US20050147784A1 - Process for preparing poly(trimethylene terephthalate) fiber - Google Patents
Process for preparing poly(trimethylene terephthalate) fiber Download PDFInfo
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- US20050147784A1 US20050147784A1 US10/752,399 US75239904A US2005147784A1 US 20050147784 A1 US20050147784 A1 US 20050147784A1 US 75239904 A US75239904 A US 75239904A US 2005147784 A1 US2005147784 A1 US 2005147784A1
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- filaments
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- yarn
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G1/00—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
- D02G1/02—Producing 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
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G1/00—Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
- D02G1/20—Combinations of two or more of the above-mentioned operations or devices; After-treatments for fixing crimp or curl
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02J—FINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
- D02J1/00—Modifying 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
- D02J1/08—Interlacing constituent filaments without breakage thereof, e.g. by use of turbulent air streams
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/04—Fibres 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]
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2503/00—Domestic or personal
- D10B2503/04—Floor or wall coverings; Carpets
Definitions
- the present invention relates to a polyester yarn and its manufacture. More particularly, the invention relates to a process for producing poly(trimethylene terephthalate) fibers having good physical properties.
- Polyethylene terephthalate (“2GT”) and polybutylene terephthalate (“4GT”), generally referred to as “polyalkylene terephthalates”, are common commercial polyesters.
- Polyalkylene terephthalates have excellent physical and chemical properties, in particular, chemical, heat and light stability, high melting points and high strength. As a result they have been widely used for resins, films and fibers.
- 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
- 4,877,572 describes a process for preparing poly(butylene terephthalate) BCF yarn in which the extruded fiber is drawn in one stage, the feed roller being heated to a temperature 30° C. above or below the Tg of the polymer and the draw roller being at least 100° C. higher than the feed roller.
- U.S. Pat. No. 6,254,961 relates to spinning poly(trimethylene terephthalate) into yarn suitable for carpets. According to this patent, drawing speeds of greater than 1000 m/min. are possible with the inventive process, with drawing speeds greater than 1800 m/min. desirable because of the high tenacity of the resulting yarn.
- 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 single filament size is not restricted, it is from 0.1 to 10 d, preferably from 0.5 to 5 d, more preferably from 1 to 3 d. Also according to this patent, it is important that the peripheral speed of a first roll used to produce the fiber be from 300 to 3,500 m/min. The peripheral speed is preferably from 800 to 3,000 m/min, more preferably from 1,200 to 2,500 m/min. Although the peripheral speed of a second roll is determined by the draw ratio, it is usually from 600 to 6,000 m/min.
- U.S. patent Pub. No. 2003/0127766 relates, in general, to a poly(trimethylene terephthalate) BCF carpet modified cross-section yarn and a method for preparing the same and in particular, to a poly(trimethylene terephthalate) BCF carpet modified cross-section yarn and a method for preparing the same.
- poly(trimethylene terephthalate) with an intrinsic viscosity of 0.8 to 1.2 and a moisture content of 50 ppm or less is used as raw materials, and preferably melt-spun at a spinning rate of 1500 to 4000 m/min. Spun filaments are drawn at a rate of 1500 to 4000 m/min. and crimped.
- U.S. patent Pub. No. 2003/0045611 relates to a process for preparation of pigmented shaped articles (e.g., fibers).
- poly(trimethylene terephthalate) preferably has an intrinsic viscosity that is about 0.6 dl/g or higher, and typically is about 1.5 dl/g or less.
- Preferred viscosities for many end uses, and, particularly for fibers and films, are 0.8 dl/g or higher, more preferably 0.9 dl/g or higher.
- the viscosity of poly(trimethylene terephthalate) fibers and films is 1.4 dl/g or less, 1.2 dl/g or less, or 1.1 dl/g or less.
- the spinning speed is preferably at least about 1,000 meters/minute, and may be up to about 5,000 meters/minute or more, using roll 40 as reference speed.
- a process comprises:
- the filaments are drawn at a draw ratio of about 1.1 to about 4.0.
- the poly(trimethylene terephthalate) has an intrinsic viscosity of about 0.95 to about 1.10.
- the drawn filaments can be bulked and/or entangled. They can be bulked to form 3-dimensional curvilinear crimp therein.
- the bulking comprises blowing and deforming the filaments in a hot-fluid jet bulking unit.
- a process comprises:
- the bulked continuous filaments are entangled before the cooling.
- the filaments can be ply-twisted and heat set into a yarn.
- the ply-twisted, heat-set yarn can be made into carpet.
- FIG. 1 schematically illustrates a chip dryer and melt extruder system
- FIG. 2 schematically illustrates a spinning configuration useful in this invention.
- a process comprises:
- the filaments can be coated with a spin finish and, optionally, preintermingled.
- the process further comprises bulking the drawn filaments.
- the drawn filaments can be bulked to form 3-dimensional curvilinear crimp therein.
- the bulking comprises blowing and deforming the filaments in a hot-fluid jet bulking unit.
- the process further comprises entangling the filaments.
- a process comprises:
- the bulked continuous filaments can be entangled before the cooling.
- the filaments are ply-twisted and heat set into yarn.
- Carpet can be made from the ply-twisted and heat-set yarn.
- poly(trimethylene terephthalate) chips are loaded into dryer 10 to be dried.
- the intrinsic viscosity of the poly(trimethylene terephthalate) is preferably about 0.95 to about 1.10 dl/g.
- the intrinsic viscosity can be about 0.98 to about 1.04 or about 1.00 to about 1.02.
- the number average molecular weight is at least about 26500, more preferable at least about 27500, most preferably, at least about 29000.
- the number average molecular weight is up to about 50000, more preferably up to about 45000, most preferably up to about 40000.
- 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. Also preferably, 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.
- the poly(trimethylene terephthalate) chips are preferably dried until the moisture content is less than 100 ppm, more preferably about 50 ppm or less, and most preferably about 40 ppm or less. Drying time should be as long as required to reach the desired moisture content, preferably about 4 to about 10 hours, more preferably about 6 to about 8 hours.
- the operator should keep the moisture level steady in order to maintain consistent melt viscosity.
- Commercially available dehumidifiers can be used. Dry nitrogen, air or other inert gasses can be used.
- the dried chips are fed to an optional chip metering screw 12 and are metered in to the remelter throat 14 .
- the metering screw is optional since the screw can be used to control the amount of chips used.
- a chip metering screw is normally used with a screw remelter. Any commercially available metering screw can be used.
- remelter throat reference is being made to a pipe connecting the metering screw and the remelter.
- the remelter can be any suitable single or twin screw extruder.
- a nitrogen purge can be used to prevent oxygen from being carried along with the chips into the remelter. This will reduce oxygen-caused polymer degradation.
- Remelting is preferably carried out at about 200° C. or higher, preferably at least about 235° C., more preferably at least about 245° C., and at about 2800 C. or lower, preferably about 270° C. or lower, more preferably about 265° C. or lower. At temperatures above 280° C., the undesirable byproduct acrolein is generated.
- Polymer is fed to optional transfer line pump 20 , which provides sufficient pressure (about 2250-3000 psig) to overcome losses in the transfer line 22 , provide constant feed rate, and provide sufficient pressure to feed the polymer to the spin pack metering pump 24 .
- transfer line pump 20 provides sufficient pressure (about 2250-3000 psig) to overcome losses in the transfer line 22 , provide constant feed rate, and provide sufficient pressure to feed the polymer to the spin pack metering pump 24 . Any suitable pump may be used.
- Transfer line 22 is, preferably, surrounded by an outer pipe (not shown), which provides an outer jacket for the transfer line.
- the outer jacket can contain heat transfer fluid to help maintain the temperature of the polymer within acceptable limits.
- the temperature of the polymer transfer line 22 is preferably kept at least at about 220° C., more preferably at least at about 230° C., most preferably at least about 240° C.
- the temperature can be up to about 265° C., preferably up to about 260° C., most preferably up to about 255° C.
- the heat transfer fluid in the jacket could be paraffin kept, preferably, below 250° 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 .
- the filaments can be treated with turbulent air in the optional preintermingling device 5 to even out the finish on the filaments.
- the polymer is extruded through the spinneret or die at a temperature of at least about 200° C., preferably at least about 235° C., more preferably at least about 245° C., and up to about 275° C., preferably up to about 270° C., more preferably up to about 265° C.
- 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. As shown, the filaments are converged into yarn at roller 6 .
- gas typically humidified air
- 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 yarn guide 16 .
- 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 disclosure of which is hereby incorporated herein by reference.
- the filaments are both bulked and entangled.
- 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.
- Poly(trimethylene terephthalate) (3GT) resins were dried at 120° C. for 50 hours under vacuum with a heated, dry nitrogen sweep using a VWR Model 1430M vacuum oven.
- the moisture level in the dried resins was measured at 180° C. with 10 minute delay time using a Mitsubishi Moisture Analyzer Model CA100 with a Vaporizer Model VA100.
- the moisture levels in the 3GT Sample 1 and 3GT Sample 2 were 38 and 40 ppm, respectively.
- melt stability and melt viscosity were measured at 250 and 260 ⁇ 0.1° C. using a Dynisco LCR 7002 capillary rheometer with a 1 mm diameter, 30:1 LID, 180° entrance angle die in accordance with test method ASTM D3835-02.
- the melt stability was measured following procedure 10.8.1 ASTM D3835-02. A constant rate test at 48.6 s ⁇ 1 was used with a delay time of at least 1200 seconds. Extrudate samples were collected at 40, 120, 180, 250, 360, 600, 900, and 1200 seconds. The Goodyear IV of the as-received resins and extrudates were measured in 50/50 wt % trifluoroacetic acid/dichloromethane at 19° C. and a concentration of 0.4 g/dl using a Viscotek Forced Flow Viscometer Model Y-900, V5.7.
- the melt viscosity was measured following procedure 10.8.2. ASTM D3835-02. A multiple rate test with software detection of steady state (procedure X2) of ASTM D3835-02.was used with a melt time of 300 seconds and a shear rate of 48.6 s ⁇ 1 repeated at the beginning, middle and end of each test.
- the melt viscosity stability was determined from the slope of the best-fit line through a plot of the repeated viscosity values versus dwell time (procedure X1.4) of ASTM D3835-02. The melt viscosity stability was used to correct the data at each shear rate to zero dwell time.
- Polymer solutions were injected into size exclusion chromatography system.
- the system included size exclusion chromatography system Model Alliance 2690TM from Waters Corporation (Milford, Mass.), with a Waters 410TM refractive index detector (Differential Refractive Index) and Viscotek Corporation (Houston, Tex.) Model T-60ATM dual detector module incorporating static right angle light scattering and differential capillary viscometer detectors.
- Columns for seperation were Two Shodex GPC HFIP-80M TM styrene-divinyl benzene columns with exclusion limit 2 ⁇ 107 and 8,000/30 cm 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: Zone 1 230° 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 0.35 ⁇ 0.66 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.
- 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: Zone 1 230° 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.
- 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 0.35 ⁇ 0.66 millimeters (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 0.25 meter per second (m/s).
- the filaments were pulled down through a one floor high interfloor tube (part of a 3 floor machine) to a Neumag spinning machine. At the bottom of the interfloor tube the two sets of 68 filaments were converged using finish applicators.
- the contact width of the upper applicators was 5 mm and the lower reversed finish applicators were 2 mm.
- Two 4 stream 0.8 cm3/rev finish pumps set at 40 rpm pumped P-7050T18 % Fiber Solutions finish to the finish applicators.
- the threadlines were led onto an inlet godet with a surface speed of 2390 m/min. Then, onto a metering godet duo set at 40° C. with a surface speed of 2400 m/min.
- the filaments were drawn in space with no assist by advancing to a set of enclosed heated duos set at 165° C. with a surface speed of 4100 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 7.5 bar and 225° C. impinged on the yarn bundles.
- the lamella exhaust cone had a vacuum setting of ⁇ 95 m/bar.
- the textured or bulked yarn flowed out of the bottom of the chamber and piddled onto a cooling drum with a surface speed of 65 m/min.
- 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.
Abstract
The present invention relates to a process for spinning poly(trimethylene terephthalate) filaments/yarn. The poly(trimethylene terephthalate) has a number average molecular weight of at least about 26500 and a melt viscosity of at least about 350 Pascals at 250° C. and 48.65 per second shear rate. It is spun and the filaments are converged into yarn. The filaments have a denier greater than 1 and the yarn has a denier greater than 210.
Description
- The present invention relates to a polyester yarn and its manufacture. More particularly, the invention relates to a process for producing poly(trimethylene terephthalate) fibers having good physical properties.
- Polyethylene terephthalate (“2GT”) and polybutylene terephthalate (“4GT”), generally referred to as “polyalkylene terephthalates”, are common commercial polyesters. Polyalkylene terephthalates have excellent physical and chemical properties, in particular, chemical, heat and light stability, high melting points and high strength. As a result they have been widely used for resins, films and fibers.
- 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. U.S. Pat. No. 4,877,572 describes a process for preparing poly(butylene terephthalate) BCF yarn in which the extruded fiber is drawn in one stage, the feed roller being heated to a temperature 30° C. above or below the Tg of the polymer and the draw roller being at least 100° C. higher than the feed roller.
- U.S. Pat. No. 6,254,961 relates to spinning poly(trimethylene terephthalate) into yarn suitable for carpets. According to this patent, drawing speeds of greater than 1000 m/min. are possible with the inventive process, with drawing speeds greater than 1800 m/min. desirable because of the high tenacity of the resulting yarn.
- 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. According to this reference, 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. Although the single filament size is not restricted, it is from 0.1 to 10 d, preferably from 0.5 to 5 d, more preferably from 1 to 3 d. Also according to this patent, it is important that the peripheral speed of a first roll used to produce the fiber be from 300 to 3,500 m/min. The peripheral speed is preferably from 800 to 3,000 m/min, more preferably from 1,200 to 2,500 m/min. Although the peripheral speed of a second roll is determined by the draw ratio, it is usually from 600 to 6,000 m/min.
- U.S. patent Pub. No. 2003/0127766 relates, in general, to a poly(trimethylene terephthalate) BCF carpet modified cross-section yarn and a method for preparing the same and in particular, to a poly(trimethylene terephthalate) BCF carpet modified cross-section yarn and a method for preparing the same. According to this reference, poly(trimethylene terephthalate) with an intrinsic viscosity of 0.8 to 1.2 and a moisture content of 50 ppm or less is used as raw materials, and preferably melt-spun at a spinning rate of 1500 to 4000 m/min. Spun filaments are drawn at a rate of 1500 to 4000 m/min. and crimped.
- U.S. patent Pub. No. 2003/0045611 relates to a process for preparation of pigmented shaped articles (e.g., fibers). For fiber use, poly(trimethylene terephthalate) preferably has an intrinsic viscosity that is about 0.6 dl/g or higher, and typically is about 1.5 dl/g or less. Preferred viscosities for many end uses, and, particularly for fibers and films, are 0.8 dl/g or higher, more preferably 0.9 dl/g or higher. Typically, the viscosity of poly(trimethylene terephthalate) fibers and films is 1.4 dl/g or less, 1.2 dl/g or less, or 1.1 dl/g or less. In commercial applications, the spinning speed is preferably at least about 1,000 meters/minute, and may be up to about 5,000 meters/minute or more, using roll 40 as reference speed.
- According to a first aspect in accordance with the present invention a process comprises:
-
- (a) spinning molten poly(trimethylene terephthalate)polymer having a number average molecular weight of at least about 26500 and a melt viscosity of at least about 350 Pascals at 250° C. and 48.65 per second shear rate;
- (b) converging the filaments into yarn;
- (c) cooling the filaments; and
- (d) drawing the filaments at a speed of greater than 3000 meters per minute to produce filaments having a filament denier greater than 1, and a yarn denier greater than 210.
- Preferably, the filaments are drawn at a draw ratio of about 1.1 to about 4.0.
- Preferably, the poly(trimethylene terephthalate) has an intrinsic viscosity of about 0.95 to about 1.10.
- The drawn filaments can be bulked and/or entangled. They can be bulked to form 3-dimensional curvilinear crimp therein. Preferably, the bulking comprises blowing and deforming the filaments in a hot-fluid jet bulking unit.
- According to another aspect, 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;
- (g) bulking the drawn filaments such that the filaments are blown and deformed in three dimensions with a hot bulking fluid to form bulked continuous filaments having random 3-dimensional curvilinear crimp;
- (h) cooling the bulked continuous filaments to a temperature less than the glass transition temperature of the polymer filaments; and
- (i) entangling the bulked continuous filaments.
- Preferably, the bulked continuous filaments are entangled before the cooling. In another aspect, the filaments can be ply-twisted and heat set into a yarn. The ply-twisted, heat-set yarn can be made into carpet.
- The drawings are provided for illustration purposes only, and are not intended to limit the scope of the present invention.
-
FIG. 1 schematically illustrates a chip dryer and melt extruder system; and -
FIG. 2 schematically illustrates a spinning configuration useful in this invention. - Unless stated otherwise, all percentages, parts, ratios, etc., are by weight. Trademarks are shown in upper case.
- All patents, patent applications, and publications referred to herein are incorporated by reference in their entirety.
- Further, when an amount, concentration, or other value or parameter is given as either a range, preferred range or a list of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. Where a range of numerical values is recited herein, unless otherwise stated, the range is intended to include the endpoints thereof, and all integers and fractions within the range. It is not intended that the scope of the invention be limited to the specific values recited when defining a range.
- In accordance with a first aspect of the present invention, a process comprises:
-
- (a) spinning molten poly(trimethylene terephthalate)polymer having a number average molecular weight of at least about 26500 and a melt viscosity of at least about 350 Pascals at 250° C. and 48.65 per second shear rate;
- (b) converging the filaments into yarn;
- (c) cooling the filaments; and
- (d) drawing the 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 filaments can be coated with a spin finish and, optionally, preintermingled. Preferably, the process further comprises bulking the drawn filaments. The drawn filaments can be bulked to form 3-dimensional curvilinear crimp therein. Preferably, the bulking comprises blowing and deforming the filaments in a hot-fluid jet bulking unit.
- Preferably, the process further comprises entangling the filaments.
- According to a further aspect in accordance with the present invention, 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;
- (g) bulking the drawn filaments such that the filaments are blown and deformed in three dimensions with a hot bulking fluid to form bulked continuous filaments having random 3-dimensional curvilinear crimp;
- (h) cooling the bulked continuous filaments to a temperature less than the glass transition temperature of the polymer filaments; and
- (i) entangling the bulked continuous filaments.
- As noted, the bulked continuous filaments can be entangled before the cooling.
- According to a further aspect, the filaments are ply-twisted and heat set into yarn. Carpet can be made from the ply-twisted and heat-set yarn.
- With specific reference to
FIG. 1 of the drawing, poly(trimethylene terephthalate) chips are loaded intodryer 10 to be dried. The intrinsic viscosity of the poly(trimethylene terephthalate) is preferably about 0.95 to about 1.10 dl/g. The intrinsic viscosity can be about 0.98 to about 1.04 or about 1.00 to about 1.02. Preferably, the number average molecular weight is at least about 26500, more preferable at least about 27500, most preferably, at least about 29000. Preferably, the number average molecular weight is up to about 50000, more preferably up to about 45000, most preferably up to about 40000. Preferably, 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. Also preferably, 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. The poly(trimethylene terephthalate) chips are preferably dried until the moisture content is less than 100 ppm, more preferably about 50 ppm or less, and most preferably about 40 ppm or less. Drying time should be as long as required to reach the desired moisture content, preferably about 4 to about 10 hours, more preferably about 6 to about 8 hours. The operator should keep the moisture level steady in order to maintain consistent melt viscosity. Commercially available dehumidifiers can be used. Dry nitrogen, air or other inert gasses can be used. When the moisture content is at the desired level at the dryer exit, remelting is started.
- The dried chips are fed to an optional
chip metering screw 12 and are metered in to theremelter throat 14. - The metering screw is optional since the screw can be used to control the amount of chips used. A chip metering screw is normally used with a screw remelter. Any commercially available metering screw can be used.
- By “remelter throat” reference is being made to a pipe connecting the metering screw and the remelter.
- The remelter can be any suitable single or twin screw extruder. A nitrogen purge can be used to prevent oxygen from being carried along with the chips into the remelter. This will reduce oxygen-caused polymer degradation.
- Remelting is preferably carried out at about 200° C. or higher, preferably at least about 235° C., more preferably at least about 245° C., and at about 2800 C. or lower, preferably about 270° C. or lower, more preferably about 265° C. or lower. At temperatures above 280° C., the undesirable byproduct acrolein is generated.
- Polymer is fed to optional transfer line pump 20, which provides sufficient pressure (about 2250-3000 psig) to overcome losses in the
transfer line 22, provide constant feed rate, and provide sufficient pressure to feed the polymer to the spinpack metering pump 24. Any suitable pump may be used. - Polymer temperature should be monitored and controlled, using techniques well within the skill of the art, to prevent polymer degradation and possible generation of irritating and/or toxic byproducts.
Transfer line 22 is, preferably, surrounded by an outer pipe (not shown), which provides an outer jacket for the transfer line. The outer jacket can contain heat transfer fluid to help maintain the temperature of the polymer within acceptable limits. The temperature of thepolymer transfer line 22 is preferably kept at least at about 220° C., more preferably at least at about 230° C., most preferably at least about 240° C. The temperature can be up to about 265° C., preferably up to about 260° C., most preferably up to about 255° C. By way of non-limiting example, the heat transfer fluid in the jacket could be paraffin kept, preferably, below 250° 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.
- With reference to
FIG. 2 , the polymer is extruded through the spinneret or die 26 to formfilaments 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 byfinish applicator 4. Following the finish application and prior to the meter roll the filaments can be treated with turbulent air in theoptional preintermingling device 5 to even out the finish on the filaments. - The polymer is extruded through the spinneret or die at a temperature of at least about 200° C., preferably at least about 235° C., more preferably at least about 245° C., and up to about 275° C., preferably up to about 270° C., more preferably up to about 265° C.
- 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. As shown, 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 drawingrollers 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 thedrawing rollers 7. The filaments can then be cooled through acooling drum 9, and passed throughintermingler 11 viaroller 17, where the filaments are entangled. Thereafter, the filaments are wound with the use of a wind-upmachine 15 viaroller 13 and ayarn guide 16. - In accordance with the present invention, 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 disclosure of which is hereby incorporated herein by reference. - In the bulking unit described in U.S. Pat. No. 3,525,134, the filaments are both bulked and entangled. When other bulking units are used, 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.
- Using methods known in the art, the filaments can be ply-twisted and heat set into yarn. The yarn can then be made into carpet. Of course, other uses will readily occur to one of ordinary skill in the art having the benefit of the present disclosure. By way of example, the yarn of the present invention could also be used in rugs, woven tiles, automotive interiors and fabrics.
- Conditioning
- Poly(trimethylene terephthalate) (3GT) resins were dried at 120° C. for 50 hours under vacuum with a heated, dry nitrogen sweep using a VWR Model 1430M vacuum oven. The moisture level in the dried resins was measured at 180° C. with 10 minute delay time using a Mitsubishi Moisture Analyzer Model CA100 with a Vaporizer Model VA100. After drying, the moisture levels in the 3GT Sample 1 and
3GT Sample 2 were 38 and 40 ppm, respectively. - Procedures
- The melt stability and melt viscosity were measured at 250 and 260±0.1° C. using a Dynisco LCR 7002 capillary rheometer with a 1 mm diameter, 30:1 LID, 180° entrance angle die in accordance with test method ASTM D3835-02.
- The melt stability was measured following procedure 10.8.1 ASTM D3835-02. A constant rate test at 48.6 s−1 was used with a delay time of at least 1200 seconds. Extrudate samples were collected at 40, 120, 180, 250, 360, 600, 900, and 1200 seconds. The Goodyear IV of the as-received resins and extrudates were measured in 50/50 wt % trifluoroacetic acid/dichloromethane at 19° C. and a concentration of 0.4 g/dl using a Viscotek Forced Flow Viscometer Model Y-900, V5.7.
- The melt viscosity was measured following procedure 10.8.2. ASTM D3835-02. A multiple rate test with software detection of steady state (procedure X2) of ASTM D3835-02.was used with a melt time of 300 seconds and a shear rate of 48.6 s−1 repeated at the beginning, middle and end of each test. The melt viscosity stability was determined from the slope of the best-fit line through a plot of the repeated viscosity values versus dwell time (procedure X1.4) of ASTM D3835-02. The melt viscosity stability was used to correct the data at each shear rate to zero dwell time.
- Melt Stability
- Goodyear IV versus time from the extrudate samples is shown in Table 1. Both 3GT resins degrade with time at the test temperatures. The initial rapid loss up to ˜500 s is believed to be due to hydrolysis. At longer times (>500 s), the loss in IV is likely a result of thermal degradation. The rate of IV loss is about the same in both resins.
TABLE 1 3GT 3GT 3GT 3GT Time Sample 1 Sample 1 Sample 2Sample 2 (s) 250° C. 260° C. 250° C. 260° C. 0 1.031 1.031 0.936 0.936 40 1.016 1.014 0.928 0.926 120 1.006 1.000 0.927 0.897 180 1.004 0.985 0.914 0.897 250 0.987 0.980 0.895 0.879 360 0.980 0.960 0.884 0.858 600 0.963 0.932 0.874 0.849 900 0.943 0.908 0.854 0.827 1200 0.940 0.897 0.847 0.814
Melt Viscosity - Melt viscosity versus shear rate is shown in Table 2. The viscosity of the 3GT Sample 1 is higher compared to the
3GT Sample 2, consistent with a higher Goodyear IV.TABLE 2 Shear Rate 250° C. Avg CV 260° C. Avg CV (s−1) Test 1 Test 2Test 3 (Pa · s) (%) Test 1 Test 2Test 3 (Pa · s) (%) 3GT Sample 1 - Corrected Melt Viscosity 24.32 636.8 639.9 668.6 648.4 2.7 48.65 621.8 623.9 634.5 626.7 1.1 495.6 505.0 499.9 500.2 0.9 72.97 612.4 612.0 618.2 614.2 0.6 492.5 494.5 493.0 493.4 0.2 97.29 584.1 603.0 608.8 598.6 2.2 484.9 485.0 487.1 485.7 0.3 121.61 586.9 585.3 594.5 588.9 0.8 476.1 476.4 479.7 477.4 0.4 182.42 556.9 541.8 564.9 554.5 2.1 457.9 458.5 459.4 458.6 0.2 243.23 531.6 535.7 540.9 536.1 0.9 441.4 441.3 437.9 440.2 0.5 364.84 492.3 494.6 495.7 494.2 0.4 412.0 410.1 411.2 411.1 0.2 486.45 387.9 390.4 389.2 0.5 3GT Sample 2 - Corrected Melt Viscosity 24.32 314.8 317.3 308.5 313.6 1.4 258.4 247.3 273.8 259.8 5.1 48.65 308.9 309.1 317.4 311.8 1.6 251.8 243.7 262.1 252.5 3.0 72.97 298.1 300.6 299.4 0.6 241.2 241.5 260.2 247.6 3.6 97.29 300.2 300.1 303.8 301.4 0.7 247.2 238.4 258.8 248.1 3.4 121.61 297.1 294.6 306.9 299.5 2.2 247.1 234.6 255.9 245.9 3.5 182.42 242.9 230.9 250.6 241.5 3.3
Size Exclusion Chromatography Method to Measure Molecular Weight Distribution in Polymers Soluble in HFIP - Polymer samples were under dissolution for 2 hours in mobile phase solvent at 50° C. with moderate agitation (Automatic sample preparation system PL 260™ from Polymer Laboratories). All concentrations are in milligram per milliliter 20 (mg/ml). Mobile phase solvent was 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) with 0.01 molar sodium trifluoroacetate.
- Polymer solutions were injected into size exclusion chromatography system. The system included size exclusion chromatography system Model Alliance 2690™ from Waters Corporation (Milford, Mass.), with a Waters 410™ refractive index detector (Differential Refractive Index) and Viscotek Corporation (Houston, Tex.) Model T-60A™ dual detector module incorporating static right angle light scattering and differential capillary viscometer detectors. Columns for seperation were Two Shodex GPC HFIP-80M ™ styrene-divinyl benzene columns with exclusion limit 2×107 and 8,000/30 cm 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.
- Software used for data reduction was Trisec® Triple Detector SEC3 version 3.0 by Viscotek. Data reduction method was via triple detection method incorporating data from all three detectors: refractometer, viscometer and light scattering photometer (right angle). Flory-Fox equation is used for angular assymetry light scattering correction. No column calibration was involved in data processing. Sample concentration for 3GT polymers in HFIP was verified independently based on refractive index increment (dn/dc)=0.235. Number average molecular weight was calculated and reported as shown in Table 3.
TABLE 3 Number Average Molecular Weight Resin Measurement 1 Measurement 2Average 3GT Sample 1 33200 33200 33200 3GT Sample 226800 25300 26050 - Poly(trimethylene terephthalate)polymer (3GT, PTT) in chip form, specifically 3GT Sample 1, 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:
Zone 1 230° 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. In 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 (cm3/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/cm2. The spinnerets each had 68 trilobal (Y) holes with capillary diameter of 0.35×0.66 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 cm3/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.
- Textile measurements were:
Denier 1242 Tenacity, gm/den 2.63 Elongation, % 50 Modulus, gm/den 13.3 TYT, % TR 116. TYT, % CO2 14.5 TYT, % FS3 2.4
1TYT = Bulk measurement instrument of Lawson-Hemphill Electron Yarn Tester Model TYT-EW, % TR = Total Retraction
2% CO = Crimp Out
3% FS = Fiber Shrinkage
- Poly(trimethylene terephthalate)polymer (3GT, PTT) in chip form, specifically 3GTSample 1, 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:
Zone 1 230° 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 cm3/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/cm2. The spinnerets each have 68 trilobal (Y) holes with capillary diameter of 0.35×0.66 millimeters (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 0.25 meter per second (m/s). The filaments were pulled down through a one floor high interfloor tube (part of a 3 floor machine) to a Neumag spinning machine. At the bottom of the interfloor tube the two sets of 68 filaments were converged using finish applicators. The contact width of the upper applicators was 5 mm and the lower reversed finish applicators were 2 mm. Two 4 stream 0.8 cm3/rev finish pumps set at 40 rpm pumped P-7050T18 % Fiber Solutions finish to the finish applicators.
- The threadlines were led onto an inlet godet with a surface speed of 2390 m/min. Then, onto a metering godet duo set at 40° C. with a surface speed of 2400 m/min. The filaments were drawn in space with no assist by advancing to a set of enclosed heated duos set at 165° C. with a surface speed of 4100 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 7.5 bar and 225° C. impinged on the yarn bundles. The lamella exhaust cone had a vacuum setting of −95 m/bar. The textured or bulked yarn flowed out of the bottom of the chamber and piddled onto a cooling drum with a surface speed of 65 m/min.
- 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.
- Textile measurements were:
Denier 1212 Tenacity, gm/den 2.71 Elongation, % 51 Modulus, gm/den 13.1 TYT, % TR 16.4 TYT, % CO 13.8 TYT, % FS 3.0
1TYT = Bulk measurement instrument of Lawson-Hemphill Electron Yarn Tester Model TYT-EW, % TR = Total Retraction
2% CO = Crimp Out
3% FS = Fiber Shrinkage
Claims (42)
1. A process comprising:
(a) spinning molten poly(trimethylene terephthalate)polymer having a number average molecular weight of at least about 26500 and a melt viscosity of at least about 350 Pascals at 250° C. and 48.65 per second shear rate;
(b) converging the filaments into yarn;
(c) cooling the filaments; and
drawing the 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.
2. The process of claim 1 , wherein the number average molecular weight is from about 26500 to about 50000.
3. The process of claim 1 , wherein the number average molecular weight is from about 27500 to about 45000.
4. The process of claim 1 , wherein the number average molecular weight is from about 29000 to about 40000.
5. The process of claim 1 , wherein the melt viscosity is from about 350 to about 1000 Pascals at 250° C. and 48.65 per second shear rate.
6. The process of claim 1 , wherein the melt viscosity is from about 400 to about 900 Pascals at 250° C. and 48.65 per second shear rate.
7. The process of claim 1 , wherein the melt viscosity is from about 450 to about 800 Pascals at 250° C. and 48.65 per second shear rate.
8. The process of claim 1 , wherein the melt viscosity is from about 500 to about 700 Pascals at 250° C. and 48.65 per second shear rate.
9. The process of claim 1 , wherein the filament denier is at least 3.
10. The process of claim 1 , wherein the filament denier is at least 10.
11. The process of claim 1 , wherein the filament denier is at least 15.
12. The process of claim 1 , wherein the yarn denier is at least 250.
13. The process of claim 1 , wherein the yarn denier is at least 500.
14. The process of claim 1 , wherein the yarn denier is at least 1000.
15. The process of claim 1 , wherein the filaments are drawn at a speed of greater than 3500 meters per minute.
16. The process of claim 1 , wherein the filaments are drawn at a speed of greater than 4000 meters per minute.
17. The process of claim 1 , wherein the filaments are drawn at a speed of greater than 5000 meters per minute.
18. The process of claim 1 , wherein the filaments are drawn at a speed of at least 5100 meters per minute.
19. The process of claim 1 , wherein the filaments are drawn at a speed of at least 5500 meters per minute.
20. The process of claim 1 , further comprising coating the filaments with a spin finish and optionally preintermingling the filaments.
21. The process of claim 1 , further comprising bulking the drawn filaments.
22. The process of claim 21 , further comprising entangling the filaments.
23. The process of claim 21 , wherein the drawn filaments are bulked to form 3-dimensional curvilinear crimp therein.
24. The process of claim 23 , wherein the bulking comprises blowing and deforming the filaments in a hot-fluid jet bulking unit.
25. The process of claim 1 , wherein the filaments are drawn at a draw ratio of about 1.1 to about 4.0.
26. The process of claim 25 , wherein the draw ratio is about 1.2 to about 3.0.
27. The process of claim 25 , wherein the draw ratio is about 1.4 to about 2.2.
28. The process of claim 1 , wherein the poly(trimethylene terephthalate) has an intrinsic viscosity of about 0.95 to about 1.10.
29. The process of claim 28 , wherein the intrinsic viscosity is about 0.98 to about 1.04.
30. The process of claim 28 , wherein the intrinsic viscosity is about 1.00 to about 1.02.
31. A process comprising:
(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 denier greater than 1 and yarn having a yarn denier greater than 210;
(g) bulking the drawn filaments such that the filaments are blown and deformed in three dimensions with a hot bulking fluid to form bulked continuous filaments having random 3-dimensional curvilinear crimp;
(h) cooling the bulked continuous filaments to a temperature less than the glass transition temperature of the polymer filaments; and
(i) entangling the bulked continuous filaments.
32. The process of claim 31 , wherein the water content is less than about 50 ppm.
33. The process of claim 31 , wherein the water content is less than about 40 ppm.
34. The process of claim 31 , wherein the bulked continuous filaments of (g) are entangled before the cooling in (h).
35. The process of claim 31 , wherein the filaments are drawn at a speed of at least 3000 meters per minute.
36. The process of claim 31 , wherein the filaments are drawn at a speed of greater than about 3500 meters per minute.
37. The process of claim 31 , wherein the filaments are drawn at a speed of at least about 4000 meters per minute.
38. The process of claim 31 , wherein the filaments are drawn at a speed of at least 5000 meters per minute.
39. The process of claim 31 , wherein the filaments are drawn at a speed of at least 5100 meters per minute.
40. The process of claim 31 , wherein the filaments are drawn at a speed of at least 5500 meters per minute.
41. The process of claim 31 , further comprising ply-twisting and heat setting the filaments into yarn.
42. Carpet made from the ply-twisted, heat-set poly(trimethylene terephthalate) yarn of claim 41.
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/752,399 US20050147784A1 (en) | 2004-01-06 | 2004-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
PCT/US2005/000774 WO2005068695A1 (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
CA002552662A CA2552662A1 (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
EP05711340A EP1702092A4 (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
CN200580001824XA CN1906340B (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene 1,3-terephthalate) fiber |
KR1020067013476A KR20060123432A (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
MXPA06007683A MXPA06007683A (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene terephthalate) fiber. |
TW094100397A TW200602525A (en) | 2004-01-06 | 2005-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
JP2006549507A JP2007521422A (en) | 2004-01-06 | 2005-01-06 | Method for producing poly (trimethylene terephthalate) fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/752,399 US20050147784A1 (en) | 2004-01-06 | 2004-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
US20050147784A1 true US20050147784A1 (en) | 2005-07-07 |
Family
ID=34711624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/752,399 Abandoned US20050147784A1 (en) | 2004-01-06 | 2004-01-06 | Process for preparing poly(trimethylene terephthalate) fiber |
Country Status (9)
Country | Link |
---|---|
US (1) | US20050147784A1 (en) |
EP (1) | EP1702092A4 (en) |
JP (1) | JP2007521422A (en) |
KR (1) | KR20060123432A (en) |
CN (1) | CN1906340B (en) |
CA (1) | CA2552662A1 (en) |
MX (1) | MXPA06007683A (en) |
TW (1) | TW200602525A (en) |
WO (1) | WO2005068695A1 (en) |
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---|---|---|---|---|
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Citations (64)
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 |
US5645782A (en) * | 1994-06-30 | 1997-07-08 | E. I. Du Pont De Nemours And Company | Process for making poly(trimethylene terephthalate) bulked continuous filaments |
US5798433A (en) * | 1997-02-12 | 1998-08-25 | Zimmer Aktiengesellschaft | Process for production of polypropylene terephthalate |
US5804115A (en) * | 1996-12-13 | 1998-09-08 | Basf Corporation | One step, ready-to-tuft, mock space-dyed multifilament yarn |
US5840957A (en) * | 1998-03-16 | 1998-11-24 | E. I. Du Pont De Nemours And Company | Transesterification process using lanthanum compound catalyst |
US5994451A (en) * | 1998-04-24 | 1999-11-30 | Shell Oil Company | Polytrimethylene terephthalate composition |
US6093786A (en) * | 1996-11-27 | 2000-07-25 | Shell Oil Company | Process for preparing polytrimethylene terephthalate |
US6109015A (en) * | 1998-04-09 | 2000-08-29 | Prisma Fibers, Inc. | Process for making poly(trimethylene terephthalate) yarn |
US6113825A (en) * | 1995-05-08 | 2000-09-05 | Shell Oil Company | Process for preparing poly(trimethylene terephthalate) carpet yarn |
US6218008B1 (en) * | 2000-07-21 | 2001-04-17 | Hyosung Corporation | Easy dyeable polyester fiber |
US6242558B1 (en) * | 1996-11-27 | 2001-06-05 | Shell Oil Company | Modified polytrimethylene terephthalate |
US6254961B1 (en) * | 1995-05-08 | 2001-07-03 | Shell Oil Company | Process for preparing poly(trimethylene terephthalate) carpet yarn |
US6255442B1 (en) * | 2000-02-08 | 2001-07-03 | E. I. Du Pont De Nemours And Company | Esterification process |
US6277947B1 (en) * | 2000-04-21 | 2001-08-21 | Shell Oil Company | Process of producing polytrimethylene terephthalate (PTT) |
US6281325B1 (en) * | 1999-08-25 | 2001-08-28 | E. I. Du Pont De Nemours And Company | Preparation of poly(trimethylene terephthalate) |
US6284370B1 (en) * | 1997-11-26 | 2001-09-04 | Asahi Kasei Kabushiki Kaisha | Polyester fiber with excellent processability and process for producing the same |
US6287688B1 (en) * | 2000-03-03 | 2001-09-11 | E. I. Du Pont De Nemours And Company | Partially oriented poly(trimethylene terephthalate) yarn |
US6297315B1 (en) * | 1999-05-11 | 2001-10-02 | Shell Oil Company | Process for preparing polytrimethylene terephthalate |
US6315934B1 (en) * | 1995-05-08 | 2001-11-13 | Shell Oil Company | Process for preparing poly(thimethylene therephthalate) carpet yarn |
US6316101B2 (en) * | 1997-09-03 | 2001-11-13 | Asahi Kasei Kogyo Kabushiki Kaisha | Polyester fiber and fabrics made by using the same |
US6331264B1 (en) * | 1999-03-31 | 2001-12-18 | E. I. Du Pont De Nemours And Company | Low emission polymer compositions |
US6350895B1 (en) * | 1999-03-26 | 2002-02-26 | E. I. Du Pont De Nemours And Company | Transesterification process using yttrium and samarium compound catalystis |
US6353062B1 (en) * | 2000-02-11 | 2002-03-05 | E. I. Du Pont De Nemours And Company | Continuous process for producing poly(trimethylene terephthalate) |
US6383632B2 (en) * | 2000-03-03 | 2002-05-07 | E. I. Du Pont De Nemours And Company | Fine denier yarn from poly (trimethylene terephthalate) |
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 |
US6423407B1 (en) * | 1998-10-15 | 2002-07-23 | Asahi Kasei Kabushiki Kaisha | Polytrimethylene terephthalate fiber |
US6441129B2 (en) * | 2000-05-02 | 2002-08-27 | Shell Oil Company | High temperature solid state polymerization of poly (trimethylene terephthalate) |
US20020116802A1 (en) * | 2000-07-14 | 2002-08-29 | Marc Moerman | Soft and stretchable textile fabrics made from polytrimethylene terephthalate |
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 |
US20020130437A1 (en) * | 2000-11-03 | 2002-09-19 | Dietmar Wandel | Method of spinning, spooling, and stretch texturing Polyester filaments and polyesters thereby produced |
US20020147298A1 (en) * | 1999-11-12 | 2002-10-10 | Yanhui Sun | Polyamide compounds |
US6495254B1 (en) * | 1999-03-15 | 2002-12-17 | Asahi Kasei Kabushiki Kaisha | Poly(trimethylene terephthalate) fiber |
US20020197444A1 (en) * | 2001-05-14 | 2002-12-26 | Lee Kyool Seop | Method for preparing poly (trimethylene terephthalate) carpet |
US20030004301A1 (en) * | 2000-11-03 | 2003-01-02 | Dietmar Wandel | Method of spinning, spooling, and stretch texturing polyester filaments and polyester filaments thereby produced |
US6509438B2 (en) * | 2000-04-21 | 2003-01-21 | Shell Oil Company | Optimum dipropylene glycol content polytrimethylene terephthalate compositions |
US6512080B2 (en) * | 1999-04-22 | 2003-01-28 | Shell Oil Company | Process of producing polytrimethylene terephthalate (PTT) |
US20030035949A1 (en) * | 2000-04-04 | 2003-02-20 | Masao Uchida | Polyester fiber for false twisting |
US6528579B2 (en) * | 2000-02-17 | 2003-03-04 | Shell Oil Company | Zero-heel polyester process |
US20030045611A1 (en) * | 2001-06-29 | 2003-03-06 | Agarwal Nirmal K. | Process for preparing pigmented shaped articles comprising poly (trimethylene terephthalate) |
US6538076B2 (en) * | 2000-02-11 | 2003-03-25 | E. I. Du Pont De Nemours And Company | Continuous process for producing poly(trimethylene terephthalate) |
US20030064219A1 (en) * | 2001-05-14 | 2003-04-03 | Lee Kyool Seop | Poly (trimethylene terephthalate) BCF carpet yarn with noncircular cross section and method for preparing the same |
US6572967B1 (en) * | 1999-09-30 | 2003-06-03 | Asahi Kasei Kabushiki Kaisha | Poly(trimethylene terephthalate) multifilament yarn |
US20030111171A1 (en) * | 2002-09-09 | 2003-06-19 | Casey Paul Karol | Poly(trimethylene) terephthalate texile staple production |
US6610819B2 (en) * | 2001-06-01 | 2003-08-26 | Shell Oil Company | Reduction of friability of poly(trimethylene terephthalate) |
US20030160351A1 (en) * | 2002-02-20 | 2003-08-28 | Kailash Dangayach | Process for making stable polytrimethylene terephthalate packages |
US6620502B1 (en) * | 1999-07-12 | 2003-09-16 | Asahi Kasei Kabushiki Kaisha | Polytrimethylene terephthalate fiber and process for producing the same |
US20030180533A1 (en) * | 2000-05-12 | 2003-09-25 | Tadashi Koyanagi | Pre-oriented yarn package |
US6652964B1 (en) * | 1997-08-18 | 2003-11-25 | Asahi Kasei Kabushiki Kaisha | Polyester fiber and fabric prepared therefrom |
US6656583B1 (en) * | 1999-08-10 | 2003-12-02 | Lurgi Zimmer Ag | High-strength polyester threads and method for producing the same |
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 |
US6667096B2 (en) * | 2000-11-03 | 2003-12-23 | Zimmer A.G. | Method of spinning, spooling, and stretch texturing polyester filaments and polyester filaments produced |
US6680353B1 (en) * | 1998-10-30 | 2004-01-20 | Asahi Kasei Kabushiki Kaisha | Polyester resin composition and fiber |
US6685859B2 (en) * | 2000-03-03 | 2004-02-03 | E. I. Du Pont De Nemours And Company | Processes for making poly(trimethylene terephthalate) yarn |
US6702864B2 (en) * | 2000-10-11 | 2004-03-09 | Shell Oil Company | Process for making high stretch and elastic knitted fabrics from polytrimethylene terephthalate |
US6709689B2 (en) * | 2000-07-06 | 2004-03-23 | Asahi Kasei Kabushiki Kaisha | Drawn yarn package and production method therefor |
US6740733B2 (en) * | 2001-11-30 | 2004-05-25 | Shell Oil Company | Process and apparatus for crystallization of polytrimethylene terephthalate (PTT) |
US6740400B2 (en) * | 2001-02-07 | 2004-05-25 | Asahi Kasei Kabushiki Kaisha | Poly (trimethylene terephthalate) and a process for producing the same |
US6752945B2 (en) * | 2000-09-12 | 2004-06-22 | E. I. Du Pont De Nemours And Company | Process for making poly(trimethylene terephthalate) staple fibers |
US6777059B2 (en) * | 2002-03-13 | 2004-08-17 | E.I. Du Pont De Nemours And Company | Treated poly(trimethylene terephthalate) carpets |
US20040186264A1 (en) * | 2001-05-25 | 2004-09-23 | Randolf Reimann | Method and device for the production of polytrimethylene terephthalate |
US6800718B1 (en) * | 1999-04-22 | 2004-10-05 | Zimmer Aktiengesellschaft | Process for producing polytrimethylene terephthalate (PTT) |
US6916535B2 (en) * | 2001-10-11 | 2005-07-12 | Asahi Kasei Kabushiki Kaisha | Poly (trimethylene terephthalate) pellets and method for production thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19934551A1 (en) * | 1999-07-22 | 2001-01-25 | Lurgi Zimmer Ag | Polytrimethyleneterephthalate staple fibers for textile, especially carpet manufacture, have specific properties and can be dyed with dispersion colors without addition of a carrier |
JP3862996B2 (en) * | 2001-10-31 | 2006-12-27 | 帝人ファイバー株式会社 | Polytrimethylene terephthalate filament yarn and method for producing the same |
-
2004
- 2004-01-06 US US10/752,399 patent/US20050147784A1/en not_active Abandoned
-
2005
- 2005-01-06 EP EP05711340A patent/EP1702092A4/en not_active Withdrawn
- 2005-01-06 WO PCT/US2005/000774 patent/WO2005068695A1/en not_active Application Discontinuation
- 2005-01-06 TW TW094100397A patent/TW200602525A/en unknown
- 2005-01-06 KR KR1020067013476A patent/KR20060123432A/en not_active Application Discontinuation
- 2005-01-06 CA CA002552662A patent/CA2552662A1/en not_active Abandoned
- 2005-01-06 JP JP2006549507A patent/JP2007521422A/en not_active Abandoned
- 2005-01-06 CN CN200580001824XA patent/CN1906340B/en not_active Expired - Fee Related
- 2005-01-06 MX MXPA06007683A patent/MXPA06007683A/en unknown
Patent Citations (73)
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 |
US5645782A (en) * | 1994-06-30 | 1997-07-08 | E. I. Du Pont De Nemours And Company | Process for making poly(trimethylene terephthalate) bulked continuous filaments |
US5662980A (en) * | 1994-06-30 | 1997-09-02 | E.I. Du Pont De Nemours And Company | Carpets made from poly(trimethylene terephthalate) bulked continuous filaments |
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 |
US6254961B1 (en) * | 1995-05-08 | 2001-07-03 | Shell Oil Company | Process for preparing poly(trimethylene terephthalate) carpet yarn |
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 |
US5798433A (en) * | 1997-02-12 | 1998-08-25 | Zimmer Aktiengesellschaft | Process for production of polypropylene terephthalate |
US6652964B1 (en) * | 1997-08-18 | 2003-11-25 | Asahi Kasei Kabushiki Kaisha | Polyester fiber and fabric prepared therefrom |
US6423814B1 (en) * | 1997-09-03 | 2002-07-23 | Asahi Kasei Kabushiki Kaisha | Polyester resin composition |
US6316101B2 (en) * | 1997-09-03 | 2001-11-13 | Asahi Kasei Kogyo Kabushiki Kaisha | Polyester fiber and fabrics made by using the same |
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 |
US6423407B1 (en) * | 1998-10-15 | 2002-07-23 | Asahi Kasei Kabushiki Kaisha | Polytrimethylene terephthalate fiber |
US6680353B1 (en) * | 1998-10-30 | 2004-01-20 | Asahi Kasei Kabushiki Kaisha | Polyester resin composition and fiber |
US6495254B1 (en) * | 1999-03-15 | 2002-12-17 | Asahi Kasei Kabushiki Kaisha | Poly(trimethylene terephthalate) fiber |
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 |
US6800718B1 (en) * | 1999-04-22 | 2004-10-05 | Zimmer Aktiengesellschaft | Process for producing polytrimethylene terephthalate (PTT) |
US6326456B2 (en) * | 1999-04-22 | 2001-12-04 | Shell Oil Company | Process of producing polytrimethylene terephthalate (PTT) |
US6512080B2 (en) * | 1999-04-22 | 2003-01-28 | 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 |
US6620502B1 (en) * | 1999-07-12 | 2003-09-16 | Asahi Kasei Kabushiki Kaisha | Polytrimethylene terephthalate fiber and process for producing the same |
US6656583B1 (en) * | 1999-08-10 | 2003-12-02 | Lurgi Zimmer Ag | High-strength polyester threads and method for producing the same |
US6281325B1 (en) * | 1999-08-25 | 2001-08-28 | E. I. Du Pont De Nemours And Company | Preparation of poly(trimethylene terephthalate) |
US6335421B1 (en) * | 1999-08-25 | 2002-01-01 | E. I. Du Pont De Nemours And Company | Preparation of poly(trimethylene terephthalate) with low level of di(1,3-propylene glycol) |
US6572967B1 (en) * | 1999-09-30 | 2003-06-03 | Asahi Kasei Kabushiki Kaisha | Poly(trimethylene terephthalate) multifilament yarn |
US20020147298A1 (en) * | 1999-11-12 | 2002-10-10 | Yanhui Sun | Polyamide compounds |
US6255442B1 (en) * | 2000-02-08 | 2001-07-03 | E. I. Du Pont De Nemours And Company | Esterification process |
US6426398B2 (en) * | 2000-02-08 | 2002-07-30 | E. I. Du Pont De Nemours And Company | Poly (trimethylene terephthalate) polymer composition |
US6538076B2 (en) * | 2000-02-11 | 2003-03-25 | 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 |
US6685859B2 (en) * | 2000-03-03 | 2004-02-03 | E. I. Du Pont De Nemours And Company | Processes for making poly(trimethylene terephthalate) yarn |
US6287688B1 (en) * | 2000-03-03 | 2001-09-11 | E. I. Du Pont De Nemours And Company | Partially oriented poly(trimethylene terephthalate) yarn |
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US6610819B2 (en) * | 2001-06-01 | 2003-08-26 | Shell Oil Company | Reduction of friability of poly(trimethylene terephthalate) |
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Also Published As
Publication number | Publication date |
---|---|
CN1906340A (en) | 2007-01-31 |
EP1702092A4 (en) | 2007-12-05 |
TW200602525A (en) | 2006-01-16 |
WO2005068695A1 (en) | 2005-07-28 |
KR20060123432A (en) | 2006-12-01 |
JP2007521422A (en) | 2007-08-02 |
CN1906340B (en) | 2012-07-04 |
CA2552662A1 (en) | 2005-07-28 |
EP1702092A1 (en) | 2006-09-20 |
MXPA06007683A (en) | 2006-09-01 |
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