EP0344590A2 - Fibres de polyamides thermoplastiques linéaires et de polyphénylènethers modifiés - Google Patents
Fibres de polyamides thermoplastiques linéaires et de polyphénylènethers modifiés Download PDFInfo
- Publication number
- EP0344590A2 EP0344590A2 EP89109325A EP89109325A EP0344590A2 EP 0344590 A2 EP0344590 A2 EP 0344590A2 EP 89109325 A EP89109325 A EP 89109325A EP 89109325 A EP89109325 A EP 89109325A EP 0344590 A2 EP0344590 A2 EP 0344590A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- melt
- polyamide
- mixing
- polyphenylene ether
- 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- Withdrawn
Links
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
- D01F6/88—Monocomponent 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
- D01F6/90—Monocomponent 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
-
- 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
- D01F6/88—Monocomponent 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
- D01F6/94—Monocomponent 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 other polycondensation products
Definitions
- Threads made of polyamides such as polyamide-6 or polyamind-6,6 are industrially manufactured on a large scale and are characterized by high tear strength, bending strength, abrasion resistance, high elasticity and sufficient chemical resistance.
- the disadvantage is their high water absorption and the associated influence on the mechanical properties such.
- B. the modulus of elasticity and associated reduced rigidity due to absorbed water.
- the light and heat stability of these threads is low, which can only be improved over a limited time by adding stabilizers.
- the spinning of polyamide-6,6 in particular requires special measures because of the low thermal stability of the melt, e.g. Steam spinning.
- the previously known measures e.g. The addition of stabilizers to remedy these disadvantages has so far been unsatisfactory.
- the new threads are characterized by improved heat and light stability and low water absorption, while maintaining the mechanical properties.
- the new threads can be spun from the melt without fear of thermal degradation of the melt.
- the threads according to the invention contain 99 to 1% by weight, in particular 50 to 20% by weight, of a linear polyamide e.g. with a relative viscosity of 2.2 to 4.5 measured as a 1% by weight solution in 96% by weight sulfuric acid at 23 ° C.
- a linear polyamide e.g. with a relative viscosity of 2.2 to 4.5 measured as a 1% by weight solution in 96% by weight sulfuric acid at 23 ° C.
- Polyamides derived from lactams with 7 to 13 ring members such as polycaprolactam, polycaprylactam or polylaurine lactam, and polyamides obtained by reacting dicarboxylic acids with diamines, are preferred.
- Suitable dicarboxylic acids which can also be used in any combination, are, for example, alkanedicarboxylic acids having 6 to 12 carbon atoms, in particular 6 to 10 carbon atoms, terephthalic acid, isophthalic acid.
- Suitable diamines which can also be used in any combination, are, for example, alkanediamines having 4 to 12 carbon atoms, in particular 4 to 8 carbon atoms, and also m-xylylenediamine, bis- (4-aminophenyl) methane. It is also possible to use mixtures of the polyamides mentioned. Polyamide-6, polyamide-6,6 and polyamides, which are composed of hexamethylenediamine and isophthalic acid and terephthalic acid, have acquired particular technical importance.
- the threads according to the invention contain 1 to 99% by weight, in particular 80 to 50% by weight, of a reaction product which can be obtained by mixing in the melt, e.g. at a temperature of 250 to 300 ° C, from 99.9 to 35 wt.%, In particular 50 to 80 wt.% of a linear thermoplastic polyamide (component b1) and 0.1 to 65 wt.%, in particular 50 to 20 wt % of a modified polyphenylene ether (component b2).
- a reaction product which can be obtained by mixing in the melt, e.g. at a temperature of 250 to 300 ° C, from 99.9 to 35 wt.%
- a linear thermoplastic polyamide component b1
- 0.1 to 65 wt.% in particular 50 to 20 wt % of a modified polyphenylene ether (component b2).
- modified polyphenylene esters used as component b2 according to the invention are produced from the following components by mixing in the melt at a temperature of 250 to 350 ° C:
- component b 2.1 99.0 to 70% by weight, in particular 90 to 99% by weight, of a polyphenylene ether, it being possible for up to 50% by weight of the polyphenylene ether to be replaced by vinylaromatic polymers.
- the polyphenylene ethers are compounds based on the 2 and / or 6-position to the oxygen-substituted, in particular disubstituted, polyphenylene oxides, the ether oxygen of one unit being bonded to the benzene nucleus of the adjacent unit. At least 50 units are advantageously linked to one another.
- Suitable polyphenylene ethers preferably have alkyl radicals with 1-4 carbon atoms, in particular methyl radicals, in the 2.6 position to the oxygen.
- Examples include poly (2,6-dimethyl-1,4-phenylene) oxide, poly (2,6-diethyl-1,4-phenylene) oxide, poly (2-methyl-6-ethyl-1,4-polyphenylene ) oxide, poly (2-methyl-6-propyl-1,4-phenylene) oxide, poly (2,6-dipropyl-1,4-phenylene) oxide or poly (2-ethyl-6-propyl-1,4 -phenylene) oxide.
- the polyphenylene ethers used advantageously have an intrinsic viscosity of 0.4-0.7 dl / g (measured in chloroform at 30 ° C.). Polyphenylene ethers which are miscible with styrene are particularly preferred.
- Suitable vinyl aromatic polymers are, for example, polystyrene, polyalphamethylstyrene or polyvinyltoluene, in particular polystyrene.
- Component b 2.2 uses 0.1 to 30% by weight, in particular 1 to 10% by weight, of at least one ⁇ , ⁇ -unsaturated aliphatic dicarboxylic acid, its alkyl ester, its half-ester, half-amide or imide and / or a (meth) acrylamide .
- Particularly suitable are fumaric acid C1 to C4 alkyl esters or the corresponding half-ester, fumaric acid half-imide, maleimide or (meth) acrylamide.
- Fumaric acid, C1 to C4 alkyl esters or the corresponding half ester are particularly preferred.
- Beta.-unsaturated aliphatic carboxylic acid or its esters or vinylaromatic monomers can also be used as further component b 2.3 .
- Particularly preferred are acrylic acid, the C1 to C4 alkyl esters of styrene, alphamethylstryrene or vinyl toluene.
- the threads according to the invention optionally contain conventional additives in effective amounts.
- Fillers, matting agents, dye pigments, stabilizers against degradation by the action of heat, atmospheric oxygen and light may be mentioned as additives.
- the threads according to the invention are advantageously produced as follows.
- Component b2 is produced by mixing and reacting components b 2.1 , b 2.2 and optionally b 2.3 in the melt at a temperature of 250 to 350 ° C., poured into strands and granulated.
- the granules obtained in this way are then reacted in the melt, for example at a temperature of 250 to 350 ° C., with the polyamide component b 1, poured into strands and granulated.
- the granules (B) thus obtained are then mixed with component A in the melt, for example at a temperature of 250-350 ° C., and threads are spun from the melt, for example with a diameter of 100 to 10 ⁇ m.
- the threads are advantageously used at elevated temperatures e.g. Stretched 50 to 150 ° C e.g. 1.5 to 10 times, especially 2 to 5 times.
- the threads according to the invention are suitable for the production of technical or textile fabrics such as woven fabrics, knitted fabrics of all kinds, non-woven nonwovens.
- the average residence time in the extruder was 2.5 minutes.
- the melt was poured into strands, cooled, granulated and dried. 40 parts by weight of the granules obtained in this way were reacted with 66 parts by weight of polyamide-6 with a molecular weight M g of 36,000 in a twin-screw extruder at 280 ° C., the residence time in the extruder being 2 minutes.
- the melt was poured into strands, cooled, granulated and the granules dried.
- component B 50 parts of the reaction product thus obtained (component B) were mixed with 50 parts by weight of polyamide-6 with a relative solution viscosity of 2.63, (measured in a solution of 1 g of polymer in 100 ml of 96% by weight sulfuric acid at 25 ° C. ) mixed at a temperature of 275 ° C in the melt, granulated and dried. The dried granules were then spun in a manner known per se on an extruder melt spinning device at a temperature of 290 ° C. and a take-off speed of 800 m / min. The threads obtained were coldly hidden 2.6 times in a manner known per se.
- the hidden threads had the following properties: Titer: 111/20 dtex Tear resistance: 3.6 cN / dtex Elongation at break: 56.5% E-module: 36000 cN / mm2 Water absorption: 1.0% in the standard climate Heat stability: 34% of the initial strength after heating in air at 190 ° C for three hours Light stability: 40% tear strength, based on the initial strength in the Xenotest 450 after 28 days
- Example 1 was repeated with the difference that only polyamide-6 (component A) was spun into threads.
- the threads spun at 290 ° C and coldly stretched 3.5 times had the following properties: Titer: 75/20 dtex Tear resistance: 3.5 cN / dtex Elongation at break: 26% E-module: 29000 cN / mm2 Water absorption: 1.7% in the standard climate Heat stability: 23% measured as in Example 1
- Light stability 20% tear resistance, based on the initial strength of the Xenotest 450 after 28 days
- Example 2 The polyamide-6,6 used in Example 2 was spun into threads and drawn at a temperature of 290 ° C. as in Example 2 without further additives.
- the threads had the following properties: Titer: 94/1 dtex Tear resistance: 3.0 cN / dtex Elongation at break: 30% E-module: 23 cN / dtex
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3818424 | 1988-05-31 | ||
DE19883818424 DE3818424A1 (de) | 1988-05-31 | 1988-05-31 | Faeden aus linearen thermoplastischen polyamiden und modifizierten polyphenylenethern |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0344590A2 true EP0344590A2 (fr) | 1989-12-06 |
EP0344590A3 EP0344590A3 (fr) | 1991-01-23 |
Family
ID=6355473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19890109325 Withdrawn EP0344590A3 (fr) | 1988-05-31 | 1989-05-24 | Fibres de polyamides thermoplastiques linéaires et de polyphénylènethers modifiés |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0344590A3 (fr) |
JP (1) | JPH02104724A (fr) |
DE (1) | DE3818424A1 (fr) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993013251A1 (fr) * | 1991-12-24 | 1993-07-08 | Allied-Signal Inc. | Monofilament polymere et feutre fabrique a partir de celui-ci |
EP0609792A1 (fr) * | 1993-02-03 | 1994-08-10 | Basf Corporation | Fibres de nylon modifiées |
US5554693A (en) * | 1994-10-11 | 1996-09-10 | General Electric Company | Compositions of polyphenylene ether and polyamide resins containing terpene phenol resins |
US5869572A (en) * | 1986-01-27 | 1999-02-09 | General Electric Company | Polymer mixture which comprises a polyamide, a polyphenylene ether and an agent to improve the impact resistance |
WO2012001537A1 (fr) * | 2010-06-29 | 2012-01-05 | Sabic Innovative Plastics Ip B.V. | Fibre de polyamide-poly(oxyde d'arylène) et procédé pour sa préparation |
US9090999B2 (en) | 2011-09-28 | 2015-07-28 | Sabic Global Technologies B.V. | Polyamide/polyphenylene ether fibers and fiber-forming method |
US20170009385A1 (en) * | 2015-07-07 | 2017-01-12 | Voith Patent Gmbh | Monofilament, fabric and production method |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3950410B2 (ja) * | 2002-12-10 | 2007-08-01 | 名古屋油化株式会社 | 繊維、繊維集合体、繊維集合体成形物 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0046040A1 (fr) * | 1980-08-13 | 1982-02-17 | Asahi Kasei Kogyo Kabushiki Kaisha | Composition résineuse thermoplastique à grande résistance thermique ayant une grande résistance à l'huile et objets formés à partir de cette composition |
EP0253123A1 (fr) * | 1986-06-07 | 1988-01-20 | BASF Aktiengesellschaft | Compositions pour moulage thermoplastique |
US4745157A (en) * | 1986-12-18 | 1988-05-17 | General Electric Company | Impact modification of polyphenylene ether-polyamide compositions |
EP0302485A2 (fr) * | 1987-08-07 | 1989-02-08 | BASF Aktiengesellschaft | Compositions à mouler thermoplastiques |
EP0314000A2 (fr) * | 1987-10-30 | 1989-05-03 | BASF Aktiengesellschaft | Masses à mouler thermoplastiques |
-
1988
- 1988-05-31 DE DE19883818424 patent/DE3818424A1/de not_active Withdrawn
-
1989
- 1989-05-24 JP JP12903389A patent/JPH02104724A/ja active Pending
- 1989-05-24 EP EP19890109325 patent/EP0344590A3/fr not_active Withdrawn
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0046040A1 (fr) * | 1980-08-13 | 1982-02-17 | Asahi Kasei Kogyo Kabushiki Kaisha | Composition résineuse thermoplastique à grande résistance thermique ayant une grande résistance à l'huile et objets formés à partir de cette composition |
EP0253123A1 (fr) * | 1986-06-07 | 1988-01-20 | BASF Aktiengesellschaft | Compositions pour moulage thermoplastique |
US4745157A (en) * | 1986-12-18 | 1988-05-17 | General Electric Company | Impact modification of polyphenylene ether-polyamide compositions |
EP0302485A2 (fr) * | 1987-08-07 | 1989-02-08 | BASF Aktiengesellschaft | Compositions à mouler thermoplastiques |
EP0314000A2 (fr) * | 1987-10-30 | 1989-05-03 | BASF Aktiengesellschaft | Masses à mouler thermoplastiques |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5869572A (en) * | 1986-01-27 | 1999-02-09 | General Electric Company | Polymer mixture which comprises a polyamide, a polyphenylene ether and an agent to improve the impact resistance |
WO1993013251A1 (fr) * | 1991-12-24 | 1993-07-08 | Allied-Signal Inc. | Monofilament polymere et feutre fabrique a partir de celui-ci |
EP0609792A1 (fr) * | 1993-02-03 | 1994-08-10 | Basf Corporation | Fibres de nylon modifiées |
US5559194A (en) * | 1993-02-03 | 1996-09-24 | Basf Corportion | Modified nylon fibers |
US5618885A (en) * | 1993-02-03 | 1997-04-08 | Basf Corporation | Fiber-forming modified polyamide blends |
US5623024A (en) * | 1993-02-03 | 1997-04-22 | Basf Corporation | Process for melt-spinning fibers from modified polyamide blends |
US5554693A (en) * | 1994-10-11 | 1996-09-10 | General Electric Company | Compositions of polyphenylene ether and polyamide resins containing terpene phenol resins |
WO2012001537A1 (fr) * | 2010-06-29 | 2012-01-05 | Sabic Innovative Plastics Ip B.V. | Fibre de polyamide-poly(oxyde d'arylène) et procédé pour sa préparation |
US9090999B2 (en) | 2011-09-28 | 2015-07-28 | Sabic Global Technologies B.V. | Polyamide/polyphenylene ether fibers and fiber-forming method |
US20170009385A1 (en) * | 2015-07-07 | 2017-01-12 | Voith Patent Gmbh | Monofilament, fabric and production method |
Also Published As
Publication number | Publication date |
---|---|
JPH02104724A (ja) | 1990-04-17 |
DE3818424A1 (de) | 1989-12-07 |
EP0344590A3 (fr) | 1991-01-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2445404B2 (de) | Verfahren zum spinnen von faserbildenden polyestern | |
DE1807144A1 (de) | Fibrillierter Faden | |
DE4215609A1 (de) | Thermoplastische Mehrschichtverbunde | |
EP0546332A1 (fr) | Stratifiés en matière thermoplastique | |
EP0344590A2 (fr) | Fibres de polyamides thermoplastiques linéaires et de polyphénylènethers modifiés | |
EP0364893B1 (fr) | Polyamides entièrement aromatiques, procédé pour leur préparation et objets moulés | |
DE3641497A1 (de) | Thermoplastische formmassen auf der basis von polyamiden und polyaryletherketonen | |
EP0358892A2 (fr) | Masses moulées thermoplastiques et résistantes aux chocs à la base de copolymères greffés de polyphénylèneéther et polyamides et procédé pour leur préparation | |
DE1905452A1 (de) | Homogene Polyamidpfropfpolymere | |
DE2625692A1 (de) | Mittel zum flammfestausruesten von kunststoffen | |
DE2712541A1 (de) | Neue polyesteramide | |
EP0424860A2 (fr) | Polyamides entièrement aromatiques, procédé de préparation et produits formés | |
DE3706356A1 (de) | Polyamidgranulat mit aeusserer huelle | |
EP0250760B1 (fr) | Masses à mouler thermoplastiques résistantes aux chocs, à base de polyphénylène-éther modifié de polyocténylène et de polyamide | |
DE4138510A1 (de) | Formmassen enthaltend ein polykondensat | |
DE4423349C2 (de) | Polyamidimidharze, die Isophorondiamin enthalten und Verfahren zu ihrer Herstellung | |
EP0613916A1 (fr) | Masse à mouler à base de poly(éthers d'arylène) ayant des groupes anhydrides terminaux | |
DE2338477A1 (de) | Antistatische polyamidfasern mit verringerter neigung zur noppenbildung | |
DE2352903A1 (de) | Verfahren zur herstellung von mit kohlenstoffasern verstaerkten polyamidharzen | |
DE2448970A1 (de) | Verbesserte antistatische polyamidfaser und verfahren zu ihrer herstellung | |
DE1221009B (de) | Thermoplastisch verarbeitbare Formmasse | |
DE3734645C1 (de) | Formkoerper | |
EP0852246A2 (fr) | Compositions contenant un polyamide aromatique et un fullerène, objets moulés à partir de celles-ci | |
EP0424628A1 (fr) | Compositions de moulage renforcées par des fibres à base d'éther de polyphénylène et procédé de leur fabrication | |
EP0351590A2 (fr) | Masses à mouler thermoplastiques à base de poly(éther de phénylène) modifié et de polyamides |
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): BE CH DE ES FR GB IT LI NL |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): BE CH DE ES FR GB IT LI NL |
|
17P | Request for examination filed |
Effective date: 19901227 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Withdrawal date: 19910320 |