EP0816538A2 - Fibres et fils de polyamide à retrait élevé, leur procédé de fabrication et leur utilisation - Google Patents

Fibres et fils de polyamide à retrait élevé, leur procédé de fabrication et leur utilisation Download PDF

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Publication number
EP0816538A2
EP0816538A2 EP97108807A EP97108807A EP0816538A2 EP 0816538 A2 EP0816538 A2 EP 0816538A2 EP 97108807 A EP97108807 A EP 97108807A EP 97108807 A EP97108807 A EP 97108807A EP 0816538 A2 EP0816538 A2 EP 0816538A2
Authority
EP
European Patent Office
Prior art keywords
fibers
shrinkage
shrinking
capro
yarn
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Withdrawn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
EP97108807A
Other languages
German (de)
English (en)
Other versions
EP0816538A3 (fr
Inventor
Gustav Dipl.-Chem. Dr.Rer.Nat. Schuetze
Thomas Dipl.-Ing. Fh Herbst
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.)
Inventa AG fuer Forschung und Patentverwertung
Uhde Inventa Fischer AG
Original Assignee
EMS Inventa AG
Inventa AG fuer Forschung und Patentverwertung
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 EMS Inventa AG, Inventa AG fuer Forschung und Patentverwertung filed Critical EMS Inventa AG
Publication of EP0816538A2 publication Critical patent/EP0816538A2/fr
Publication of EP0816538A3 publication Critical patent/EP0816538A3/fr
Withdrawn legal-status Critical Current

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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
    • D01F6/90Monocomponent 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 polyamides
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G1/00Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics
    • D02G1/12Producing crimped or curled fibres, filaments, yarns, or threads, giving them latent characteristics using stuffer boxes

Definitions

  • the invention relates to shrinking polyamide fibers, a process for their Manufacture and its use in the manufacture of yarn.
  • High shrinkage is desired for polyamide fibers for certain applications.
  • These shrinking fiber types become normal up to 40% shrinking fibers added to a densification of felt or fleece by shrinking or to make bulky fibers for the knitting sector, for voluminous fabrics for women's and men's clothing and textiles To achieve floor coverings and ultimately optimal hosiery yarns (B. Von Falkai (ed.), Synthesefaser, Verlag Chemie (1981), p. 129).
  • the object of the invention was therefore to provide inexpensive, high-shrinkable dyeable materials To develop PA fibers using conventional ones Spinning and drawing technology made and what yarn, in particular Hochbausch carpet yarns and hosiery yarns can be manufactured.
  • the fibers are angled using co-polyamides Monomers synthesized and subjected to a modified crimping process, which is characterized in that the crimp with low cable moisture happens.
  • copolyamides are synthesized using the following monomer units: isophorone diamine, hexamethylene diamine, meta-xylylenediamine, isophthalic acid or adipic acid, at least one of the monomer units having to be angled.
  • monomer units isophorone diamine, hexamethylene diamine, meta-xylylenediamine, isophthalic acid or adipic acid, at least one of the monomer units having to be angled.
  • Preferred combinations are:
  • the relatively highest shrinkage values can be found with the co-polyamides, which the angled monomer units contain isophoronediamine and adipic acid, be preserved.
  • the composition of the shrinking polyamide fibers is 80-95% by weight ⁇ -caprolactam and 5-20% by weight comonomers from the above-mentioned monomer units.
  • the polyamide fibers according to the invention are characterized in that the Thermal shrinkage is over 15%.
  • the fibers of the invention can be produced by a process in which filaments are produced in a manner known per se by melting the monomers in an extruder, the melt emerges from a spinneret, Spinning of the filaments obtained for fibers, drawing, steaming, Crimping and cutting the fibers, the crimping using a crimper is achieved by upsetting and for cooling the Krimper feed rollers and stuffer box dry ice cooling is used.
  • the Dry ice cooling has the advantage that the fibers do not become damp and a premature shrinkage is avoided.
  • copolyamides were produced on a pilot plant scale with an experimental autoclave with a volume of 130 l.
  • the batch quantity per variant was 40 kg.
  • the solution viscosity of the various copolyamide variants in 0.5% m-cresol gave values in the range from 1.93 to 2.08.
  • Composition of the copolyamides (% % by weight) 1.
  • component 2nd component 1 95% Capro + 5% HMD and IPS 2nd 90% Capro + 10% HMD and IPS 3rd 85% Capro + 15% HMD and IPS 4th 95% Capro + 5% MXD and APS 5
  • Capro + 10% MXD and APS 6 95% Capro + 5% IPD and APS 7
  • the co-monomer proportions of the second component were approximate stoichiometric ratio added to the caprolactam.
  • the physical core sizes of the different capolyamides are summarized in Table 2 in comparison to conventional polyamide 6 types (A30 and A34), which are characterized by a different degree of polymerization.
  • the determination of the melting points and the specific melting enthalpy of the investigated polyamides and copolyamides was determined using the Heat flow DSC (Differential Scanning Calorimetry) device TC 11 der Mettler carried out.
  • the polyamide and copolyamide samples were run twice at a heating rate heated from 10K / min and evenly with 5K / min in between cooled down.
  • the melting enthalpy for 100% crystalline PA 6 is 26.0 in the literature kJ / mol, which corresponds to 229.9 J / g, given (Journal of Polymer Science, Part-B, Polymer Physics, Vol. 28, Number 10, pages 2271-2290, 1990)
  • the polymer With a single-screw extruder with 2-zone heating and a conically grooved feed zone, the polymer is drawn in, plasticized and the pressure required to supply the melt pump flanged to the extruder with the required amount of melt.
  • the screw has a diameter of 39.8 mm and an L / D ratio of 15.
  • the spinning pump a gear pump from BARMAG with a throughput of 6 cm 3 / revolution, generates the pressure necessary to pulsate the melt through the heated spinning box and convey it through the capillaries of the spinneret.
  • the filaments fall through an approx. 1.5 m long cross-flow inlet shaft. In this were all Try spinning the filaments with air at 20 ° C and a pressure of 20 mm WS blown.
  • the filaments continue to cool in the subsequent approx. 4 m long chute and after leaving the chute with a preparation roller Spin finish applied to the filaments. Then the spun filaments brought together into a thread, with 2 godets drawn off and wound onto a spool with a winder.
  • Table 3 shows the spinning tests carried out with the associated setting parameters for producing an 11.0 dtex copolyamide high-shrink fiber.
  • the fiber route consists of roller conveyor, net trough, drafting system 1 (S1), steam channel, Drafting unit 2 (S2) and drafting unit 3 (S3) together.
  • the stretch values are 7-roll drafting systems, whereby The drafting system 1 can be heated with water and the drafting system 2 and 3 with steam. The drawn filaments are then wound with a type winder DS 34 Z wound up by DIETZE & SCHELL.
  • the crimped fibers were cut with the GRU-GRU stack cutting machine NEUMAG company cut into staple fibers with a cutting length of 80 mm.
  • Table 6 contains physical characteristics of selected copolyamide filaments before and after the crimping process.
  • the samples were preferably stored for at least 24 hours over phosphorus pentoxide (P 2 O 5 , drying agent) in the desiccator or air-conditioned in a standard climate (20 ° C, 65% relative air humidity).
  • P 2 O 5 phosphorus pentoxide
  • test procedure (I) 8 individual fibers or pieces of yarn with a length of approx. 250 mm are fastened to a special sample frame with a clamping spring. At the lower end of the sample, a fineness-related weight (standard value 100 mg / dtex) is attached, which creates a constant pre-tension in the sample. After determining the initial length L 0 , the test specimens were relieved and "boiled" in boiling water for 5 minutes. After an acclimatization and relaxation time of one hour for fibers and two hours for yarns, the test specimens are loaded again and the length L 1 is read off.
  • the long staple worsted spinning process was used for yarn production Selected using a double card.
  • a polyamide was used as the mixing partner for the high shrink components 6-fiber of the type TS-28-2R with a titer of 6.70 dtex, 80 mm stack length and 0.5 to 3.0% cooking shrinkage is used.
  • This low-shrinking Type was chosen so that the shrinkage and bulk test of the yarn only the influence of the shrinking blend component comes into play.
  • the HS component of mixture 1 is already in the product range of EMS-CHEMIE existing polyamide 6HS fiber with 14.0 dtex, 80 mm stack length and a cooking shrinkage of 10 to 14%.
  • the HS components of mixes 2 and 3 are high-shrinking copolyamides with 11.0 dtex, 80 mm stack length and a cooking shrinkage of up to 27% (Table 8).
  • the thermal shrinkage of spun yarn was done using the crimp construction meter TEXTURMAT from TEXTECHNO.
  • the bulk or crimping of spun yarn after one Heat treatment was performed using the TEXTURMAT crimp contraction measuring device by TEXTECHNO based on DIN 53 840.
  • Each sample variant is first made with a willow (1 m in circumference) 3 skeins of yarn with a precisely defined total titer. These skeins of thread are then hung in a heating cabinet and there 10 Hot air treatment at 120 ° C for minutes. This treatment triggers the shrinkage of the yarn, which results in an increasing Wrinkles or bulk expresses. For the quantitative determination of the The yarn strands become crimped after an acclimatization period of Suspended in the magazine of the crimp contraction measuring device for 2 hours and with a fork in the lower loop of the skeins of thread rests, successively loaded with different forces.
  • the load fork applies a load of 250 cN. After a loading time of 10 seconds, the length L g of the yarn strand is determined and the loading fork swivels back to the starting position in order to load the next yarn strand.
  • the second test cycle begins, in which the length L z of the yarn strands is determined under a load of 2.5 cN.
  • the crimp results in percent and is calculated as the mean of the 3 single measurements and the confidence interval of the mean (95%) specified.
  • the Construction and tensile testing machine DYNAFIL M from TEXTECHNO used for the determination of the shrinking force of the spun yarns.
  • the measuring device essentially consists of a drive part, Heating tube part and measuring head part, with a chart recorder is coupled together.
  • the yarn to be tested is defined with Biasing force led to a two-stage godet, the rear godet (feed godet) feeds the yarn to the measuring zone and the the front interchangeable godet pulls off the yarn.
  • the shrink force measurement is the diameter of the two godets the same size, so that there is no delay between the intake and withdrawal godets arises.
  • the yarn with adjustable thread tension wound on a metal drum After the take-off godet, the yarn with adjustable thread tension wound on a metal drum.
  • the yarn to be examined passes through from the feed godet the heating tube vertically downwards to the force measuring roller, which with a Force sensor is connected.
  • the thread is around the force measuring roller placed and outside the heating pipe back up to the fume cupboard guided.
  • the triggered shrinkage of the yarn as it passes through The heating zone causes a force in the Garnachse, that with the force measuring head determined and given as the shrink force in cN.
  • the statistical certainty of the measured values was determined by the coefficient of variation CV specified.
  • the heating tube was used for the shrinkage force measurements heated to 160 ° C, the largest at this temperature Shrinking forces have occurred.
  • the test speed or the Yarn throughput speed was 10 m / min.
  • the Koch shrinkage of the different yarn types behaves exactly the same, like the Koch shrinkage of the added high shrinkage fibers, i.e. the yarn blend with the highest shrinkage also the most shrinking copolyamide fibers.
  • Yarn mix 4 which contains no high shrinkage fibers (reference variant) shows the lowest shrinkage.
  • the thermal shrinkage at 160 ° is much smaller than the cook shrink.
  • the shrinkage differences between each Mixtures have the same tendency as with cooking shrink.
  • the measurement of the crimp provides similar results for all 4 variants Values and therefore does not allow any information about crimpability and bulk.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Multicomponent Fibers (AREA)
  • Artificial Filaments (AREA)
EP97108807A 1996-05-31 1997-06-02 Fibres et fils de polyamide à retrait élevé, leur procédé de fabrication et leur utilisation Withdrawn EP0816538A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19622027 1996-05-31
DE1996122027 DE19622027C1 (de) 1996-05-31 1996-05-31 Hochschrumpfende PA-Fasern und -Garne und Verfahren zu ihrer Herstellung sowie deren Verwendung

Publications (2)

Publication Number Publication Date
EP0816538A2 true EP0816538A2 (fr) 1998-01-07
EP0816538A3 EP0816538A3 (fr) 1998-04-29

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP97108807A Withdrawn EP0816538A3 (fr) 1996-05-31 1997-06-02 Fibres et fils de polyamide à retrait élevé, leur procédé de fabrication et leur utilisation

Country Status (2)

Country Link
EP (1) EP0816538A3 (fr)
DE (1) DE19622027C1 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030083105A (ko) * 2002-04-19 2003-10-30 주식회사 효성 고수축성 폴리아미드 3원 공중합체 및 이를 이용한고수축성 폴리아미드 섬유
AU2008274592B2 (en) * 2007-07-11 2011-04-21 Electrolux Home Products Corporation N. V. A system and a method for processing a signal from an electric device
WO2015114017A1 (fr) * 2014-01-28 2015-08-06 Radicifil S.P.A. Copolymères à trois composants ayant une transparence élevée et une perméabilité aux gaz faible et son procédé de production
WO2016135129A1 (fr) * 2015-02-23 2016-09-01 Dsm Ip Assets B.V. Fil de polyamide à résistance élevée

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1469155A1 (de) * 1962-08-17 1968-11-28 Vickers Zimmer Ag Verfahren zur Herstellung von vollsynthetischen Zweikomponenten-Faeden und -Fasern
US3554980A (en) * 1965-12-23 1971-01-12 Kanegafuchi Spinning Co Ltd Method for preventing stickiness of fibres consisting of or comprising copolyamide
GB1268374A (en) * 1968-05-29 1972-03-29 Bp Chem Int Ltd Polyamide

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030083105A (ko) * 2002-04-19 2003-10-30 주식회사 효성 고수축성 폴리아미드 3원 공중합체 및 이를 이용한고수축성 폴리아미드 섬유
AU2008274592B2 (en) * 2007-07-11 2011-04-21 Electrolux Home Products Corporation N. V. A system and a method for processing a signal from an electric device
WO2015114017A1 (fr) * 2014-01-28 2015-08-06 Radicifil S.P.A. Copolymères à trois composants ayant une transparence élevée et une perméabilité aux gaz faible et son procédé de production
WO2016135129A1 (fr) * 2015-02-23 2016-09-01 Dsm Ip Assets B.V. Fil de polyamide à résistance élevée
JP2018508663A (ja) * 2015-02-23 2018-03-29 ディーエスエム アイピー アセッツ ビー.ブイ. 高強度ポリアミドヤーン

Also Published As

Publication number Publication date
EP0816538A3 (fr) 1998-04-29
DE19622027C1 (de) 1997-07-31

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