[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

EP0494432A2 - Melt-colored thick and thin yarn - Google Patents

Melt-colored thick and thin yarn Download PDF

Info

Publication number
EP0494432A2
EP0494432A2 EP91122036A EP91122036A EP0494432A2 EP 0494432 A2 EP0494432 A2 EP 0494432A2 EP 91122036 A EP91122036 A EP 91122036A EP 91122036 A EP91122036 A EP 91122036A EP 0494432 A2 EP0494432 A2 EP 0494432A2
Authority
EP
European Patent Office
Prior art keywords
melt
process according
yarn
colored
poly
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP91122036A
Other languages
German (de)
French (fr)
Other versions
EP0494432A3 (en
Inventor
Stuart H. Rice, Jr.
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Corp
Original Assignee
BASF Corp
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 BASF Corp filed Critical BASF Corp
Publication of EP0494432A2 publication Critical patent/EP0494432A2/en
Publication of EP0494432A3 publication Critical patent/EP0494432A3/en
Withdrawn legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/20Formation of filaments, threads, or the like with varying denier along their length
    • 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
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/04Pigments
    • 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

Definitions

  • the present invention relates to melt-colored synthetic polymer yarn containing fibers or filaments having a random distribution of light and dark sections. More particularly, it relates to fibers or filaments of this type which are produced without dyeing and which correspond to denier fluctuations or variations of random size in the direction of the axis of the fibers or filaments. It also relates to yarns made therefrom, and a method of preparing such yarns.
  • Man-made fibers are generally produced by spining and drawing. In most instances, the fibers produced by this procedure are substantially uniform in thickness. However, in certain applications, it is important that yarns contain filaments having a variable denier. For instance, such yarns are useful in providing the means of producing variable texture in fabrics made therefrom and the fabrics containing such yarns have an attractive appearance, i.e., a "busy" looking fabric, and a pleasing feel to the touch.
  • variable denier fabrics may be dyed, thus producing mottled or other novelty effects owing to the varying rates and extent to which the dyestuff is taken up by the portions of different denier. While these conventionally dyed thick and thin yarns are currently in high demand, the added step of dyeing after the initial spinning and drawing of these variable denier yarns creates an extra step in the production process and an increased cost factor. Additionally, the problem of dye lightfastness of the fabric becomes a concern when the dye is applied at a post spinning and drawing stage. While fabrics prepared in this manner may be suitable for wearing apparel, they are less suitable as automotive fabrics, upholstery, curtain fabrics and the like.
  • variable denier synthetic polymer fibers, filaments, and fabrics made therefrom exhibiting improved dye lightfastness without the need to be dyed.
  • the present invention provides a process for producing a variable denier melt-colored synthetic polymeric filamentous yarn, having a random distribution of light and dark sections, produced without dyeing and exhibiting improved dye lightfastness, which comprises creating a melt-colored polymer mixture, spinning a melt-colored yarn from said synthetic melt-colored polymer mixture, and subjecting said melt-colored synthetic yarn to a thick and thin drawing process so as to produce a filamentous yarn of variable denier.
  • Preferred synthetic polymers include linear terephthalate polyesters (PET), those being polyesters of glycol containing from 2 to 20 carbon atoms and a dicarboxylic acid compound comprising at least about 75% terephthalatic acid. The remainder, if any, of the dicarboxylic acid compound may be any suitable dicarboxylic acid.
  • the preferred polyester is poly(ethyleneterephthalate).
  • the feeder yarn utilized to prepare the yarn and filaments of the present invention will have a birefringence in the range of about 0.01 to about 0.05.
  • the preferred melt coloring agent is a colored pigment in a polyethylene carrier.
  • the most preferred melt coloring agent is a colored agent in a PET carrier.
  • fiber as used herein includes fibers of extreme or indefinite length (i.e., filaments) and fibers of short length (i.e., staple).
  • fibers of extreme or indefinite length i.e., filaments
  • fibers of short length i.e., staple
  • bond as used herein means a continuous strand of fibers.
  • fabric as used herein includes a textile structure composed of mechanically interlocked fibers or filaments.
  • the structure can be nonwoven, woven or knitted.
  • multifilament yarn as used herein means a yarn comprised of a plurality of individual filaments or strands.
  • glass transition temperature means the temperature at which an amorphous polymer or the amorphous regions of a partially crystalline polymer changes to or from a hard and relatively brittle state to a more flexible or rubbery condition. At sufficiently low temperatures, all amorphous polymers or amorphous regions of semicrystalline polymers assume characteristics of glasses, such as hardness, stiffness, and brittleness. Polymers in the glassy state are characterized by a low volume coefficient of expansion, when compared with that of the polymer in the fluid state. In this respect, polymers in the glassy state resemble crystalline polymers which are also characterized by a low volume coefficient of expansion. The temperature interval at which the volume coefficient of expansion of the amorphous polymer changes from a high to a low value is the glass transition temperature range.
  • Birefringence ( ⁇ n) is obtained in the following manner: Sodium D rays (wavelength 589 millimicrons) are used as a light source, and the filaments are disposed in a diagonal position
  • the birefringence ( ⁇ n) of the specimen is computed from the following equation: when n is the interference fringe due to the degree of orientation of the polymer molecular chain; r is the retardation obtained by measuring the orientation not developing into the interference fringe by means of a Berek's compensator; a is the diameter of the filament; and ⁇ is the wavelength of the sodium D rays.
  • Fiber-forming synthetic polymers suitable for use in the present invention include synthetic polymers having a glass transition temperature (T g ) of at least 30°C.
  • Preferred synthetic polymers include linear terephthalate polyesters (PET), i.e., polyesters of a glycol containing from 2 to 20 carbon atoms and a dicarboxylic acid component comprising at least about 75% terephthalic acid.
  • PET linear terephthalate polyesters
  • the remainder, if any, of the dicarboxylic acid component may be any suitable dicarboxylic acid such as sebacic acid, adipic acid, isophthalic acid, sulfonyl-4,4-dibenzoic acid, or 2,8-dibenzofurandicarboxylic acid.
  • linear terephthalate polyesters which may be employed include poly(ethyleneterephthalate), poly(butylene terephthalate), poly(ethyleneterephthalate/5-chloroisophthalate)(85/15), poly(ethyleneterephthalate/5-[sodium sulfo] isophthalate)(97/3), or poly(cyclohexane-1,4dimethyleneterephthalate/hexahydroterephthalate) (75/25).
  • the preferred polyester is poly(ethylene terephthalate), which includes a linear polyester in which at least about 85% of the recurring structural units are ethylene terephthalate units of the following formula:
  • the linear polyester contains at least ninety percent (90%) recurring structural units of ethylene terephthalate.
  • the polyester is substantially all poly(ethylene terephthalate). Up to 15 mole percent of other copolymerizable ester units other than poly(ethylene terephthalate) can also be present.
  • the feeder yarn utilized to prepare the yarn and filaments of the present invention must have sufficient molecular orientation (birefringence- n).
  • the amount of birefringence in the feeder yarn will be an amount in the range of from about 0.01 to about 0.05, and, more preferably, from about 0.015 to 0.031, and, most preferably, about 0.018.
  • the take-up speed will generally be in the range of from about 1,600 to about 4,000 meters/minute, preferably, from about 1,800 to about 2,800 meters/minute, and most preferably, about 2,000 meters/minute.
  • the feeder yarn should be aged for a sufficient amount of time, typically about 24 hours to about 7 days.
  • variable denier filaments of the present invention are prepared by drawing, at ambient temperature, i.e., 15°-30°C, the feeder yarn having the above described molecular orientation (birefringence) at a draw ratio of from about 1.27 to about 2.07 and in a draw zone having a length of from about 15.2 to about 300 cm. More preferably, the draw ratio is from about 1.69 to about 1.97 and the draw zone has a length of from about 30.5 to about 81.3 cm. Most preferably, the draw ratio is about 1.97 and the length of the draw zone is 61 cm.
  • the resulting thick and thin filaments contain slubs which preferably have a length in the range of from about 1.4 inches to 30.9 inches, an average length of slub of from about 9.1 to about 16.2 inches, and occupy from about 16.4 to about 49.8 percent of the longitudinal axis of the filaments.
  • the above-recited percent of occupancy, length of slub, and average length of slub are obtained by measuring 50 feet of at least 10 filaments which have been selected at random.
  • Melt-coloring agents suitable for use in the present invention are inorganic and organic pigments in a thermoplastic earner.
  • This carrier can be PET, nylon, polyethylene or any other carrier suitable for pigment dispersion. Examples are carbon black pigment in a PET carrier and navy blue pigment in a PET carrier.
  • the preferred melt coloring agent is a colored pigment in a polyethylene carrier.
  • the most preferred melt coloring agent is a colored pigment in a PET carrier.
  • the yarns comprising the variable denier filaments can be processed into fabrics which find particular use in draperies, upholstery fabrics, and automotive upholstery applications.
  • a PET yarn was produced by melt spinning molten PET and winding up the yarn at different winding speeds ranging from 1600 to 2725 mpm. Carbon black pigment in a concentration range up to 0.25 wt. percent was added to the molten PET prior to spinning. The feeder yarns were then drawn at ambient temperature, using a draw ratio range of 1.69 to 2.07, and a draw zone of 24 inches. Test Sample Winding Speed (mpm) Birefringence Pigment (wt.
  • the yarns produced at these conditions had a random distribution of light and dark sections without the necessity of dyeing, and showed improved dye lightfastness.
  • a PET yarn was produced by melt spinning molten PET with 0.20 wt. percent navy pigment added to the molten PET prior to spinning. This yarn was wound at 1600 mpm and drawn at ambient temperature at a draw ratio of 2.02 and a draw zone of 24 inches.
  • Test Sample Winding Speed (mpm) Birefringence Pigment (wt. %) 1 1600 0.014 0.10 2 1600 0.014 0.20 3 1600 0.014 0.25
  • a yarn with random dark blue and light blue sections was produced, without dyeing, and showing improved dye lightfastness.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Artificial Filaments (AREA)

Abstract

The present invention provides a process for producing a variable denier melt-colored synthetic polymeric filamentous yarn, having a random distribution of light and dark sections, produced without dyeing and exhibiting improved dye lightfastness, which comprises creating a melt-colored polymer mixture, spinning a melt-colored yarn from said synthetic melt-colored polymer mixture, and subjecting said melt-colored synthetic yarn to a thick and thin drawing process to produce a filamentous yarn of variable denier.

Description

    Field of the Invention
  • The present invention relates to melt-colored synthetic polymer yarn containing fibers or filaments having a random distribution of light and dark sections. More particularly, it relates to fibers or filaments of this type which are produced without dyeing and which correspond to denier fluctuations or variations of random size in the direction of the axis of the fibers or filaments. It also relates to yarns made therefrom, and a method of preparing such yarns.
  • Background of the Invention
  • Man-made fibers are generally produced by spining and drawing. In most instances, the fibers produced by this procedure are substantially uniform in thickness. However, in certain applications, it is important that yarns contain filaments having a variable denier. For instance, such yarns are useful in providing the means of producing variable texture in fabrics made therefrom and the fabrics containing such yarns have an attractive appearance, i.e., a "busy" looking fabric, and a pleasing feel to the touch.
  • It is known in the art that these variable denier fabrics may be dyed, thus producing mottled or other novelty effects owing to the varying rates and extent to which the dyestuff is taken up by the portions of different denier. While these conventionally dyed thick and thin yarns are currently in high demand, the added step of dyeing after the initial spinning and drawing of these variable denier yarns creates an extra step in the production process and an increased cost factor. Additionally, the problem of dye lightfastness of the fabric becomes a concern when the dye is applied at a post spinning and drawing stage. While fabrics prepared in this manner may be suitable for wearing apparel, they are less suitable as automotive fabrics, upholstery, curtain fabrics and the like.
  • Therefore, a need exists in the art for a method to produce these variable denier synthetic polymer fibers, filaments, and fabrics made therefrom, exhibiting improved dye lightfastness without the need to be dyed.
  • Summary of the Invention
  • The present invention provides a process for producing a variable denier melt-colored synthetic polymeric filamentous yarn, having a random distribution of light and dark sections, produced without dyeing and exhibiting improved dye lightfastness, which comprises creating a melt-colored polymer mixture, spinning a melt-colored yarn from said synthetic melt-colored polymer mixture, and subjecting said melt-colored synthetic yarn to a thick and thin drawing process so as to produce a filamentous yarn of variable denier.
  • Preferred synthetic polymers include linear terephthalate polyesters (PET), those being polyesters of glycol containing from 2 to 20 carbon atoms and a dicarboxylic acid compound comprising at least about 75% terephthalatic acid. The remainder, if any, of the dicarboxylic acid compound may be any suitable dicarboxylic acid. The preferred polyester is poly(ethyleneterephthalate). The feeder yarn utilized to prepare the yarn and filaments of the present invention will have a birefringence in the range of about 0.01 to about 0.05. The preferred melt coloring agent is a colored pigment in a polyethylene carrier. The most preferred melt coloring agent is a colored agent in a PET carrier.
  • Definitions
  • The term "fiber" as used herein includes fibers of extreme or indefinite length (i.e., filaments) and fibers of short length (i.e., staple). The term "yarn" as used herein means a continuous strand of fibers.
  • The term "fabric" as used herein includes a textile structure composed of mechanically interlocked fibers or filaments. The structure can be nonwoven, woven or knitted.
  • The term "multifilament yarn" as used herein means a yarn comprised of a plurality of individual filaments or strands.
  • The term "glass transition temperature" (Tg) means the temperature at which an amorphous polymer or the amorphous regions of a partially crystalline polymer changes to or from a hard and relatively brittle state to a more flexible or rubbery condition. At sufficiently low temperatures, all amorphous polymers or amorphous regions of semicrystalline polymers assume characteristics of glasses, such as hardness, stiffness, and brittleness. Polymers in the glassy state are characterized by a low volume coefficient of expansion, when compared with that of the polymer in the fluid state. In this respect, polymers in the glassy state resemble crystalline polymers which are also characterized by a low volume coefficient of expansion. The temperature interval at which the volume coefficient of expansion of the amorphous polymer changes from a high to a low value is the glass transition temperature range.
  • Birefringence (Δ n) is obtained in the following manner:
       Sodium D rays (wavelength 589 millimicrons) are used as a light source, and the filaments are disposed in a diagonal position The birefringence (Δ n) of the specimen is computed from the following equation:
    Figure imgb0001

    when n is the interference fringe due to the degree of orientation of the polymer molecular chain; r is the retardation obtained by measuring the orientation not developing into the interference fringe by means of a Berek's compensator; a is the diameter of the filament; and λ is the wavelength of the sodium D rays.
  • Detailed Description of the Preferred Embodiments
  • A number of procedures are known in the art for producing filaments having a variable denier. One such method, for example, is that of Stanko et al. U. S. Patent No. 4,906,519. Fiber-forming synthetic polymers suitable for use in the present invention include synthetic polymers having a glass transition temperature (Tg) of at least 30°C.
  • Preferred synthetic polymers include linear terephthalate polyesters (PET), i.e., polyesters of a glycol containing from 2 to 20 carbon atoms and a dicarboxylic acid component comprising at least about 75% terephthalic acid. The remainder, if any, of the dicarboxylic acid component may be any suitable dicarboxylic acid such as
    sebacic acid,
    adipic acid,
    isophthalic acid,
    sulfonyl-4,4-dibenzoic acid, or
    2,8-dibenzofurandicarboxylic acid.
  • Examples of linear terephthalate polyesters which may be employed include
    poly(ethyleneterephthalate),
    poly(butylene terephthalate),
    poly(ethyleneterephthalate/5-chloroisophthalate)(85/15),
    poly(ethyleneterephthalate/5-[sodium sulfo] isophthalate)(97/3), or
    poly(cyclohexane-1,4dimethyleneterephthalate/hexahydroterephthalate) (75/25).
  • The preferred polyester is poly(ethylene terephthalate), which includes a linear polyester in which at least about 85% of the recurring structural units are ethylene terephthalate units of the following formula:
    Figure imgb0002
  • More preferably, the linear polyester contains at least ninety percent (90%) recurring structural units of ethylene terephthalate. In a particularly preferred embodiment of the process, the polyester is substantially all poly(ethylene terephthalate). Up to 15 mole percent of other copolymerizable ester units other than poly(ethylene terephthalate) can also be present.
  • The feeder yarn utilized to prepare the yarn and filaments of the present invention must have sufficient molecular orientation (birefringence- n). The amount of birefringence in the feeder yarn will be an amount in the range of from about 0.01 to about 0.05, and, more preferably, from about 0.015 to 0.031, and, most preferably, about 0.018.
  • In order for the feeder yarn to have sufficient molecular orientation, the take-up speed will generally be in the range of from about 1,600 to about 4,000 meters/minute, preferably, from about 1,800 to about 2,800 meters/minute, and most preferably, about 2,000 meters/minute.
  • In order to achieve maximum contrast between the thick and thin sections of the yarn, the feeder yarn should be aged for a sufficient amount of time, typically about 24 hours to about 7 days.
  • The variable denier filaments of the present invention are prepared by drawing, at ambient temperature, i.e., 15°-30°C, the feeder yarn having the above described molecular orientation (birefringence) at a draw ratio of from about 1.27 to about 2.07 and in a draw zone having a length of from about 15.2 to about 300 cm. More preferably, the draw ratio is from about 1.69 to about 1.97 and the draw zone has a length of from about 30.5 to about 81.3 cm. Most preferably, the draw ratio is about 1.97 and the length of the draw zone is 61 cm.
  • The resulting thick and thin filaments contain slubs which preferably have a length in the range of from about 1.4 inches to 30.9 inches, an average length of slub of from about 9.1 to about 16.2 inches, and occupy from about 16.4 to about 49.8 percent of the longitudinal axis of the filaments. The above-recited percent of occupancy, length of slub, and average length of slub are obtained by measuring 50 feet of at least 10 filaments which have been selected at random.
  • Melt-coloring agents suitable for use in the present invention are inorganic and organic pigments in a thermoplastic earner. This carrier can be PET, nylon, polyethylene or any other carrier suitable for pigment dispersion. Examples are carbon black pigment in a PET carrier and navy blue pigment in a PET carrier. The preferred melt coloring agent is a colored pigment in a polyethylene carrier. The most preferred melt coloring agent is a colored pigment in a PET carrier. The yarns comprising the variable denier filaments can be processed into fabrics which find particular use in draperies, upholstery fabrics, and automotive upholstery applications.
  • The following examples present illustrative but non-limiting embodiments of the present invention
  • Example 1
  • A PET yarn was produced by melt spinning molten PET and winding up the yarn at different winding speeds ranging from 1600 to 2725 mpm. Carbon black pigment in a concentration range up to 0.25 wt. percent was added to the molten PET prior to spinning. The feeder yarns were then drawn at ambient temperature, using a draw ratio range of 1.69 to 2.07, and a draw zone of 24 inches.
    Test Sample Winding Speed (mpm) Birefringence Pigment (wt. %)
    1 1600 0.014 0.10
    2 2000 0.015 0.10
    3 2400 0.023 0.10
    4 2725 0.031 0.10
    5 1600 0.014 0.17
    6 2000 0.015 0.17
    7 2400 0.023 0.17
    8 2725 0.031 0.17
    9 1600 0.014 0.25
    10 2000 0.015 0.25
    11 2400 0.023 0.25
    12 2725 0.031 0.25
  • The yarns produced at these conditions had a random distribution of light and dark sections without the necessity of dyeing, and showed improved dye lightfastness.
  • Example 2
  • A PET yarn was produced by melt spinning molten PET with 0.20 wt. percent navy pigment added to the molten PET prior to spinning. This yarn was wound at 1600 mpm and drawn at ambient temperature at a draw ratio of 2.02 and a draw zone of 24 inches.
    Test Sample Winding Speed (mpm) Birefringence Pigment (wt. %)
    1 1600 0.014 0.10
    2 1600 0.014 0.20
    3 1600 0.014 0.25
  • A yarn with random dark blue and light blue sections was produced, without dyeing, and showing improved dye lightfastness.

Claims (17)

  1. A process for producing a variable denier melt-colored synthetic polymeric filamentous yarn comprising creating a melt- colored polymer mixture, spinning a melt-colored yarn from said synthetic melt- colored polymer mixture, and subjecting said melt-colored synthetic yarn to a thick and thin drawing process so as to produce a filamentous yarn of variable denier having a random distribution of light and dark sections, produced without dyeing and which exhibits improved dye lightfastness.
  2. A process according to Claim 1 wherein the melt-colored synthetic polymer is pigmented at a concentration up to 5 wt. percent.
  3. A process according to Claim 1 wherein said melt-coloring agents are selected from a group comprising carbon black pigment and navy blue pigment.
  4. A process according to Claim 1 wherein the melt-colored synthetic polymer of said melt-colored synthetic polymer mixture is a polyester.
  5. A process according to Claim 1 wherein said polymer is selected from a group comprising:
    poly(ethyleneterephthalate),
    poly(butylene terephthalate),
    poly(ethyleneterephthalate/5-chloroisophthalate)(85/15),
    poly(ethyleneterephthalate/5-[sodium-sulfo] isophthalate)(97/3), or
    poly(cyclohexane-1,4dimethyleneterephthalate/hexahydroterephthalate) (75/25).
  6. A process according to Claim 1 wherein the preferred melt-colored synthetic polymer of said melt-colored polymer mixture is a linear terephthalate polyester.
  7. A process according to Claim 1 wherein said suitable dicarboxylic acids are selected from a group comprising:
    sebacic acid,
    adipic acid,
    isophthalic acid,
    sulfonyl-4,4-dibenzoic acid, or
    2,8-dibenzofurandicarboxylic acid.
  8. A process according to Claim 1 wherein the melt-colored synthetic polymer mixture is spun in a range of from about 1,600 mpm to about 3,000 mpm to form a yarn.
  9. A process according to Claim 1 wherein the thick and thin drawing process takes place at ambient temperature.
  10. A process according to Claim 1 wherein the ambient temperature is in a range from about 15°C to about 30°C.
  11. A process according to Claim 1 wherein the take-up speed is in a range of from about 1,600 to about 4,000 mpm.
  12. A process according to Claim 1 wherein the take-up speed is more preferably from about 1,800 to about 2,800 mpm.
  13. A process according to Claim 1 wherein said birefringence of said feeder yarn is about 0.01 to about 0.05.
  14. A process according to Claim 1 wherein said birefringence of said feeder yarn is more preferably about 0.015 to about 0.031.
  15. A process according to Claim 1 wherein said draw ratio is about 1.27 to about 2.07.
  16. A process according to Claim 1 wherein said draw ratio is more preferably about 1.69 to about 1.97.
  17. An article of manufacture containing filamentous yarn produced according to the process of Claim 1.
EP19910122036 1991-01-07 1991-12-20 Melt-colored thick and thin yarn Withdrawn EP0494432A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US63824691A 1991-01-07 1991-01-07
US638246 1991-01-07

Publications (2)

Publication Number Publication Date
EP0494432A2 true EP0494432A2 (en) 1992-07-15
EP0494432A3 EP0494432A3 (en) 1993-01-27

Family

ID=24559231

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19910122036 Withdrawn EP0494432A3 (en) 1991-01-07 1991-12-20 Melt-colored thick and thin yarn

Country Status (3)

Country Link
EP (1) EP0494432A3 (en)
JP (1) JPH04289217A (en)
CA (1) CA2058830A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010012128A1 (en) * 2008-07-31 2010-02-04 Chen Yiyung Spun dyeing chromatographic fiber and the preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH433588A (en) * 1962-12-26 1967-04-15 Monsanto Chemicals A process for producing a variable denier continuous filament yarn
EP0345733A2 (en) * 1988-06-06 1989-12-13 BASF Corporation Variable denier filaments and method of producing same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH433588A (en) * 1962-12-26 1967-04-15 Monsanto Chemicals A process for producing a variable denier continuous filament yarn
EP0345733A2 (en) * 1988-06-06 1989-12-13 BASF Corporation Variable denier filaments and method of producing same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010012128A1 (en) * 2008-07-31 2010-02-04 Chen Yiyung Spun dyeing chromatographic fiber and the preparation method thereof
EP2309041A1 (en) * 2008-07-31 2011-04-13 Yi Yung Chen Spun dyeing chromatographic fiber and the preparation method thereof
CN102076893A (en) * 2008-07-31 2011-05-25 陈义勇 Spun dyeing chromatographic fiber and the preparation method thereof
EP2309041A4 (en) * 2008-07-31 2012-01-18 Yi Yung Chen Spun dyeing chromatographic fiber and the preparation method thereof

Also Published As

Publication number Publication date
CA2058830A1 (en) 1992-07-08
EP0494432A3 (en) 1993-01-27
JPH04289217A (en) 1992-10-14

Similar Documents

Publication Publication Date Title
US4826949A (en) High shrinkage polyester fibers and method of preparation
KR100901325B1 (en) Polylatic acid fiber
US6689461B2 (en) False twisted yarn of polyester composite fiber and method for production thereof
US3454460A (en) Bicomponent polyester textile fiber
EP0984086B1 (en) Process for producing polyester fiber and polyester fiber therefrom
EP2508657A1 (en) Polyester fibers dyeable at ordinary pressure and process for producing same
US3998042A (en) Mixed shrinkage yarn
EP2679709B1 (en) Cationic-dyeable polyester fiber and conjugated fiber
US6620504B2 (en) Thick and thin polyester multifilament yarn
US3927167A (en) Production of mixed shrinkage polyester yarn
US4906519A (en) Variable denier filaments and method of producing same
EP0494432A2 (en) Melt-colored thick and thin yarn
US4835053A (en) Dark dyeing yarn containing polyester fibers and method of preparation
JP2844680B2 (en) Different fineness / different shrinkage mixed fiber and method for producing the same
JP3506500B2 (en) Polyester high shrinkage stress fiber
JPH03241024A (en) Production of cation-dyeable superfine false twist yarn
JP3268906B2 (en) Extra-fine fiber fabric with good coloring
KR100548644B1 (en) Elastic conjugated fiber which has improved warping property wounded on a beam
KR20030054569A (en) A method of preparing for thick and thin polyester filament
JP3285685B2 (en) Polyester multifilament yarn and method for producing the same
JP2003020520A (en) Aliphatic polyester thick and thin yarn and method for producing the same
JPS6290315A (en) Modified polyester fiber and production thereof
JPH09228181A (en) Uneven yarn
JPH02154018A (en) Covering yarn
JP2004218182A (en) Poly(lactic acid) false-twisted yarn and method for producing the same

Legal Events

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

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH DE ES FR GB GR IT LI LU NL SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH DE ES FR GB GR IT LI LU NL SE

17P Request for examination filed

Effective date: 19930330

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

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

18D Application deemed to be withdrawn

Effective date: 19950701