EP1115926A1 - Fils a base de fibres ou de filaments de melanges polymeres, a base de polyterephtalate d'ethylene, de butylene et de trimethylene et leur utilisation - Google Patents

Fils a base de fibres ou de filaments de melanges polymeres, a base de polyterephtalate d'ethylene, de butylene et de trimethylene et leur utilisation

Info

Publication number
EP1115926A1
EP1115926A1 EP99947344A EP99947344A EP1115926A1 EP 1115926 A1 EP1115926 A1 EP 1115926A1 EP 99947344 A EP99947344 A EP 99947344A EP 99947344 A EP99947344 A EP 99947344A EP 1115926 A1 EP1115926 A1 EP 1115926A1
Authority
EP
European Patent Office
Prior art keywords
fibers
ptt
filaments
elongation
yarns
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Withdrawn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
EP99947344A
Other languages
German (de)
English (en)
Inventor
Claudia Fritz
Peter Hirt
Wilhelm Oppermann
Winfried Schuler
Karl-Heinrich Wiese
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.)
Deutsche Institute fuer Textil und Faserforschung Stuttgart
Original Assignee
Deutsche Institute fuer Textil und Faserforschung Stuttgart
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 Deutsche Institute fuer Textil und Faserforschung Stuttgart filed Critical Deutsche Institute fuer Textil und Faserforschung Stuttgart
Publication of EP1115926A1 publication Critical patent/EP1115926A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/92Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters

Definitions

  • the invention relates to yarns made from polymer blend fibers or filaments, comprising the blend components 1) polyethylene terephthalate (PET) or polybutylene terephthalate (PBT) and 2) polytrimethylene terephthalate (PTT) in a mixing ratio of 1): 2) of about 5:95 to 95: 5, in particular from about 10:90 to 90:10, and their use as undyed or dyed yarns for textile fabrics, in particular carpets, knitted fabrics, fabrics, nonwovens or felts.
  • PET polyethylene terephthalate
  • PBT polybutylene terephthalate
  • PTT polytrimethylene terephthalate
  • textile fibers Due to their macromolecular structure, textile fibers exhibit both elastic and viscoelastic behavior (flow behavior) when subjected to tensile stresses in the direction of their fiber axis.
  • flow behavior For the usage properties i.a. the dimensional stability and recovery of the fibers is this behavior in textile fabrics, e.g. of particular importance for carpets.
  • the fibers are subjected to a single or multiple tensile stress and relief between constant elongation limits - an elongation cycle.
  • the residual strain ⁇ R also called permanent strain
  • the elongation information is given as a percentage, this refers to the test length of the fiber equal to 100%, whereby the fiber is under a titer-dependent pretensioning force (here 0.25 cN / tex). Due to the time-dependent relaxation processes in the fibers, after the tensile stress has been released and relieved, waiting times to be defined between the cycles - here: 5 minutes - must be observed before measuring the permanent strains.
  • W. Oppermarm (see above) and H also refer to the good recovery of PTT fibers, as evidenced by cyclical elongation stresses between constant tensile force limits. Traub et al. (Chem. Fibers Int. 45, (1995), 110). Further information on elastic elongation in PA 6, PA 6.6 and PET fibers can be found in B. von Falkai ("Synthesefaser”. Verlag Chemie. Weinheim 1981, ISBN 3-527-25824-8, p. 449; information on measurement technology on page 409).
  • the aforementioned information on the residual elongation SR relates to fibers which are produced from unmodified PET, PBT and PTT. Mixtures of PTT with PET and PTT with PBT are addressed in US-A-4,410,473, US-A-4,454,196 and US-A-4,475,330. US Pat. No. 4,475,330 is concerned only with the production of high-twisted yarns using fibers or filaments of the polymers mentioned and their mixtures. that can be realized via a certain fixing process. The in the US
  • A-4 475 330 described high twisted yarns have the disadvantage that they are unsuitable for fabrics in which no crepe effect is desired.
  • US-A-4 410 473 and US-A-4 454 196 aim to incorporate polymers based on styrene, methyl acrylates or acrylates to produce certain multifilament yarns.
  • Neither of these U.S. patents, nor any other publication, discloses a technical teaching of how to be reduced or maintained at the low level of residual elongation of the PTT fibers while maintaining carrier free dyeability through physical modification, particularly through the use of polymer blends, which affects residual elongation after tensile stress can.
  • the invention is therefore based on the object to provide yarns of the type initially described ⁇ are available which do not show the described disadvantages of the prior art and have improved properties, particularly excellent repetition after deformations or elongations.
  • Particularly advantageous yarns of the type described above with the blend components polybutylene terephthalate (PBT) and polytrimethylene terephthalate (PTT) are characterized in that the fibers or filaments after the first, fifth and tenth
  • Elongation cycle fiber test with 5% and / or 10% total elongation have residual strains ⁇ R that are less than 0.1%.
  • the weft threads have a twist e of 30 to 70 and the warp threads have a twist ⁇ of 80 to 130.
  • Particularly preferred yarns according to the invention are produced on the basis of the methods or filaments described by their production by melt spinning with subsequent preparation application. Melt spinning is carried out in the manner described later, the same also applies to the preparation order.
  • the invention also relates to the use of the specified polymer blend fibers in the form of undyed or dyed fibers or filaments for the production of the yarns according to the invention, the usual procedure being for textile fabrics, in particular carpets, knitted fabrics, fabrics, nonwovens or felts. Turned up
  • Yarns with a twist greater than 300 m "1 are excluded.
  • the fibers or filaments used to manufacture the yarns according to the invention can be dyed with dispersion dyes without pressure and carrier-free at temperatures of about 70 ° C. of the dyeing liquor, high-temperature (HT) dyeings
  • HT high-temperature
  • Granulate mixtures of PET with PTT and PBT with PTT were produced in the following weight ratios (data in% by weight):
  • Tab. 1 Composition of the granulate mixtures for blend fibers
  • PET Type 51, Hoechst, ⁇ re ⁇ 1.84
  • the screw tip was equipped with a dynamic mixing part, the Maddock / Le Roy system and the adjoining cylinder area with two static mixing elements, the Sulzer system.
  • the polymer melt was metered in the spinning head by means of a spinning pump and then filtered in front of the spinneret. The winding took place after preparation with traversing at a frequency-controlled winding speed of 3500 m / min.
  • Tab. 2 Spinning temperatures of the polymer mixtures made of PET and PTT as well as PBT and PTT
  • the staple fibers obtained in this way were drawn using a Zinser (Ebersbach / Fils) drawing system which has three heatable godets and two heating rails in between.
  • the stretching titers were between 65 and 70 dtex, what a delicacy of
  • the initial fineness of the fibers is determined by weighing 100 m of fiber each.
  • the fibers are drawn off the spool using a L 232 winder from Zweigle.
  • 200 mm / min is selected as the clamping length and 200 mm / min as the deformation speed.
  • the jaws are made of Vulkolan and anodized aluminum; the air pressure for generating the clamping pressure is 7 bar. 30 measurements are carried out per sample and the mean value is formed.
  • FIG. 1 shows the schematic tensile force F-strain cycle according to DIN 53835 part 3, ie the schematic representation of a strain cycle with the strains shown: ⁇ o - total strain ⁇ u - elastic strain ⁇ R - residual strain The following residual strains were found for the PBT / PTT blended fibers:
  • Tab. 8 Residual strains ⁇ R of the PBT / PTT blend fibers after 5% and 10% total stretch ⁇ c after the 1st, 5th and 10th cycle.
  • the residual strains R of the PET / PTT blend fibers found after 5% total stretch after the ⁇ 1st cycle, ⁇ 5th cycle, ⁇ 10th cycle (- line) and a course proportional to the composition (- - - lines) are shown. These exceptionally low residual strains are particularly advantageous in applications where good elasticity or repetition is important, such as in carpets, knitted fabrics and fabrics.
  • the knitted fabrics were washed as follows to remove the spin finish:
  • Wash liquor 1 g / 1 Kieralon EDB from Bayer AG.
  • Fleet ratio 1:10
  • the dyeing temperatures were varied between 70 and 130 ° C. The dyeing was always started at 35 ° C and the heating rate was chosen so that the dyeing temperature after 45 min. was achieved. After a dyeing time of 60 min. was with a cooling rate of 1 K / min. cooled to a bath temperature of 40 ° C. Staining conditions: Apparatus: Ahiba Polymat staining time: 60 min. Fleet ratio: 1:50
  • Liquor 0.4 g / 1 dye (2% color) 0.75 g / 1
  • Avolan IS from Bayer AG 1-2 drops of 30% acetic acid (to adjust pH 5-6)
  • the dyeings were reductively treated to remove the dye that had deposited on the fiber surface.
  • the heating rate of the reduction liquor was 2
  • Liquor 2 g / 1 sodium dithionite 4 ml / 1 32.5% by weight sodium hydroxide solution
  • the fibers dyed at different temperatures were extracted with chlorobenzene.
  • the extracts were diluted to a defined volume and the extinctions of the solutions were determined with the aid of a UV-VIS spectrophotometer of the Lambda 7 type from Perkin Elmer in Lake Constance. From the extinction of the extraction solution at the characteristic wavelength.
  • CI Disperse Blue 139 at 604 nm CI Disperse Red 60 at 516 nm the dye content can be determined using the corresponding calibration line.
  • the applied dyeing process with evaluation was developed by HJ.L. Traub described in detail (dissertation, University of Stuttgart, 1994).
  • the maximum determinable dye uptake is about 95% of the maximum possible dye uptake, since the fiber samples are reductively aftertreated before extraction. The dye adhering to the fiber surface is reductively destroyed and the maximum determinable dye content is thereby reduced.
  • the filament yarns obtained were drawn on the one hand on a drawing system from the Zinser company (Ebersbach / Fils), which has three heatable godets and two heating rails in between. No rotation is given here.
  • the Zinser company Ebersbach / Fils
  • Stretching was carried out on a stretching system from Dienes Apparatebau (Mühlheim / Ruhr), a protective rotation having a rotation coefficient ⁇ of approximately 1 being produced.
  • the stretching factors were chosen so that there is an elongation at break of 25%.

Landscapes

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

Abstract

L'invention concerne des fils à base de fibres ou de filaments de mélanges polymères, comprenant comme constituants du mélange : 1) du polytérephtalate d'éthylène (PET) ou du polytérephtalate de butylène (PBT) et 2) du polytérephtalate de triméthylène (PTT) dans un rapport de mélange 1):2) d'approximativement 5:95 à 95:5, notamment d'approximativement 10:90 à 90:10. Ces fils se caractérisent en ce que les fibres ou filaments qui les forment présentent des élongations à la rupture de 15 à 35 % après un ou plusieurs processus d'étirage et, après des vérifications des fibres par cycles d'élongation, avec une élongation totale de 5 %, les fibres ou filaments présentent des élongations résiduelles permanentes ( epsilon R) inférieures à l'élongation résiduelle permanente ( epsilon R) calculée pour le premier cycle d'élongation par l'équation epsilon R [%] = 0,61 - (0,59/100) • X, pour le cinquième cycle d'élongation, par l'équation epsilon R [%] = 0,61 - (0,67/100) • X, pour le dixième cycle d'élongation, par l'équation epsilon R [%] = 0,67 - (0,65/100) • X. Dans ces équations, la variable X désigne la proportion en poids de PTT de l'ordre d'approximativement 5 à 95 % dans les mélanges de fibres ou de filaments avec du PET et du PTT ou dans les mélanges de fibres ou de filaments avec du PBT et du PTT. Les fils ne présentent pas a) de torsion, b) une torsion de fabrication avec un coefficient de torsion métrique alpha de l'ordre de 0,2 à 10 ou c) avec une torsion standard, un coefficient de torsion alpha allant jusqu'à 130. La règle standard DIN 53832 est valable pour le coefficient de torsion alpha et alpha = (t/m• 2ROOT (dtex)/100 est défini. T/m désigne le nombre de torsions par mètre et dtex, la finesse des fibres ou des filaments. L'invention concerne en outre des utilisations avantageuses de ces fils pour produire notamment des tapis, des tissus maille, des tissus, des non-tissés ou des feutres. Ces fils présentent l'avantage d'avoir aussi bien une élongation résiduelle minime après des sollicitations cycliques en élongation, que de ne pas avoir tendance à vriller ou à friser.
EP99947344A 1998-09-14 1999-09-14 Fils a base de fibres ou de filaments de melanges polymeres, a base de polyterephtalate d'ethylene, de butylene et de trimethylene et leur utilisation Withdrawn EP1115926A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19842036 1998-09-14
DE19842036 1998-09-14
PCT/EP1999/006796 WO2000015886A1 (fr) 1998-09-14 1999-09-14 Fils a base de fibres ou de filaments de melanges polymeres, a base de polyterephtalate d'ethylene, de butylene et de trimethylene et leur utilisation

Publications (1)

Publication Number Publication Date
EP1115926A1 true EP1115926A1 (fr) 2001-07-18

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP99947344A Withdrawn EP1115926A1 (fr) 1998-09-14 1999-09-14 Fils a base de fibres ou de filaments de melanges polymeres, a base de polyterephtalate d'ethylene, de butylene et de trimethylene et leur utilisation

Country Status (4)

Country Link
EP (1) EP1115926A1 (fr)
AU (1) AU6082999A (fr)
DE (1) DE19944029C2 (fr)
WO (1) WO2000015886A1 (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101043149B1 (ko) 2002-07-11 2011-06-20 이 아이 듀폰 디 네모아 앤드 캄파니 폴리(트리메틸렌 테레프탈레이트) 섬유, 그의 제조 및 용도
US6921803B2 (en) * 2002-07-11 2005-07-26 E.I. Du Pont De Nemours And Company Poly(trimethylene terephthalate) fibers, their manufacture and use
CN100359057C (zh) * 2004-11-10 2008-01-02 新光合成纤维股份有限公司 自发卷缩性复合纤维及其制造方法
DE102005035767A1 (de) * 2005-07-29 2007-02-01 Deutsche Institute für Textil- und Faserforschung Stuttgart Polyester von Terephthalsäure, ein Verfahren zu deren Herstellung und deren Verwendung
US9809907B2 (en) * 2007-01-02 2017-11-07 Mohawk Carpet, Llc Carpet fiber polymeric blend
WO2010057092A1 (fr) * 2008-11-14 2010-05-20 Peach State Labs, Inc. Compositions de traitement de textiles et de tapis et leurs applications
US20110177283A1 (en) * 2010-01-18 2011-07-21 Futuris Automotive Interiors (Us), Inc. PET Carpet With Additive
KR20130136075A (ko) * 2012-06-04 2013-12-12 현대자동차주식회사 내마모성이 향상된 자동차용 친환경 터프티드 카페트
US10767281B2 (en) * 2016-03-25 2020-09-08 Aladdin Manufacturing Corporation Polyester fiber blends and methods of manufacturing same
EP3835360A1 (fr) * 2019-12-10 2021-06-16 Aladdin Manufacturing Corporation Filaments de polyester ayant une meilleure aptitude à la coloration

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JPS4921256B1 (fr) * 1969-03-12 1974-05-30
US4167541A (en) * 1977-05-12 1979-09-11 Fiber Industries, Inc. Continuous carrierless dyeable polyesters
JPS5761716A (en) * 1980-09-25 1982-04-14 Teijin Ltd Polyester multifilaments and their production
DE3270843D1 (en) * 1982-06-02 1986-06-05 Teijin Ltd High twist polyester multi-filament yarn and fabric made therefrom
US4475330A (en) * 1982-06-03 1984-10-09 Teijin Limited High twist polyester multifilament yarn and fabric made therefrom
MX9603276A (es) * 1994-02-21 1997-03-29 Degussa Un proceso para colorear fibras de tereftalato politrimetileno y el uso de las fibras coloreadas por este proceso.

Non-Patent Citations (1)

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Title
See references of WO0015886A1 *

Also Published As

Publication number Publication date
DE19944029A1 (de) 2000-03-23
WO2000015886A1 (fr) 2000-03-23
DE19944029C2 (de) 2002-06-27
AU6082999A (en) 2000-04-03

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