammonium, and alkyl moieties wherein the alkyls have 1 to 3 carbon atoms.
  • substantially non-acidic moieties for example alkali metal ion, ammonium, alkylammonium, dialkylammonium, and alkyl moieties wherein the alkyls have 1 to 3 carbon atoms.
  • Comonomers in such polymeric additives can include maleic acid, acrylamide, N,N-dialkylacrylamide, styrene sulfonic acid, ethylene sulfonic acid, methacrylic acid, sodium maleate, sodium styrene sulfonate, methacrylate esters, ethylene, dimethylaminoethyl acrylate, dimethylaminoethyl methacrylate, dialkylammonium acrylate (for example diethylammonium acrylate generated by addition of excess diethylamine chain terminator to the polyurethane spinning solution followed by addition of poly(acrylic acid)), dimethylammonium diallyl chloride and the like.
  • modified poly(acrylic acid) additives examples include poly(dialkylammonium acrylate), poly(sodium acrylate), poly(methyl acrylate), poly(potassium acrylate), poly(dialkylammonium acrylate), poly(sodium acrylate-co-acrylamide), poly(sodium acrylate-co- sodium styrene sulfonate), poly(ammonium acrylate), poly(alkylammonium acrylate-co-N-alkylacrylamide), poly(acrylic acid-co-sodium acrylate-co- acrylamide), and the like.
  • Elastomeric polyurethane fiber can be prepared by contacting a polymeric glycol (for example a polyether glycol, a polyester glycol, or a polycarbonate glycol) with a diisocyanate and a difunctional chain extender and spinning the resulting polyurethane.
  • a polymeric glycol for example a polyether glycol, a polyester glycol, or a polycarbonate glycol
  • Useful polyether glycols include, for example, poly(tetramethyleneether glycol, poly(1 ,2-propyleneether) glycol, poly(tetramethyleneether-co-3-methyl-tetramethyleneether) glycol, and poly(tetramethyleneether-co-2,3-dimethyl-tetramethyleneether) glycol, and the like.
  • Useful polyester glycols include poly- ⁇ -caprolactone diol and hydroxy-terminated reaction products of diols such as ethylene glycol, 1 ,3- propane diol, 1 ,4-butane diol, 1 ,6-hexane diol, 2,2-dimethyl-1 ,3-propane diol, 3-methyl-1 ,5-pentane diol, and mixtures thereof with dicarboxylic acids such as adipic acid, 1 ,9-nonanedioic acid, and 1 ,12-dodecanedioic acid, and the like.
  • diols such as ethylene glycol, 1 ,3- propane diol, 1 ,4-butane diol, 1 ,6-hexane diol, 2,2-dimethyl-1 ,3-propane diol, 3-methyl-1 ,5-pentane diol, and mixtures thereof with dicarboxylic acids such as
  • Useful polycarbonate glycols include poly(pentane-1 ,5- carbonate) diol, poly(hexane-1 ,6-carbonate) diol, and the like. Such glycols can have a number-average molecular weight of at least 1 ,000 and at most 8,000, preferably at least 1 ,800 and at most 6,000.
  • Useful diisocyanates include 4-methyl-1 ,3-phenylene diisocyanate, 1-isocyanato-4-[(4-isocyanatophenyl)methyl]benzene, mixtures of 1- isocyanato-4-[(4-isocyanatophenyl)methyl]benzene and 1 -isocyanato-2- [(4-isocyanatophenyl)methyl]benzene, 1 ,4-diisocyanatobenzene, 1 ,3- diisocyanatoxylylene, 1 ,4-diisocyanatoxylylene, 2,6-napthalene diisocyanate, 5-isocyanato-1-(isocyanatomethyl)-1 ,3,3- trimethylcyclohexane, 1 ,1'-methylenebis(4-isocyanatocyclohexane), 2,4- diisocyanato-1-methylcyclohexane, 2,6-diisocyanato-1
  • Useful diamine chain extenders include ethylene diamine, 1 ,2- propane diamine, 1 ,3-propane diamine, 1 ,6-hexamethylene diamine, 1 ,3- xylylenediamine, p-phenylene diamine, p-xylylene diamine, m-xylylene diamine, p.p'-methylene dianiline, bis(4-aminophenyl)phosphine oxide, N- methylbis(3-aminopropyl)amine, 1 ,4-cyclohexanediamine, 1 ,3- cyclohexanediamine, 2-methyl-1 ,5-pentanediamine, 1 ,3-pentanediamine, mixtures thereof, and the like.
  • Useful diol chain extenders include ethylene glycol, 1 ,3-propane diol, 1 ,2-propane diol, 2,2-dimethyl-1 ,3- propane diol, 1,4-butane diol, 3-methyl-1 ,5-pentane diol, 1 ,6-hexane diol, bis(2-hydroxyethylene terephthalate), 1 ,4-bis( ⁇ -hydroxyethoxy)benzene, N-methylbis(2-hydroxypropyl)amine, mixtures thereof, and the like.
  • diol-extended polyurethanes When diol-extended polyurethanes are to be made, it can be advantageous to use one or more polymerization catalysts.
  • Typical amine catalysts include, for example, N,N-dimethylcyclohexylamine, N,N- dimethylbenzylamine, triethylamine, N-methylmorpholine, N- ethylmorpholine, N,N,N',N'-tetramethylethylene diamine, N,N,N',N'- tetramethyl-1 ,3-propane diamine, N,N,N',N'-tetramethylhexane diamine, bis-2-dimethylamino ethyl ether, N,N,N',N',N"-pentamethyldiethylene triamine, tetramethyl guanidine, triethylene diamine, N.N'-dimethyl piperazine, N-methyl-N'-dimethylamino ethyl-piperazine, N-(2- dimethylamino ethyl) morpholine, 1 -methyl imidazole, 1 ,2-dimethyl imi
  • a small amount of a monofunctional chain terminator can be used, for example diethylamine, diisopropyl amine, ethylmethyl amine, diethyl amine, methylpropyl amine, isopropylmethyl amine, diisopropyl amine, butylmethyl amine, isobutylmethyl amine, isopentylmethyl amine, dibutyl amine, diamyl amine, ethanol, propanol, butanol, hexanol, n-pentylamine, n-hexylamine, cyclohexylamine, n-heptylamine, methylcyclohexylamines (for example 1-amino-3-methylcylohexane, 1-amino-2-methylcyclohexane, and 1-amino-3,3,5-trimethylcyclohexane), n-dodec
  • the polyurethane of which the elastomeric polyurethane fiber of the invention is comprised and which is prepared and spun in the process of the invention can have a number average molecular weight of at least 40,000 and at most 150,000, as measured by gel permeation chromatographic analysis using a polystyrene standard.
  • the elastomeric polyurethane fiber of the invention can have a 'high-side' melting point of at least 200°C and at most 260°C, as determined by 'second pass' differential scanning calorimetry.
  • the polyurethane fiber can contain additional stabilizers, pigments and the like, provided such additives to not detract from the benefits of the invention.
  • additives include benzotriazole-based stabilizers, ultraviolet light absorbers, other light resistance agents, antioxidants, anti- tack agents, lubricants such as mineral oil and silicone oils, antistatic agents and the like.
  • additives include hindered phenolic stabilizers such as 2,6-di-f-butyl-4-methylphenol, hindered amine stabilizers, inorganic pigments such as titanium oxide, zinc oxide, carbon black and the like, metal salts such as magnesium stearate and barium sulfate, hydrotalcite, mixtures of huntite and hydromagnesite, bactericides containing silver, zinc, or compounds thereof, deodorants, a variety of anti-static agents, phosphoric acids, and so on.
  • hindered phenolic stabilizers such as 2,6-di-f-butyl-4-methylphenol
  • hindered amine stabilizers inorganic pigments such as titanium oxide, zinc oxide, carbon black and the like
  • metal salts such as magnesium stearate and barium sulfate, hydrotalcite, mixtures of huntite and hydromagnesite, bactericides containing silver, zinc, or compounds thereof, deodorants, a variety of anti-static agents, phosphoric acids,
  • melt-spinning or wet-spinning (herein collectively 'solution spinning') or melt-spinning can be used to make the polyurethane fiber.
  • melt-polymerization or solution polymerization can be used, and the polymerization can be carried out in one step or two steps.
  • the process of the invention comprises a solution-spinning . step (which is preferred), a two-step solution polymerization process can be used.
  • the polymeric glycol is first contacted with the diisocyanate to form a "capped glycol", which is a mixture of isocyanate- terminated glycol and unreacted diisocyanate.
  • the mole ratio ("capping ratio") of diisocyanate to glycol can be about 1.5 to 4.5.
  • the capped glycol is then dissolved in a solvent, for example dimethylacetamide (“DMAc”), dimethylformamide, dimethylsulfoxide, N-methyl-pyrrolidone, or the like.
  • At least one chain extender and optionally a small amount of chain terminator are reacted with the capped glycol in solution to form a polyurethane(urea) solution.
  • a one-step solution polymerization process can also be used, in which the polymeric glycol, diisocyanate, and at least one diol chain extender are contacted with each other in the solvent substantially simultaneously.
  • the polymeric stabilizer selected from the group consisting of poly(vinyl alcohol), modified poly(acrylic acid), and copolymers thereof is then added.
  • any suitable apparatus can be used to mix the polymeric additive into the polyurethane solution, for example a static mixer, an agitator, a homogenizer, or a twin screw extruder; the additive can be added as a solution or a dispersion for greater uniformity of mixing.
  • the effect of adding the polymeric additive to the polyurethane solution can be tested on a small scale.
  • addition of a (co)poly(acrylic acid) can increase the solution viscosity more than expected or desired, in which case excess chain terminator can be added to the polyurethane solution before adding the (co)poly(acrylic acid).
  • the amount of chain terminator added, and the amount of acidic hydrogens replaced on the acrylic acid-derived repeat units can be at least about 40 mole%, based on the moles of repeat units derived from acrylic acid in the (co)poly(acrylic acid). For example, adding excess diethylamine chain extender to the polyurethane solution before adding poly(acrylic acid) avoids excessive increases in solution viscosity.
  • poly(acrylic acid) is modified and that poly(diethylammonium acrylate-co-acrylic acid) is formed. It is also believed that some repeat units formally derived from N,N- diethylacrylamide are generated.
  • the resulting spinning solution optionally containing other additives, can then be spun through a spinneret into a heated column in which the solvent evaporates from the polymer to form the polyurethane fiber.
  • the fiber After leaving the heated column, the fiber is collected, for example by passing it around a feed (“Godet”) roll and then winding it up at a speed of at least 450 m/min and at a feed roll:winder speed ratio of at least 1 :1.15 and at most 1 :1.65, preferably at most 1 :1.40 and more preferably at most 1 :1.35.
  • a feed "Godet" roll and then winding it up at a speed of at least 450 m/min and at a feed roll:winder speed ratio of at least 1 :1.15 and at most 1 :1.65, preferably at most 1 :1.40 and more preferably at most 1 :1.35.
  • Instron 4502 tensile tester A 5 cm (length L1) fiber sample was subjected to 5 stretch-and-relax cycles to 300% elongation at a speed of 50 cm/min. On the fifth stretch cycle the stress (G1) was measured at 300% elongation, the sample was held at 300% elongation for 30 seconds, and the stress (G2) was again measured. Then the sample was allowed to relax until it reached a stress of 0, at which point its length (L2) was again measured. On a sixth cycle, the sample was extended until it broke, and the stress (G3) at the break and the sample length (L3) at the break were measured.
  • the sample's properties were calculated according to the following equations:
  • Heat Set Efficiency, % 100 x (L6 - L5)/L5
  • a moisture absorption-desorption coefficient, ⁇ MR was determined on knit tube samples weighing about 1 gram each which had been equilibrated for 24 hours under various conditions in a constant temperature, constant relative humidity (“RH") oven (Tabai Co. oven model PR-2G). Each sample was thoroughly dried at 105°C for 2 hours in a hot-air oven and cooled for 30 minutes in a desiccator to establish its 'absolute dry weight', and then it was exposed to conditions of higher temperature and humidity.
  • the moisture absorption-desorption coefficient was calculated from the following equation:
  • MR2 100 x (W30 X 90 - ADW)/ADW
  • MR1 100 x (W 2 rj ⁇ 65 - ADW)/ADW
  • W30 ⁇ 90 is the weight of the sample after 24 hours' equilibration at 30°C and 90%RH
  • W20x65 is the weight of the sample after 24 hours' equilibration at 20°C and 65%RH
  • ADW is the absolute dry weight.
  • the coefficient ⁇ MR represents the difference in moisture absorption between in-clothing conditions (30°C and 90%RH, similar to participation in light to medium effort) and outdoor conditions (20°C and 65%RH) and indicates the release of moisture from the clothing to the outside atmosphere.
  • UV light carbon arc
  • Sunshine Weather Meter Wel-Sun-HCH Model B, sold by Suga Shikenki K.K., Shinjuku-Ku, Tokyo, Japan.
  • similarly prepared samples were exposed for 20 hours to 10ppm NO2 gas in air in a Scott Controlled Atmosphere tester (made by Scott Research Laboratories, Inc.) at 40°C and 60% RH.
  • a calibration curve was first prepared from a first sample of the fiber to be analyzed.
  • the first 1g sample of the fiber containing the polymeric additive was washed with n-hexane and completely dissolved in 50ml of DMAc. Ethanol (100 ml) was very slowly added to precipitate the polymeric additive, the precipitate was filtered off and dissolved and re-precipitated, and the remaining polyurethane solution was filtered and evaporated to dryness to isolate the polyurethane from the first fiber sample.
  • the polyurethane and polymeric additive were re-mixed in known weight ratios of 0wt%, 1wt%, 3wt%, 6wt%, 10wt%, 20wt%, and 40wt% additive, based on total polymer weight.
  • the mixtures were re-dissolved in DMAc, the resulting solutions were cast into films, and IR spectra of the films were taken with an AFT-IR instrument (Perkin Elmer Company).
  • a second 1g sample of the fiber to be analyzed was washed with n-hexane, dissolved in DMAc, and cast into a film without separating the polyurethane from the additive, and its IR spectrum was measured.
  • a similar IR peak area ratio (X s ) was obtained between the v(CO) bands and the v(OH) peak for (co)poly(vinyl alcohol) or the v (CO) band for (co)poly(acrylic acid).
  • the additive content was calculated according to the following formula:
  • a dispersion of poly(vinyl alcohol) (Gohsenol®, Nippon Gohsei Kagaku KK; number average molecular weight 500,000, degree of saponification 88, viscosity 2,200 Poise) was prepared in DMAc using a horizontal Wiley mill (A. Bachofen Company, DYNO-MIL JDL) filled with 85% zirconia beads at a flow rate of 50g/min.
  • the PVA dispersion was 35 wt% based on total dispersion weight and was labelled B1.
  • a stabilizer additive mixture labelled C1 was prepared from a 2:1 weight ratio of Methacrol® 2462B ((bis(4- isocyanatocyclohexyl)methane) and N-t-butyldiethanolamine) and
  • Methacrol® 2390 D (condensation polymer of p-cresol and divinyl benzene) (both registered trademarks of E. I. du Pont de Nemours and Company) in DMAc at a level of 35wt% additives, based on total mixture weight.
  • Solution A1 , dispersion B1 , and mixture C1 were uniformly mixed in amounts such that the final polyurethane fiber had 5 wt% PVA and 2 wt% of the stabilizer additives, based on total fiber weight.
  • the resulting spinning solution, D1 was dry-spun at a speed ratio of 1.4 between the Godet (feed) roll and the windup and wound up at 540 m/min to obtain 200 g of a 20 decitex monofilament elastomeric polyurethane fiber.
  • the polyurethane fiber was single-covered with "Miracosmo" (22 decitex nylon yarn, manufactured by Toray KK), and the covered polyurethane fiber was used to knit pantyhose in which the covered fiber was present in every course; the pantyhose had excellent visual and tactile aesthetics. Its moisture absorption-desorption coefficient is presented in Table 1.
  • a 35 wt% dispersion of poly(vinyl alcohol) (SMR resin ®, Shin-Etsu Kagaku KK; number average molecular weight 100,000; viscosity 200 Poise) was prepared in DMAc by the same method as in Example 1 and labelled B2.
  • Solution A1 , dispersion B2, and mixture C1 were uniformly mixed to obtain a spinning solution D2 at ratios such that in the final elastomeric polyurethane fiber the PVA was present at a level of 20 wt% and the stabilizer additives were present at a total level of 2 wt%, based on fiber weight.
  • Solution D2 was dry spun at a speed ratio of 1.40 between the Godet roll and windup and wound up at 540 m/min to obtain 200 g of a 20 decitex, monofilament polyurethane fiber.
  • the polyurethane fiber was covered and knit as in Example 1 , and the resulting pantyhose had excellent visual and tactile aesthetics.
  • Table 1 presents physical properties of the polyurethane fiber and the moisture absorption- desorption coefficient of the pantyhose.
  • a dispersion of a sulfonic acid-modified poly(vinyl alcohol), believed to be poly(sodium allyl sulfonate-co-vinyl alcohol), (Gohseran®, Nippon Gosei Kagaku KK; number average molecular weight 20,000, degree of saponification 45, viscosity 110 Poise) in DMAc was prepared as described in Example 1 and labelled B3.
  • Solution A2, dispersion B3, and mixture C1 were uniformly mixed to give a spinning solution D3 in a ratio such that the final elastomeric polyurethane fiber contained 30 wt% PVA and 2 wt% stabilizer additive mixture, based on fiber weight.
  • Example 4 The solution D3 was dry spun at a speed ratio of 1.20 between the Godet roll and windup and wound up at 600 m/min to give 500 g of 20 decitex multifilament polyurethane fiber.
  • the polyurethane fiber was covered and knit as described in Example 1 to make an every-course pantyhose having excellent visual and tactile aesthetics. Polyurethane fiber and pantyhose properties are presented in Table 1.
  • Polyftetramethylene ether) glycol of number-average molecular weight 1800 (687 g) and 1 -isocyanato-4-[(4- isocyanatophenyl)methyl]benzene (166 g) (diisocyanate:glycol mole ratio 1.74:1) were contacted with each other to make a capped glycol which was dissolved in 1625 g DMAc, chain-extended with 15.12 g ethylene diamine and 3.78 g 1 ,3-cyclohexanediamine (80/20 molar ratio), and chain-terminated with 2.68 g diethylamine to make polyurethane solution A3, which was 35 wt% polyurethane, based on total solution weight.
  • Solution A3, dispersion B3, and mixture C1 were uniformly mixed to obtain spinning solution D4 at ratios such that the final elastomeric polyurethane fiber contained 35 wt% PVA and 2 wt% stabilizer additives, based on fiber weight.
  • Solution D4 was dry spun using a speed ratio of 1.30 between the Godet roll and the windup and was wound up at 600 m/min to obtain 500 g of 20 decitex multifilament polyurethane fiber having a poly(vinyl alcohol) content of 35 wt%, based on total fiber weight.
  • the polyurethane fiber was covered and knit as in Example 1 to give pantyhose with excellent visual and tactile aesthetics. Polyurethane fiber and pantyhose properties are given in Table 1.
  • Example 1 was repeated but without adding dispersion B1.
  • the dry-spun monofilament elastomeric polyurethane fiber had a linear density of 18 decitex. It was covered and knit as in Example 1. Its properties and those of the pantyhose are given in Table 1.
  • Example 3 was repeated but without dispersion B3.
  • the resulting 20 decitex multifilament elastomeric polyurethane fiber was covered and knit as in Example 1. Its properties and those of the pantyhose are given in Table 1.
  • Table 1 shows that the elastomeric polyurethane fiber of the invention displays improved heat-set efficiencies and much higher moisture absorption-desorption coefficients while still retaining good elongation, tensile, set, and stress relaxation properties. Further, its whiteness retention after exposure to UV, NO2, or chlorine is substantially improved over polyurethane fiber not of the invention.
  • Example 1 was repeated, except that a 35 wt% dispersion of a poly(sodium acrylate-co-acrylamide) (Sanfloc ®, a product of Sanyo Kasei Co.; sodium acrylate:acrylamide mole ratio 90:10, number average molecular weight 5,000,000, viscosity 8,000 Poise) was prepared in DMAc and labelled B4.
  • Solution A1 , dispersion B4, and mixture C1 were uniformly mixed to obtain spinning solution D5 and in amounts such that the final elastomeric polyurethane fiber had 5 wt% poly(sodium acrylate- co-acrylamide) and 2 wt% of the stabilizer additives, based on total fiber weight.
  • Solution D5 was then dry-spun as in Example 1 to form the polyurethane fiber, whose properties are summarized in Table 1.
  • the elastomeric polyurethane fiber was single-covered and knit as in Example 1 to give a pantyhose with excellent visual and tactile aesthetics. Its moisture absorption-desorption coefficient is also presented in Table 1.
  • a 35 wt% dispersion of a copolymer of sodium acrylate-sulfonic acid (Aqualic®; number average molecular weight 60,000, viscosity 200 Poise; a product of Nippon Shokubai (Catalyst) KK) was prepared in DMAc by the same method as in Example 1 and labelled B5.
  • Solution A1 , dispersion B5, and mixture C1 were uniformly mixed to obtain a solution D6 and in relative amounts such that in the final elastomeric polyurethane fiber the sodium acrylate-sulfonic acid additive was 20 wt% and the stabilizer additives were 2 wt%, based on weight of fiber.
  • Solution D6 was dry-spun as in Example 1 to give the polyurethane fiber, whose properties are summarized in Table 2.
  • the elastomeric polyurethane fiber was single-covered and knit as in Example 1 to give a pantyhose with excellent visual and tactile aesthetics. Its moisture absorption-desorption coefficient is presented in Table 1.
  • Example 7 Example 3 was repeated except that a fine dispersion of poly(sodium acrylate) (Aqualic®; number average molecular weight 3,500, viscosity 150 Poise; a product of Nippon Shokubai (Catalyst) KK) was prepared in DMAc using the method described in Example 1 and labelled B6.
  • Solution A2, dispersion B6, and mixture C1 were uniformly mixed to give a spinning solution D7 and in amounts such that the final fiber had 25 wt% poly(sodium acrylate) and 2 wt% stabilizer additives, based on total weight of fiber.
  • Solution D7 was then dry-spun as described in Example 3 to give the elastomeric polyurethane fiber, whose properties are presented in Table 2.
  • the polyurethane fiber was covered and knit as described in Example 1 to give pantyhose with excellent appearance and tactile aesthetics and whose moisture absorption-desorption coefficient ⁇ MR is also given in Table 2.
  • Example 8 Example 4 was repeated, except that dispersion B6 was used in an amount such that 30 wt% of poly(sodium acrylate) was present in the final polyurethane fiber, based on weight of fiber, to give a spinning solution D8 which was then dry-spun as described in Example 7 to give the polyurethane fiber, whose properties are also given in Table 2.
  • the elastomeric polyurethane fiber was covered and knit as described in Example 1 to give a pantyhose whose visual and tactile aesthetics were excellent and whose moisture absorption-desorption coefficient ⁇ MR is presented in Table 2. Comparative Example 4
  • Example 5 was repeated but without adding dispersion B4.
  • the dry-spun monofilament elastomeric polyurethane fiber had a linear density of 18 decitex. It was covered and knit as in Example 1 , and its properties and those of the pantyhose made from it are given in Table 2.
  • Example 7 was repeated but without adding dispersion B6.
  • the properties of the resulting elastomeric polyurethane fiber and of pantyhose knit from the covered polyurethane fiber are given in Table 2.
  • Example 8 was repeated but without adding dispersion B6.
  • the properties of the resulting elastomeric polyurethane fiber and of pantyhose knit from the covered polyurethane fiber are given in Table 2.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP01985172A 2000-12-20 2001-12-20 Elastomere polyurethanfasern mit hoher effizienz bei der thermofixierung Withdrawn EP1356144A1 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2000386745 2000-12-20
JP2000386746 2000-12-20
JP2000386746 2000-12-20
JP2000386745 2000-12-20
PCT/US2001/050772 WO2002050349A1 (en) 2000-12-20 2001-12-20 Elastomeric polyurethane fiber with high heat-set efficiency

Publications (1)

Publication Number Publication Date
EP1356144A1 true EP1356144A1 (de) 2003-10-29

Family

ID=26606163

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01985172A Withdrawn EP1356144A1 (de) 2000-12-20 2001-12-20 Elastomere polyurethanfasern mit hoher effizienz bei der thermofixierung

Country Status (3)

Country Link
EP (1) EP1356144A1 (de)
KR (1) KR20030070072A (de)
WO (1) WO2002050349A1 (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100461760B1 (ko) * 2002-11-29 2004-12-14 주식회사 효성 폴리우레탄 탄성사의 제조 방법
KR100851740B1 (ko) * 2004-12-30 2008-08-11 주식회사 효성 세트성 및 염색 견뢰도가 우수한 폴리우레탄 탄성사 및 그제조 방법
EP2829642A4 (de) * 2011-12-16 2015-12-16 Toray Opelontex Co Ltd Elastische polyurethanfaser und verfahren zur herstellung davon

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1084657A (en) * 1963-10-23 1967-09-27 Kurashiki Rayon Kk Polyurethane composition having superior light resistance and mechanical properties
US4895902A (en) * 1988-07-28 1990-01-23 E. I. Dupont De Nemours And Company Hindered tertiary amine aminoalkyl methacrylate stabilizer for spandex
US5362432A (en) * 1993-04-02 1994-11-08 E. I. Du Pont De Nemours And Company Process for dry spinning spandex
TW589421B (en) * 2000-04-26 2004-06-01 Du Pont Spandex with high heat-set efficiency

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0250349A1 *

Also Published As

Publication number Publication date
KR20030070072A (ko) 2003-08-27
WO2002050349A1 (en) 2002-06-27

Similar Documents

Publication Publication Date Title
JP3717186B2 (ja) ポリウレタン弾性繊維及びその製造方法
JP6133254B2 (ja) 2成分スパンデックス
JP5168401B2 (ja) ポリウレタン弾性糸およびその製造方法
JP5704530B2 (ja) ポリウレタン弾性糸およびその製造方法
US6639041B2 (en) Spandex having low set at low temperatures
US20040019146A1 (en) Elastomeric polyurethane fiber with high heat-set efficiency
JP5659781B2 (ja) ポリウレタン弾性糸およびその製造方法
WO2002050349A1 (en) Elastomeric polyurethane fiber with high heat-set efficiency
JP3826378B2 (ja) ポリウレタン糸およびその製造方法
KR100555269B1 (ko) 폴리(비닐리덴 플루오라이드) 함유 폴리우레탄 섬유
US6376071B1 (en) Polyurethane fiber containing poly(vinylidene fluoride)
JP2963856B2 (ja) アミノ変性シリコーンを含有するポリウレタン弾性繊維
JP3826377B2 (ja) ポリウレタン糸およびその製造方法
JPH10310934A (ja) 弾性糸およびその製法ならびにポリウレタンウレア溶液
EP1311578B1 (de) Spandex mit niedriger bleibender verformung bei niedrigen temperaturen
JP5141975B2 (ja) ポリウレタン弾性糸およびその製造方法
EP1025294B1 (de) Verfahren zur herstellung von spandexfasern und daraus hergestellte spandexfasern
JP4013178B2 (ja) スパンデックス糸の製造方法
JP2006144192A (ja) ソフトストレッチ性ポリウレタン弾性糸およびその製造方法
WO1998025986A1 (en) Polyestercarbonate-polyurethaneurea fibers
JP2002363823A (ja) 吸湿性ポリウレタン弾性繊維およびその製造方法
JP6075036B2 (ja) ポリウレタン弾性糸およびその製造方法
JP2000178859A (ja) 編 地

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20030522

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

RBV Designated contracting states (corrected)

Designated state(s): AT BE CH DE FR IT LI

17Q First examination report despatched

Effective date: 20041111

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RBV Designated contracting states (corrected)

Designated state(s): DE FR IT

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20060112