EP1772542A1 - Textile fibers having soft hand characteristics and methods of making thereof - Google Patents

Textile fibers having soft hand characteristics and methods of making thereof Download PDF

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Publication number
EP1772542A1
EP1772542A1 EP06019578A EP06019578A EP1772542A1 EP 1772542 A1 EP1772542 A1 EP 1772542A1 EP 06019578 A EP06019578 A EP 06019578A EP 06019578 A EP06019578 A EP 06019578A EP 1772542 A1 EP1772542 A1 EP 1772542A1
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EP
European Patent Office
Prior art keywords
fiber
additive
formula
forming polymer
present
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Withdrawn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
EP06019578A
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German (de)
French (fr)
Inventor
Kay M. Mccoy
Jeffrey T. Langley
Frank Norman Tuller
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.)
Cognis IP Management GmbH
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Cognis IP Management GmbH
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Filing date
Publication date
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Publication of EP1772542A1 publication Critical patent/EP1772542A1/en
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/46—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
    • 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
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/10—Other agents for modifying properties
    • 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
    • D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
    • D01F6/06—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins from polypropylene
    • 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
    • D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/18—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
    • 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
    • D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
    • 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
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2904—Staple length fiber

Definitions

  • the fiber of the present invention comprises a fiber-forming polymer melt-blended with a bissteramide additive.
  • the fibers of the present invention advantageously possess a lower Stick Slip measurement than a corresponding fiber, which was not treated with the additive used in the present invention.
  • the decrease in Stick Slip measurement of the fibers of the present invention is directly correlated to the softer feel of the fibers achieved by way of the invention.
  • Another aspect of the present invention is a process of making the fiber of the present invention by melt blending a fiber-forming polymer with a bisamide additive, preferably, a bisstearamide additive.
  • the fibers of the present invention have a wide variety of applications in the textile industry, particularly in those textile applications where fibers having a softer feel are valued.
  • the present invention is directed to a fiber having a softer feel, which fiber comprises a fiber-forming polymer melt-blended with a bisamide additive of the formula: wherein R and R" can be the same or different and are straight or branched alkyl groups having from 7 to 19 carbon atoms, R' is a C 2 -C 4 linear alkyl group, preferably ethylene, and x is an integer of from 0 to 5.
  • Preferred compounds of formula I are those having the formula:
  • R and R" have the meanings described above.
  • Compounds in which R and R" contain from 11 to 15 carbon atoms are also of interest, such as DETA bislaurylamide, DETA lauryl/palmityl amide and DETA bispalmitylamide, and the like.
  • Fibers which can be formed by and the fiber-forming polymers which can be used in the present invention include nylon, e.g., Nylon 6 and Nylon 6,6, polyester, polypropylene, acrylic and the like. Any fiber formed by way of the present invention can advantageously achieve a desired softer feel, as compared to the corresponding non-treated fiber.
  • fiber formed from polypropylene by way of the present invention based on the textile industry's desire to utilize a polypropylene fiber.
  • Such fiber advantageously possesses the feel of a nylon fiber.
  • polypropylene is much cheaper than nylon. So it is quite an advantageous accomplishment of the present invention to provide a polypropylene fiber having the soft feel of nylon.
  • the fiber-forming polymer and additive of the present invention are mixed together and processed through an extruder.
  • the extruder will operate at a temperature of from about 140 to about 220°C during the extrusion process.
  • the amount of additive used in the fiber-forming process may range from about 0.25% to about 7% by weight, preferably from about 0.25% to about 2% by weight.
  • the fiber denier may be varied from about 300/144 to about 1540/70.
  • the present invention advantageously provides the ability to tailor the softness of the fiber by way of the combination of fiber diameter and additive content.
  • the additive may additionally provide benefits with respect to texturing bulk performance.
  • pellets of the polymer of interest are melted and conveyed through a heated extruder and then pumped through a spinneret to form a synthetic fiber.
  • the bisamide additive preferably a bisstearamide as described above, can be added and blended with the polymer at the point of extrusion.
  • the additive can be metered as a concentrate into the throat of the extruder at a rate to equal 1% distribution in the final fiber.
  • the additive can be blended with the polymer pellets from a 25% to 50% masterbatch at a ratio to result in a 1% distribution in the final fiber.
  • the polymer with the additive blended therewith can then be processed through typical fiber extrusion conditions to achieve the fibers of the present invention.
  • DETA bisstearamide or N, N'-bisstearamide was blended with polypropylene (PP) resin at the point of extrusion.
  • the blending step was completed either by pre-blending the masterbatch by weight percent with the bulk polymer in the hopper and mechanically mixing the two pellets or by meter feeding the masterbatch pellets into the bulk polymer stream at the throat of the extruder.
  • the PP resin was varied from 14 MFI to 20 MFI.
  • the experiments were carried out over an additive range of 0.25% to 7% by weight.
  • the extrusion profile was 210, 215, 220, and 225°C.
  • the spin beam temperature was 255°C.
  • the fiber denier range was varied from 300/144 to 1540/70.
  • a relative ranking of the hand "feel” of the sample was made.
  • a scale of from 1 to 5 was used wherein a rating of 1 was equivalent to a very soft hand and a rating of 5 was equivalent to a harsh, rough hand.
  • the "Hand” or "feel” of the material was correlated to the Stick Slip (S/S) measurement of fiber friction.
  • the stick slip measurement was completed at a constant sliding velocity of 0.05 cm/min using a pre-tension of 10% of the total yarn denier.
  • the yarn was attenuated around a guide wheel and twisted around itself three times.
  • the stick slip measurement was completed using a Rothschild Friction Meter and yarn take-up device.
  • the friction meter contains the electronics used to measure the ingoing and outgoing tension.
  • the take-up device provides a precise yarn path with tensiometer mounting positions, a guide wheel and a yarn winding wheel that assures constant yarn speed.
  • the two tensiometers used to measure the ingoing and outgoing tension are essentially differential condensers.
  • the tensiometer measuring head consists of three prongs, the middle prong is the moveable measuring rod, which is mounted in a torsion spring that keeps it in a rest position.
  • the two prongs on either side are screwed in yarn guides.
  • the yarn is inserted on top of the measuring rod and during operation the rod is deflected by the moving yarn causing the capacity variations that are transmitted to the friction meter and recorded.
  • N, N'-ethylene bisstearamide was in the form of a small bead.
  • the small bead did not allow for adequate blending with the PP pellets.
  • Blended and Starve Fed by hand to control percentage at 1 to 2%. At greater than 1.5% caused screw slippage.
  • Standapol TM 1433 is a poly(alkyl vinyl ether), which can be obtained from Cognis Corporation.

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

Abstract

This invention relates to a fiber having a softer feel which comprises a fiber-forming polymer melt-blended with a bisamide additive of the formula:
Figure imga0001
 wherein R and R" can be the same or different and are straight or branched alkyl groups having from 7 to 19 carbon atoms, R' is a C2-C4 linear alkyl group, preferably ethylene, and x is an integer of from 0 to 5.

Description

    Background of the invention
  • There is a need in the textile industry to develop and provide a fiber having a softer feel. Traditionally, fibers formed from various polymers have been treated post-extrusion with various spin finish compositions. However, the use of traditional topical spin finishes has not met the need in the textile industry for the desired softer fibers. Some wax-based, topical spin finishes have resulted in softer fiber. However, these wax-based finishes have not been widely accepted or utilized by the industry due to the housekeeping problems caused by the solidification of wax on the machinery.
    • Brief summary of the invention
  • By way of the present invention, it has now been surprisingly found that the above-described need in the textile industry can be advantageously met by providing a fiber having a softer feel, which fiber comprises a fiber-forming polymer melt-blended with a bisamide additive.
  • More particularly, the fiber of the present invention comprises a fiber-forming polymer melt-blended with a bissteramide additive.
    The fibers of the present invention advantageously possess a lower Stick Slip measurement than a corresponding fiber, which was not treated with the additive used in the present invention. The decrease in Stick Slip measurement of the fibers of the present invention is directly correlated to the softer feel of the fibers achieved by way of the invention.
  • Another aspect of the present invention is a process of making the fiber of the present invention by melt blending a fiber-forming polymer with a bisamide additive, preferably, a bisstearamide additive.
  • The fibers of the present invention have a wide variety of applications in the textile industry, particularly in those textile applications where fibers having a softer feel are valued.
    • Detailed description of the invention
  • Other than in the operating examples, or where otherwise indicated, all numbers expressing quantities of ingredients or reaction conditions used herein are to be understood as modified in all instances by the term "about."
  • The present invention is directed to a fiber having a softer feel, which fiber comprises a fiber-forming polymer melt-blended with a bisamide additive of the formula:
    Figure imgb0001
     wherein R and R" can be the same or different and are straight or branched alkyl groups having from 7 to 19 carbon atoms, R' is a C2-C4 linear alkyl group, preferably ethylene, and x is an integer of from 0 to 5.
    • Preferred compounds of formula I are those having the formula:
  • Figure imgb0002
     in which R and R" have the meanings described above. Particularly preferred compounds of formula II are those containing at least one C18 acyl group (R=C17), e.g., DETA bisstearamide (diethylenetriamine bisstearamide), DETA lauryl/stearyl amide and the like. Compounds in which R and R" contain from 11 to 15 carbon atoms are also of interest, such as DETA bislaurylamide, DETA lauryl/palmityl amide and DETA bispalmitylamide, and the like.
  • The most preferred additive is N, N'-ethylene bisstearamide.
    Fibers which can be formed by and the fiber-forming polymers which can be used in the present invention include nylon, e.g., Nylon 6 and Nylon 6,6, polyester, polypropylene, acrylic and the like. Any fiber formed by way of the present invention can advantageously achieve a desired softer feel, as compared to the corresponding non-treated fiber.
  • Particularly preferred is fiber formed from polypropylene by way of the present invention based on the textile industry's desire to utilize a polypropylene fiber. Such fiber advantageously possesses the feel of a nylon fiber. In addition, polypropylene is much cheaper than nylon. So it is quite an advantageous accomplishment of the present invention to provide a polypropylene fiber having the soft feel of nylon.
  • The fiber-forming polymer and additive of the present invention are mixed together and processed through an extruder. Typically, the extruder will operate at a temperature of from about 140 to about 220°C during the extrusion process.
  • The amount of additive used in the fiber-forming process may range from about 0.25% to about 7% by weight, preferably from about 0.25% to about 2% by weight.
  • The fiber denier may be varied from about 300/144 to about 1540/70.
  • Accordingly, the present invention advantageously provides the ability to tailor the softness of the fiber by way of the combination of fiber diameter and additive content. Furthermore, the additive may additionally provide benefits with respect to texturing bulk performance.
  • In the fiber extrusion process carried out by way of the present invention, pellets of the polymer of interest are melted and conveyed through a heated extruder and then pumped through a spinneret to form a synthetic fiber. The bisamide additive, preferably a bisstearamide as described above, can be added and blended with the polymer at the point of extrusion. The additive can be metered as a concentrate into the throat of the extruder at a rate to equal 1% distribution in the final fiber. Alternatively, the additive can be blended with the polymer pellets from a 25% to 50% masterbatch at a ratio to result in a 1% distribution in the final fiber. The polymer with the additive blended therewith can then be processed through typical fiber extrusion conditions to achieve the fibers of the present invention.
  • The invention can be illustrated but not limited by the following examples.
    • Examples
  • DETA bisstearamide or N, N'-bisstearamide was blended with polypropylene (PP) resin at the point of extrusion. The blending step was completed either by pre-blending the masterbatch by weight percent with the bulk polymer in the hopper and mechanically mixing the two pellets or by meter feeding the masterbatch pellets into the bulk polymer stream at the throat of the extruder. The PP resin was varied from 14 MFI to 20 MFI. The experiments were carried out over an additive range of 0.25% to 7% by weight. The extrusion profile was 210, 215, 220, and 225°C. The spin beam temperature was 255°C. The fiber denier range was varied from 300/144 to 1540/70.
  • A relative ranking of the hand "feel" of the sample was made. A scale of from 1 to 5 was used wherein a rating of 1 was equivalent to a very soft hand and a rating of 5 was equivalent to a harsh, rough hand. The "Hand" or "feel" of the material was correlated to the Stick Slip (S/S) measurement of fiber friction.
  • Stick Slip behavior is observed in any sliding system in which the kinetic friction (Fk = force to maintain movement) is less than the static friction (Fs = force to begin movement). Surfaces will "stick" together until a sliding force of Fs is reached, then the surfaces will "slip" over one another at the lower Fk value. This intermittent motion will continually repeat itself at a constant sliding velocity. However, if the sliding velocity is continually increased, the system will eventually reach the point where Fs = Fk and stick slip behavior will cease.
  • For the measurement in the Examples, the stick slip measurement was completed at a constant sliding velocity of 0.05 cm/min using a pre-tension of 10% of the total yarn denier. The yarn was attenuated around a guide wheel and twisted around itself three times. The stick slip measurement was completed using a Rothschild Friction Meter and yarn take-up device. The friction meter contains the electronics used to measure the ingoing and outgoing tension. The take-up device provides a precise yarn path with tensiometer mounting positions, a guide wheel and a yarn winding wheel that assures constant yarn speed. The two tensiometers used to measure the ingoing and outgoing tension are essentially differential condensers. The tensiometer measuring head consists of three prongs, the middle prong is the moveable measuring rod, which is mounted in a torsion spring that keeps it in a rest position. The two prongs on either side are screwed in yarn guides. The yarn is inserted on top of the measuring rod and during operation the rod is deflected by the moving yarn causing the capacity variations that are transmitted to the friction meter and recorded.
  • As shown in the Table 1 below, when compared to the control with no additive, the additive samples all exhibited a significantly lower S/S measurement. When the samples were felt, the samples of the present invention were readily identified as a much softer fiber with a significantly lower S/S value, as compared with the control samples. Table 1
    Sample ID Denier Per Filament Stick Slip S/S cN 0.05cm/mi n Hand Rating F/M Friction cN 300 m/min F/F Friction cN 0.05 cm/min Static Volts
    Control 2 18 71 5 66 121 -16
    *1973@1% 18 23 1 70 93 7
    *1848@1% 18 33 1 69 101 15
    1433@1% 18 66 5 61 115 -10
    1433@3% 18 54 4 67 108 -11
    1433@5% 18 48 3 71 109 -12
    1433@7% 18 24 1 73 86 -11
    Control 22 53 5 58 127 -112
    **1973@0.25% 22 52 5 56 148 -171
    **1973@0.375 % 22 32 4 58 100 -122
    **1973@0.75% 22 36 4 58 124 -95
    **1973@1.0% 22 36 3 57 111 -100
    **1973@1.5% 22 26 3 60 111 -42
    Control tex. 2 10 5 22 26 227
    *1973@3% tex. 2 2 1 23 25 151
    *1973@5% tex. 2 4 2 23 20 190
    1433 flake allowed for adequate blending with the PP pellets allowing a loading of 1, 3, 5 and 7%. At 9% the 1433 caused screw slippage and was not further processed.
    *Standapol™ F 1848, DETA bisstearamide, was provided in powder form from Cognis Brazil.
  • The powder did not allow for adequate blending with the PP pellets.
    Blended and Starve Fed by hand to control percentage at 1 to 2%. At greater than 1.5% caused screw slippage.
  • *CF 1973, N, N'-ethylene bisstearamide, was in the form of a small bead.
    The small bead did not allow for adequate blending with the PP pellets.
    Blended and Starve Fed by hand to control percentage at 1 to 2%. At greater than 1.5% caused screw slippage.
  • **CF1973 in a 25% masterbatch of 20MFI PE. This masterbatch was blended to give the final percentages in the yarn.
  • Standapol™ 1433 is a poly(alkyl vinyl ether), which can be obtained from Cognis Corporation.
  • The results of the Examples clearly demonstrated that the additive unexpectedly allowed for large denier per filament PP to advantageously possess the soft-hand feel of smaller denier PP and nylon fiber. The additive further advantageously and surprisingly did not cause any significant negative changes in the polypropylene fiber strength characteristics.

Claims (11)

  1. A fiber having a softer feel which comprises a fiber-forming polymer melt-blended with a bisamide additive of the formula:
    Figure imgb0003
     wherein R and R" can be the same or different and are straight or branched alkyl groups having from 7 to 19 carbon atoms, R' is a C2-C4 linear alkyl group, preferably ethylene, and x is an integer of from 0 to 5.
  2. The fiber of claim 2 wherein the additive is N, N'-ethylene bisstearamide.
  3. The fiber of claim 1 wherein the additive is of the formula:
    Figure imgb0004
     wherein said formula contains at least one C18 acyl group (R=C17).
  4. The fiber of claim 3 wherein the additive is DETA bisstearamide.
  5. The fiber of claim 3 wherein R and R" of the additive formula contain from 11 to 15 carbon atoms.
  6. The fiber of claim 1 wherein the fiber-forming polymer is selected from the group of polymers consisting of nylon, polypropylene, polyester and acrylic.
  7. The fiber of claim 6 wherein the fiber-forming polymer is polypropylene.
  8. The fiber of claim 1 wherein the additive is present in an amount of from about 0.25% to about 7% by weight.
  9. The fiber of claim 8 wherein the additive is present in an amount of from about 0.25% to about 2%.
  10. The fiber of claim 1, which fiber has a denier ranging from about 300/144 to about 1540/70.
  11. A process of making a fiber having a softer feel, which process comprises melt-blending a fiber-forming polymer with a bisamide additive of the formula:
    Figure imgb0005
     wherein R and R" can be the same or different and are straight or branched alkyl groups having from 7 to 19 carbon atoms, R' is a C2-C4 linear alkyl group, preferably ethylene, and x is an integer of from 0 to 5.
EP06019578A 2005-09-28 2006-09-19 Textile fibers having soft hand characteristics and methods of making thereof Withdrawn EP1772542A1 (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3837022A (en) * 1973-03-30 1974-09-24 Phillips Petroleum Co Fibers for pillow stuffing
JPS58132113A (en) * 1982-01-29 1983-08-06 Toray Ind Inc High-transparency polyamide fiber
US5491004A (en) * 1994-05-26 1996-02-13 Henkel Corporation Process for applying a low soiling fiber finish
WO1998053127A1 (en) * 1997-05-20 1998-11-26 Henkel Corporation Polymer additive for fiber dye enhancement
EP1548161A1 (en) * 2002-08-30 2005-06-29 Toray Industries, Inc. Polylactic acid fiber, yarn package, and textile product

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3413076A (en) * 1962-01-17 1968-11-26 Nippon Rayon Kk Dyeing nitric acid treated formed polypropylene objects containing fatty acid diamides of alkylene diamines
CH464524A (en) * 1963-07-17 1968-10-31 Nippon Rayon Kk Process for improving the dyeability of fibers and molded articles made of polypropylene
US3801521A (en) * 1965-08-27 1974-04-02 Firestone Tire & Rubber Co Spinnable compositions of nylon and a fatty diamide,and drawn articles spun therefrom
JPS5319718B2 (en) * 1972-11-14 1978-06-22
US3801530A (en) * 1973-04-12 1974-04-02 Celanese Corp Stabilized polyalkylene resin composition and process for making same
US5154881A (en) * 1992-02-14 1992-10-13 Hoeganaes Corporation Method of making a sintered metal component
US5525243A (en) * 1994-08-31 1996-06-11 Henkel Corporation High cohesion fiber finishes
US6146494A (en) * 1997-06-12 2000-11-14 The Procter & Gamble Company Modified cellulosic fibers and fibrous webs containing these fibers
DE19754886A1 (en) * 1997-12-10 1999-06-17 Rhone Poulenc Fibres Et Polyme Process for the production of polyurethane elastomer threads and threads produced therefrom
US8013040B2 (en) * 2004-11-08 2011-09-06 Lonza Inc. Cellulose fiber-plastic composition containing a lubricant

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3837022A (en) * 1973-03-30 1974-09-24 Phillips Petroleum Co Fibers for pillow stuffing
JPS58132113A (en) * 1982-01-29 1983-08-06 Toray Ind Inc High-transparency polyamide fiber
US5491004A (en) * 1994-05-26 1996-02-13 Henkel Corporation Process for applying a low soiling fiber finish
WO1998053127A1 (en) * 1997-05-20 1998-11-26 Henkel Corporation Polymer additive for fiber dye enhancement
EP1548161A1 (en) * 2002-08-30 2005-06-29 Toray Industries, Inc. Polylactic acid fiber, yarn package, and textile product

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