WO2005068695A1 - Process for preparing poly(trimethylene terephthalate) fiber - Google Patents

Process for preparing poly(trimethylene terephthalate) fiber Download PDF

Info

Publication number
WO2005068695A1
WO2005068695A1 PCT/US2005/000774 US2005000774W WO2005068695A1 WO 2005068695 A1 WO2005068695 A1 WO 2005068695A1 US 2005000774 W US2005000774 W US 2005000774W WO 2005068695 A1 WO2005068695 A1 WO 2005068695A1
Authority
WO
WIPO (PCT)
Prior art keywords
filaments
yarn
drawn
speed
denier
Prior art date
Application number
PCT/US2005/000774
Other languages
English (en)
French (fr)
Inventor
Jing-Chung Chang
Richard L. Dommel
Original Assignee
E.I. Dupont De Nemours And Company
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 E.I. Dupont De Nemours And Company filed Critical E.I. Dupont De Nemours And Company
Priority to EP05711340A priority Critical patent/EP1702092A4/en
Priority to MXPA06007683A priority patent/MXPA06007683A/es
Priority to CA002552662A priority patent/CA2552662A1/en
Priority to JP2006549507A priority patent/JP2007521422A/ja
Priority to CN200580001824XA priority patent/CN1906340B/zh
Publication of WO2005068695A1 publication Critical patent/WO2005068695A1/en

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
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/62Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G1/00Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
    • D02G1/02Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics by twisting, fixing the twist and backtwisting, i.e. by imparting false twist
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G1/00Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
    • D02G1/20Combinations of two or more of the above-mentioned operations or devices; After-treatments for fixing crimp or curl
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02JFINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
    • D02J1/00Modifying the structure or properties resulting from a particular structure; Modifying, retaining, or restoring the physical form or cross-sectional shape, e.g. by use of dies or squeeze rollers
    • D02J1/08Interlacing constituent filaments without breakage thereof, e.g. by use of turbulent air streams
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/04Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2503/00Domestic or personal
    • D10B2503/04Floor or wall coverings; Carpets

Definitions

  • Polyesters prepared by condensation polymerization of the reaction product of a diol with a dicarboxylic acid can be spun into yarn.
  • U.S. Pat. No. 3,998,042 describes a process for preparing poly(ethylene terephthalate) yarn in which the extruded fiber is drawn at high temperature (160° C.) with a steam jet assist, or at a lower temperature (95° C.) with a hot water assist.
  • Poly(ethylene terephthalate) can be spun into bulk continuous filament (BCF) yarn in a two-stage drawing process in which the first stage draw is at a significantly higher draw ratio than the second stage draw.
  • BCF bulk continuous filament
  • U.S. Pat. No. 6,284,370 relates to a poly(trimethylene terephthalate) fiber which has a suitable thermal stress and a suitable boil- off shrinkage and which gives a fabric, when woven or knitted, showing less stiffness caused by excessive shrinkage, and manifesting softness and the excellent color developing property expected from the low elastic modulus characteristic of the fiber.
  • the intrinsic viscosity of a polymer used in the invention is preferably from 0.4 to 1.5, more preferably from 0.7 to 1.2.
  • the polyester fiber of the invention preferably is in the form of multifilament yarn when used for clothing applications. Although the total size of the yarn is not restricted, it is usually from 5 to 200 d (denier), preferably from 20 to 150 d.
  • the poly(trimethylene terephthalate) has an intrinsic viscosity of about 0.95 to about 1.10.
  • a process comprises: (a) extruding molten poly(trimethylene terephthalate) polymer having an intrinsic viscosity in the range of about 0.95 to about 1.10, a water content of less than about 100 ppm, a number average molecular weight of about 26500 to about 50000 and a melt viscosity of about 350 to about 1000 Pascals at 250°C and 48.65 per second shear rate through a spinneret to form filaments; (b) converging the filaments into yarn; (c) cooling the extruded filaments; (d) coating the cooled filaments with a spin finish; optionally pre-intermingling the filaments; (e) optionally heating the coated filaments to a temperature greater than the glass transition temperature of the polymer filaments, but less than about 200°C; (f) drawing the optionally heated filaments at a speed of greater than 3000 meters per minute to produce filaments having a filament denier greater than 1 and yarn having a yarn denier greater than 210
  • the melt viscosity of the polymer is at least about 350, more preferably at least about 400, even more preferably at least about 450 and most preferably at least about 500 Pascals at 250°C and 48.65 per second shear rate.
  • the melt viscosity is up to about 1000, more preferably up to about 900, even more preferably up to about 800 and most preferably up to about 700 Pascals at 250°C and 48.65 per second shear rate. Drying is preferably carried out at about 80° C. or higher and about 180° C. or lower, most preferably at about 150° C.
  • Polymer holdup time in transfer pipe 22 should be kept at a minimum, for example, below 20 minutes, preferably below 10 minutes, most preferably below 2 minutes. This can be accomplished, for example, by reducing the length and/or diameter of the piping and/or increasing throughput by using a booster pump.
  • the metering pump 24 meters the polymer composition to the spinneret or die 26.
  • the polymer is extruded through the spinneret or die 26 to form filaments 2.
  • Spun filaments are cooled in cooling zone 3 by a radial flow or cross flow of gas to below the polymer glass transition temperature.
  • a spin finish or oil can be applied to the solidified filaments by finish applicator 4. Following the finish application and prior to the meter roll the filaments can be treated with turbulent air in the optional preintermingling device 5 to even out the finish on the filaments.
  • the spin pack metering pump and spinneret or die may be heated through conventional means (e.g., Dow fluid or hot oil).
  • the throughput is a function of the number of spin positions and typically is anywhere from about 2 pounds/hour (about 0.9 kg/hour) to commercial scales of about 2,000 pounds/hour (about 907 kg/hour) to about 3,000 pounds/hour (about 1 ,361 kg/hour) per spinning machine (i.e., per one remelter) or higher.
  • the cooling zone 3 cools the filaments by a radial flow or cross flow of gas, typically humidified air at a temperature preferably of about 10° C. or above and preferably about 30° C. or below applied at about 0.2 m/sec or more and about 0.8 m/sec or less.
  • the filaments are converged into yarn at roller 6.
  • the filaments are then drawn by use of a supplying roller 6 and a set of drawing rollers 7.
  • the filaments are preferably drawn at a draw ratio of about 1.1 to about 4.0.
  • the draw ratio can be about 1.2 to about 3.0 or even 1.4 to 2.2.
  • the filaments can then be crimped through a bulking unit 8 with a texturing nozzle after the filaments are passed through the drawing rollers 7.
  • the filaments can then be cooled through a cooling drum 9, and passed through intermingler 11 via roller 17, where the filaments are entangled. Thereafter, the filaments are wound with the use of a wind-up machine 15 via roller 13 and a
  • the filaments are drawn at a speed of greater than 3000 meters per minute (m/min.).
  • the draw speed can be greater than 3500 m/min., greater than 4000 m/min., greater than 5000 m/min., at least 5100 m/min. or even at least 5500 m/min.
  • the draw ratio of the filaments is controlled by adjusting the speeds of the supply roller 6 and/or draw rolls 7 until the break elongation of the filaments is preferably at least about 10%, more preferably at least 20% and preferably no more than about 90%, more preferably no more than 70%.
  • the drawn filament denier is greater than 1 , preferably at least 3, more preferably at least 10, most preferably at least about 15 dl/g.
  • the yarn denier is preferably greater than 210, more preferably at least about 250, even more preferably at least about 500 and most preferably at least about 1000.
  • a jet-bulking unit 8 where the filaments can be blown and deformed in three directions with hot bulking fluid such as air or steam can be used in practicing the invention.
  • a suitable unit is described in U.S. Pat. No. 3,525,134.
  • the filaments are both bulked and entangled.
  • Other bulking units can be used. With some units, a separate entangling step may be necessary prior to the windup. Any method common in the trade may be used to entangle the yarn.
  • the resultant BCF yarn having randomly spaced 3- dimensional curvilinear crimp, is then preferably cooled below the glass transition temperature of the filaments (approximately 45-50° C.) while the yarn is in a state of approximately 0 gpd tension so as not to pull out a significant amount of crimp. Cooling may be accomplished by a variety of commercially available means, preferably by air or water flow, spray or mist.
  • the filaments can be ply- twisted and heat set into yarn.
  • the yarn can then be made into carpet.
  • the yarn of the present invention could also be used in rugs, woven tiles, automotive interiors and fabrics.
  • melt stability was measured at 250 and 260 + 0.1 °C using a Dynisco LCR 7002 capillary rheometer with a 1 mm diameter, 30:1 L/D, 180 ° entrance angle die in accordance with test method ASTM D3835-02.
  • the melt stability was measured following procedure 10.8.1
  • Polymer solutions were injected into size exclusion chromatography system.
  • the system included size exclusion chromatography system Model Alliance 2690TM from Waters Corporation (Milford, MA), with a Waters 410TM refractive index detector (Differential Refractive Index) and Viscotek Corporation (Houston, TX) Model T-60ATM dual detector module incorporating static right angle light scattering and differential capillary viscometer detectors.
  • Columns for separation were Two Shodex GPC HFIP-80M TM styrene-divinyl benzene columns with exclusion limit 2 x 107 and 8,000/30cm theoretical plates. Chromatographic conditions were at 35°C temperature, 1.00 ml/min flow rate, 0.1 ml injection volume and 50 minute run time.
  • Poly (trimethylene terephthalate) polymer (3GT, PTT) in chip form was dried in a rotary dryer. Drying was done under vacuum at 160 degrees centigrade (° C ) for 6 hours, cooled with nitrogen gas to 25° C and stored in a sealed vessel to maintain a moisture level less than 50 ppm. For remelting, the chip was fed to a dry nitrogen supply hopper at room temperature and then gravity fed into the throat of the extruder.
  • An alternative method is to have a drier mounted above the extruder and continuously dry chip at 160° C for 6-8 hours using dry nitrogen or air. A dry nitrogen purge was located at the extruder throat to remove oxygen from the down coming chip when using dry air.
  • the single screw extruder was set at: Zonel 230° C Zone 2 240° C Zone 3 250° C Zone 4 250° C Zone 5 250° C Extruder speed 14 rpm Melt Pressure 80 bar
  • the extruder discharge melt temperature was 250° C
  • the transfer line and spin beam temperature was maintained at about 250° C.
  • the melted polymer was fed to a 2-pack spin beam.
  • the spin beam metering gear pumps provided 76 bar pressure to the spin pack. Each pump had a capacity of 30 cubic centimeters per revolution (cm 3 /rev). The pumps were run at 12.10 rpm.
  • Each pack had a 1 layer metal screen filter with a screen mesh size of 10,000 M/cm 2 .
  • the spinnerets each had 68 trilobal ( Y ) holes with capillary diameter of 0.35x0.66 mm with a length of 0.6 mm.
  • the extruded or spun filaments were quenched with 18° C air maintained at 80% humidity with a quench zone length of 1600 mm. Average air cross flow was 0.35 meters/second (m/s).
  • the filaments were pulled down through a one floor high interfloor tube (part of a 3 floor machine) to a Neumag Bulk Continuous Filament (BCF) spinning machine. At the bottom of the interfloor tube two sets of 68 filaments were converged using finish applicators.
  • the contact width of the upper applicators was 5 millimeters (mm) and the lower reversed finish applicators were 2 mm.
  • Two 4 stream 0.8 cm 3 /rev finish pumps set at 35 rpm pumped 18 % standard finish to the finish applicators.
  • the threadlines were led onto an inlet godet (roller) with a surface speed of 1950 meters per minute (m/min. ),then, onto a metering godet duo set at 40° C with a surface speed of 1970 m/min..
  • the filaments were drawn in space by advancing to a set of enclosed heated duos set at 165° C with a surface speed of 3742 m/min.
  • the filaments were heated by the godets fed into a Neumag texturing chamber that had a lamella cone of 3 / 4.5 mm and length of 80 mm. 18 lamella pieces formed the cone. Hot air set at 7.0 bar and 225° C impinged on the yarn bundles.
  • the lamella exhaust cone had a vacuum setting of -70 millibars (mbar).
  • the textured or bulked yarn flowed out of the bottom of the chamber and piddled onto a cooling drum with a surface speed of 60 m/min.
  • the cooled threadlines were removed from the cooling drum with a godet with a surface speed of 3010 m/min. From the godet the threadlines went through a tacking or intermingling box that had an air jet with a yoke width and diameter of 6 mm.
  • the threadlines were impinged with an air pressure of 5.5 bar.
  • the correct tension was controlled by an exit godet with a surface speed of 3030 m/min. This godet isolated the winding tension from the required tacking tension.
  • the threadlines were led to a two-cot winder that takes a tube diameter of 79 millimeters (mm).
  • the drive roll or pressure roll (set at 100 newtons (N)) surface speed was 3015 m/min., which produced a winding tension of around 150 grams.
  • the traversing stroke was 250 mm and was run at speed to produce a 13-degree winding angle.
  • the traversing mechanism was modulated with an amplitude of 0.1 % at 0.1 / second.
  • the final package diameter was 215 mm producing a package weight of 5.1 kilograms.
  • Poly (trimethylene terephthalate) polymer (3GT, PTT) in chip form was dried in a rotary dryer. Drying was done under vacuum at 160 degrees centigrade (° C ) for 6 hours, cooled with nitrogen gas to 25° C and stored in a sealed vessel to maintain a moisture level less than 50 ppm. For remelting, the chip was fed to a dry nitrogen supply hopper at room temperature and then gravity fed into the throat of the extruder.
  • An alternative method is to have a drier mounted above the extruder and continuously dry chip at 160° C for 6-8 hours using dry nitrogen or air. A dry nitrogen purge was located at the extruder throat to remove oxygen from the down coming chip when using dry air in the drier.
  • the single screw extruder was set at: Zonel 230° C Zone 2 240° C Zone 3 250° C Zone 4 250° C Zone 5 250° C Extruder speed 15 rpm Melt Pressure 80 bar
  • the extruder discharge melt temperature was 250° C.
  • the transfer line and spin beam temperature was maintained at 250° C.
  • the melted polymer was fed to a 2-pack spin beam.
  • In the spin beam metering gear pumps provided 79 bar pressure to the spin pack. Each pump had a capacity of 30 cm 3 /rev. The pumps were run at 13.26 rpm.
  • Each pack has a 1 layer metal screen filter with a screen mesh size of 10,000 M/cm 2 .
  • the spinnerets each have 68 trilobal ( Y ) holes with capillary diameter of
  • the cooled threadlines were removed from the cooling drum with a godet with a surface speed of 3300 m/min.. From the godet the threadlines went through a tacking or intermingling box that had an air jet with a yoke width and diameter of 6 mm. The threadlines were impinged with an air pressure of 7.0 bar. The correct tension was control by an exit godet with a surface speed of 3340 m/min.. This godet isolated the winding tension from the required tacking tension. The threadlines were led to a two-cot winder that took a tube diameter of 79 mm. The drive roll or pressure roll (set at 100 N) surface speed was 3305 m/min., which produces a winding tension of around 150 grams.
  • the traversing stroke was 250 mm and was run at speed to produce a 13-degree winding angle.
  • the traversing mechanism was modulated with an amplitude of 0.1% at 0.1 / second.
  • the final package diameter was 215 mm producing a package weight of 5.1 kilograms.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Fluid Mechanics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Artificial Filaments (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Carpets (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
PCT/US2005/000774 2004-01-06 2005-01-06 Process for preparing poly(trimethylene terephthalate) fiber WO2005068695A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
EP05711340A EP1702092A4 (en) 2004-01-06 2005-01-06 PROCESS FOR THE PREPARATION OF A POLY (TRIMETHYLENE TEREPHTHALATE) FIBER
MXPA06007683A MXPA06007683A (es) 2004-01-06 2005-01-06 Proceso para preparar fibra de poli(trimetilentereftalato).
CA002552662A CA2552662A1 (en) 2004-01-06 2005-01-06 Process for preparing poly(trimethylene terephthalate) fiber
JP2006549507A JP2007521422A (ja) 2004-01-06 2005-01-06 ポリ(トリメチレンテレフタレート)繊維の製造方法
CN200580001824XA CN1906340B (zh) 2004-01-06 2005-01-06 制备聚(对苯二甲酸1,3-丙二醇酯)纤维的方法以及用该纤维制成的地毯

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/752,399 2004-01-06
US10/752,399 US20050147784A1 (en) 2004-01-06 2004-01-06 Process for preparing poly(trimethylene terephthalate) fiber

Publications (1)

Publication Number Publication Date
WO2005068695A1 true WO2005068695A1 (en) 2005-07-28

Family

ID=34711624

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2005/000774 WO2005068695A1 (en) 2004-01-06 2005-01-06 Process for preparing poly(trimethylene terephthalate) fiber

Country Status (9)

Country Link
US (1) US20050147784A1 (zh)
EP (1) EP1702092A4 (zh)
JP (1) JP2007521422A (zh)
KR (1) KR20060123432A (zh)
CN (1) CN1906340B (zh)
CA (1) CA2552662A1 (zh)
MX (1) MXPA06007683A (zh)
TW (1) TW200602525A (zh)
WO (1) WO2005068695A1 (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102618947A (zh) * 2012-04-06 2012-08-01 缪爱国 Ptt螺旋型三维中空纤维的生产方法

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8015726B2 (en) * 2005-06-23 2011-09-13 Whirlpool Corporation Automatic clothes dryer
US8021736B2 (en) * 2006-07-13 2011-09-20 E.I. Du Pont De Nemours And Company Substantially flame retardant-free 3GT carpet
ATE540144T1 (de) * 2008-05-23 2012-01-15 Oerlikon Textile Gmbh & Co Kg Verfahren zum schmelzspinnen, verstrecken und aufwickeln eines multifilen fadens sowie eine vorrichtung zur durchführung des verfahrens
CN101735608B (zh) * 2009-12-14 2011-07-20 杭州师范大学 吸湿性细旦/超细旦锦纶母粒、锦纶poy长丝及其制备方法
EP2659037B1 (en) * 2010-12-28 2017-07-26 E. I. du Pont de Nemours and Company Carpets prepared from yarns comprising a fluorinated polyester blend
CN102758604B (zh) * 2012-07-30 2014-12-17 中国石油集团川庆钻探工程有限公司长庆井下技术作业公司 压裂施工纤维的膨化技术
DE102017100487A1 (de) * 2017-01-12 2018-07-12 Trützschler GmbH & Co Kommanditgesellschaft Vorrichtung und Verfahren zur Erzeugung eines mehrfarbigen Garnes
DE102017100488A1 (de) 2017-01-12 2018-07-12 Trützschler GmbH & Co Kommanditgesellschaft Vorrichtung und Verfahren zur Erzeugung eines texturierten Filamentes oder Garnes

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996000808A1 (en) * 1994-06-30 1996-01-11 E.I. Du Pont De Nemours And Company Process for making poly(trimethylene terephthalate) bulked continuous filaments, the filaments thereof and carpets made therefrom
US20020132116A1 (en) * 2000-11-03 2002-09-19 Dietmar Wandel Method of spinning, spooling, and stretch texturing polyester filaments and polyesters thereby produced
US20020130433A1 (en) * 2000-10-10 2002-09-19 Hwo Charles Chiu-Hsiung Spin draw process of making partially oriented yarns from polytrimethylene terephthalate
US20020147298A1 (en) * 1999-11-12 2002-10-10 Yanhui Sun Polyamide compounds

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3525134A (en) * 1969-02-17 1970-08-25 Du Pont Yarn fluid treating apparatus
US3998042A (en) * 1972-09-26 1976-12-21 E. I. Du Pont De Nemours And Company Mixed shrinkage yarn
US6113825A (en) * 1995-05-08 2000-09-05 Shell Oil Company Process for preparing poly(trimethylene terephthalate) carpet yarn
US6315934B1 (en) * 1995-05-08 2001-11-13 Shell Oil Company Process for preparing poly(thimethylene therephthalate) carpet yarn
TR199600362A2 (tr) * 1995-05-08 1996-11-21 Shell Int Research Poli(trimetilen tereftalat) ipliklerin hazirlanmasi icin usul.
US6242558B1 (en) * 1996-11-27 2001-06-05 Shell Oil Company Modified polytrimethylene terephthalate
US6093786A (en) * 1996-11-27 2000-07-25 Shell Oil Company Process for preparing polytrimethylene terephthalate
US5804115A (en) * 1996-12-13 1998-09-08 Basf Corporation One step, ready-to-tuft, mock space-dyed multifilament yarn
DE19705249A1 (de) * 1997-02-12 1998-08-13 Zimmer Ag Verfahren zur Herstellung von Polypropylenterphthalat
US6652964B1 (en) * 1997-08-18 2003-11-25 Asahi Kasei Kabushiki Kaisha Polyester fiber and fabric prepared therefrom
WO1999011709A1 (fr) * 1997-09-03 1999-03-11 Asahi Kasei Kogyo Kabushiki Kaisha Composition a base de resine polyester
US6284370B1 (en) * 1997-11-26 2001-09-04 Asahi Kasei Kabushiki Kaisha Polyester fiber with excellent processability and process for producing the same
US5840957A (en) * 1998-03-16 1998-11-24 E. I. Du Pont De Nemours And Company Transesterification process using lanthanum compound catalyst
US6109015A (en) * 1998-04-09 2000-08-29 Prisma Fibers, Inc. Process for making poly(trimethylene terephthalate) yarn
US5994451A (en) * 1998-04-24 1999-11-30 Shell Oil Company Polytrimethylene terephthalate composition
MXPA01003740A (es) * 1998-10-15 2004-09-10 Asahi Chemical Ind Fibra politrimetilentereftalato.
ATE330995T1 (de) * 1998-10-30 2006-07-15 Asahi Chemical Ind Polyesterharz-zusammensetzung und fasern
BR0008986A (pt) * 1999-03-15 2002-01-22 Asahi Chemical Ind Fibra de tereftalato de politrimetileno torcida ou não torcida, com alta uniformidade, e, processo para produzir a mesma
US6350895B1 (en) * 1999-03-26 2002-02-26 E. I. Du Pont De Nemours And Company Transesterification process using yttrium and samarium compound catalystis
US6331264B1 (en) * 1999-03-31 2001-12-18 E. I. Du Pont De Nemours And Company Low emission polymer compositions
ATE234336T1 (de) * 1999-04-22 2003-03-15 Zimmer Ag Verfahren zur herstellung von polytrimethylenterephthalat (ptt)
US6512080B2 (en) * 1999-04-22 2003-01-28 Shell Oil Company Process of producing polytrimethylene terephthalate (PTT)
US6277947B1 (en) * 2000-04-21 2001-08-21 Shell Oil Company Process of producing polytrimethylene terephthalate (PTT)
US6297315B1 (en) * 1999-05-11 2001-10-02 Shell Oil Company Process for preparing polytrimethylene terephthalate
TW522179B (en) * 1999-07-12 2003-03-01 Asahi Chemical Ind Polyester yarn and producing method thereof
DE19934551A1 (de) * 1999-07-22 2001-01-25 Lurgi Zimmer Ag PTT-Stapelfasern und Verfahren zu ihrer Herstellung
DE19937729A1 (de) * 1999-08-10 2001-02-15 Lurgi Zimmer Ag Hochfeste Polyesterfäden und Verfahren zu deren Herstellung
EP1206497A1 (en) * 1999-08-25 2002-05-22 E.I. Du Pont De Nemours And Company Preparation of poly(trimethylene terephthalate) with low level of di(1,3-propylene glycol)
TW476820B (en) * 1999-09-30 2002-02-21 Asahi Chemical Ind Polytrimethyleneterephthalate multifilament yarn
US6255442B1 (en) * 2000-02-08 2001-07-03 E. I. Du Pont De Nemours And Company Esterification process
EP1259558B2 (en) * 2000-02-11 2010-04-21 E.I. Du Pont De Nemours And Company Continuous process for producing poly(trimethylene terephthalate)
US6353062B1 (en) * 2000-02-11 2002-03-05 E. I. Du Pont De Nemours And Company Continuous process for producing poly(trimethylene terephthalate)
US6528579B2 (en) * 2000-02-17 2003-03-04 Shell Oil Company Zero-heel polyester process
EP1183409B1 (en) * 2000-03-03 2005-11-16 E.I. Du Pont De Nemours And Company Poly(trimethylene terephthalate) yarn
US6663806B2 (en) * 2000-03-03 2003-12-16 E. I. Du Pont De Nemours And Company Processes for making poly (trimethylene terephthalate) yarns
US6287688B1 (en) * 2000-03-03 2001-09-11 E. I. Du Pont De Nemours And Company Partially oriented poly(trimethylene terephthalate) yarn
JP3856617B2 (ja) * 2000-04-04 2006-12-13 帝人ファイバー株式会社 仮撚加工用ポリエステル繊維
MY127766A (en) * 2000-04-21 2006-12-29 Shell Int Research Optimum dipropylene glycol content polytrimethylene terephthalate compositions
GB2361925A (en) * 2000-05-02 2001-11-07 Shell Internat Res Maatschhapp High temperature solid state polymerisation of poly(trimethylene terephthalate)
CN1178833C (zh) * 2000-05-12 2004-12-08 旭化成株式会社 预取向丝卷装、其制造法以及假捻加工法
US6667003B2 (en) * 2000-05-25 2003-12-23 Zimmer A.G. Method for the manufacture of synthetic fibers from a melt mixture based on fiber forming polymers
AU2001269458A1 (en) * 2000-07-06 2002-01-21 Asahi Kasei Kabushiki Kaisha Drawn yarn package and production method therefor
US20020116802A1 (en) * 2000-07-14 2002-08-29 Marc Moerman Soft and stretchable textile fabrics made from polytrimethylene terephthalate
KR100339275B1 (ko) * 2000-07-21 2002-06-03 조정래 이염성(易染性) 폴리에스테르 섬유
US6403762B1 (en) * 2000-08-21 2002-06-11 Shell Oil Company Solid state polymerization process for poly(trimethylene terephthalate) utilizing a combined crystallization/preheating step
US6872352B2 (en) * 2000-09-12 2005-03-29 E. I. Du Pont De Nemours And Company Process of making web or fiberfill from polytrimethylene terephthalate staple fibers
US6702864B2 (en) * 2000-10-11 2004-03-09 Shell Oil Company Process for making high stretch and elastic knitted fabrics from polytrimethylene terephthalate
US20020130437A1 (en) * 2000-11-03 2002-09-19 Dietmar Wandel Method of spinning, spooling, and stretch texturing Polyester filaments and polyesters thereby produced
US20030004301A1 (en) * 2000-11-03 2003-01-02 Dietmar Wandel Method of spinning, spooling, and stretch texturing polyester filaments and polyester filaments thereby produced
US6667096B2 (en) * 2000-11-03 2003-12-23 Zimmer A.G. Method of spinning, spooling, and stretch texturing polyester filaments and polyester filaments produced
US6740400B2 (en) * 2001-02-07 2004-05-25 Asahi Kasei Kabushiki Kaisha Poly (trimethylene terephthalate) and a process for producing the same
KR100397621B1 (ko) * 2001-05-14 2003-09-13 주식회사 효성 카페트용 폴리(트리메틸렌 테레프탈레이트) bcf이형단면사
KR100397620B1 (ko) * 2001-05-14 2003-09-13 주식회사 효성 폴리(트리메틸렌 테레프탈레이트) 카페트의 제조방법
DE10125677B4 (de) * 2001-05-25 2013-05-16 Lurgi Zimmer Gmbh Verfahren und Vorrichtung zur Herstellung von Polytrimethylenterephthalat
TW584645B (en) * 2001-06-01 2004-04-21 Robert Lawrence Blackbourn A method for producing polytrimethylene terephthalate
US6740276B2 (en) * 2001-06-29 2004-05-25 E. I. Du Pont De Nemours And Company Process for preparing pigmented shaped articles comprising poly (trimethylene terephthalate)
JP3970245B2 (ja) * 2001-10-11 2007-09-05 旭化成せんい株式会社 ポリトリメチレンテレフタレートのペレットおよびその製造方法
JP3862996B2 (ja) * 2001-10-31 2006-12-27 帝人ファイバー株式会社 ポリトリメチレンテレフタレートフィラメント糸およびその製造方法
US6740733B2 (en) * 2001-11-30 2004-05-25 Shell Oil Company Process and apparatus for crystallization of polytrimethylene terephthalate (PTT)
TWI287053B (en) * 2002-02-20 2007-09-21 Shell Int Research A process for making stable polytrimethylene terephthalate packages
US20030175522A1 (en) * 2002-03-13 2003-09-18 Kurian Joseph Varapadavil Poly(trimethylene terephthalate) carpets
US20030111171A1 (en) * 2002-09-09 2003-06-19 Casey Paul Karol Poly(trimethylene) terephthalate texile staple production

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996000808A1 (en) * 1994-06-30 1996-01-11 E.I. Du Pont De Nemours And Company Process for making poly(trimethylene terephthalate) bulked continuous filaments, the filaments thereof and carpets made therefrom
US20020147298A1 (en) * 1999-11-12 2002-10-10 Yanhui Sun Polyamide compounds
US20020130433A1 (en) * 2000-10-10 2002-09-19 Hwo Charles Chiu-Hsiung Spin draw process of making partially oriented yarns from polytrimethylene terephthalate
US20020132116A1 (en) * 2000-11-03 2002-09-19 Dietmar Wandel Method of spinning, spooling, and stretch texturing polyester filaments and polyesters thereby produced

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102618947A (zh) * 2012-04-06 2012-08-01 缪爱国 Ptt螺旋型三维中空纤维的生产方法

Also Published As

Publication number Publication date
JP2007521422A (ja) 2007-08-02
TW200602525A (en) 2006-01-16
EP1702092A4 (en) 2007-12-05
CN1906340A (zh) 2007-01-31
KR20060123432A (ko) 2006-12-01
MXPA06007683A (es) 2006-09-01
CN1906340B (zh) 2012-07-04
US20050147784A1 (en) 2005-07-07
EP1702092A1 (en) 2006-09-20
CA2552662A1 (en) 2005-07-28

Similar Documents

Publication Publication Date Title
EP1702092A1 (en) Process for preparing poly(trimethylene terephthalate) fiber
JP5247860B2 (ja) 2成分繊維の高速紡糸方法
EP0745711B1 (en) Process for preparing poly (trimethylene terephthalate) yarns
US6113825A (en) Process for preparing poly(trimethylene terephthalate) carpet yarn
EP1283285B1 (en) Poly(lactic acid) fiber
MXPA02007125A (es) Metodo para el hilado a alta velocidad de fibras bicompuestas.
EP1573099B1 (en) Shaped articles with improved stability
JPH0355566B2 (zh)
CN1239763C (zh) 聚对苯二甲酸丙二醇酯细旦纱
CN1066212C (zh) 制造连续聚酯长丝纱的方法及该长丝纱的用途
US6315934B1 (en) Process for preparing poly(thimethylene therephthalate) carpet yarn
EP1299580B1 (en) Method of producing polymeric filaments
US20090146338A1 (en) Process for preparing polymer fibers
EP1350874A1 (en) Bulky polyester multifilament composite yarn and process for producing the same
JP4270734B2 (ja) 嵩高性を有する生分解性繊維の製造方法
EA003951B1 (ru) Способ формования и намотки полиэфирных мононитей, полученные способом формования полиэфирные мононити, текстурирование полиэфирных мононитей в процессе вытягивания и полученные текстурированием в процессе вытягивания объемные полиэфирные мононити
CN1320178C (zh) 聚对苯二甲酸丙二酯稳定卷装的制造方法
Gupta et al. Poly (ethylene terephthalate) fibres
KR20140093992A (ko) 폴리(트라이메틸렌 테레프탈레이트)를 포함하는 2성분 섬유의 제조 공정
KR20190080453A (ko) 점도 편차가 개선된 산업용 폴리에스테르 원사의 제조방법

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200580001824.X

Country of ref document: CN

AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 3146/DELNP/2006

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2005711340

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2552662

Country of ref document: CA

Ref document number: PA/a/2006/007683

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 1020067013476

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2006549507

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Ref document number: DE

WWP Wipo information: published in national office

Ref document number: 2005711340

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 1020067013476

Country of ref document: KR