EP1356141B1 - Textile fibre material with a permanent repellent action - Google Patents
Textile fibre material with a permanent repellent action Download PDFInfo
- Publication number
- EP1356141B1 EP1356141B1 EP02718025A EP02718025A EP1356141B1 EP 1356141 B1 EP1356141 B1 EP 1356141B1 EP 02718025 A EP02718025 A EP 02718025A EP 02718025 A EP02718025 A EP 02718025A EP 1356141 B1 EP1356141 B1 EP 1356141B1
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- European Patent Office
- Prior art keywords
- polymer
- ambivalent
- polymer compound
- fiber
- spinnable
- 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.)
- Expired - Lifetime
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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
- D01F6/02—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
- 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
-
- 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
- Y10T428/2913—Rod, strand, filament or fiber
Definitions
- the invention relates to a method for producing a textile fiber, which has a permanent phobic effect.
- Textile materials having phobic properties, in particular for repelling oil, Water and dirt are known in the art.
- fluorine waxes e.g. Impregnating sprays for clothing textiles which are on the fiber surface be sprayed on.
- the network enveloping the fiber can be characterized by the described Tearing in influences.
- the repellent system even dissolves over a large area of the fiber product. This also leads to a reinforced Dirt attachment and thus to an ugly appearance of the top fabric.
- The is currently covered in particular by the fact that only dark cloths Find application.
- what is desired are precisely in this area of application colored fiber products, suitable for the paint color of a motor vehicle.
- thermoplastic fiber in particular Polyolefinmaschine, wherein in the polyolefin melt before the Melt extrusion Fluorcarbonester is introduced.
- This stored Fluorocarbon esters if their nature permits, can be found on the surface concentrate and thereby unfold phobic effects. Because both the Fluorocarbon group as well as the ester group associated hydrocarbon group no connection with the thermoplastic fiber, the lotion is in this case also held purely mechanically in the pulp. A permanent one Phobier Ober is not expected.
- the document WO 95/01 396 describes a melt extrusion of Polymer compositions. These polymer compositions consist of a Mixture of a spinnable component (polypropylene, polyethylene, polyamide, Polyester) and a fluorocarbon. The resulting product of this melt extrusion has permanent phobic effect.
- the document WO 99/05 345 discloses the Further, a process for the production of textile fibers, wherein a fluorine-containing Further, a process for the production of textile fibers, wherein a fluorine-containing Compound and a polymer are mixed in a solvent. The Mixture is then dried and then extruded into a fiber. Also This fiber has a permanent phobic effect.
- the object of the present invention is a production method for a Textile fiber, in which a lasting Phobier Ober is achieved.
- the phobier group in this case is the affine one Remaining group connected to the fiber polymer.
- An attrition of the phobia group is Hardly possible, because at the same time the affine residual group from the fiber polymer composite would have to be torn out.
- Other advantages and features are the Subclaims refer.
- the affine residue groups are groups that have a marked affinity to the Have fiber polymer to produce, for example, a polyacrylonitrile fiber become ambivalent polymer components with nitrile groups as affine Residual groups are preferred.
- fiber polymers polyamides, Polyacrylates, etc.
- Fig. 1a shows a composition.
- the two essential components provided for the production of a textile fiber with permanent repellent effect, namely the spinnable polymer component 1 and the ambivalent polymer compound 2 are mixed.
- the ambivalent polymer compound 2 has two different groups, on the one hand the fluorine-containing polymer chain as Phobier mich 2.1, for example Polytretafluorethylen and on the other hand, the ambivalent polymer compound 2 has an affine residual group 2.2 at the other end.
- This affine residual group 2.2 has the ability to interact with the fiber polymer 1.
- fiber polymer 1 polyacrylonitrile is provided in FIG. 1 a and, as affine residual group 2.2, a hydrocarbon containing nitrile groups.
- Both polymer components 1 and 2 are dissolved in the present example in a solvent 3, in particular a polyalcohol, such as polyether glycol.
- the proportion of polymer components 1 and 2 in the solvent is about 20 to 30% by weight.
- the polyacrylonitrile and the nitrile groups of the affine residual group 2.2 exist van der Waal'sche interactions, whereby the ambivalent polymer compound 2 is held in the fiber composite.
- polymer compounds 2 can also be located inside the fiber, as indicated in FIG. 2. These can only move up to the surface 5, if at the surface 5 a place is free. Although this is not so clear from the figures, the fiber 6 has peripherally, ie on its entire surface 5, polymer groups 2.2 with lapping properties.
- compositions used to prepare the textile fibers may vary depending on Field of application of the fibers contain further additives.
- Of the Composition will be appropriate in such cases Mixed with color pigments.
- admixtures of Stabilizers, quenchers, lubricants or ceramic or metallic Reinforcing fibers conceivable.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Manufacturing & Machinery (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
Die Erfindung bezieht sich auf ein Verfahren zur Herstellung einer Textilfaser, welche eine permanente Phobierwirkung aufweist.The invention relates to a method for producing a textile fiber, which has a permanent phobic effect.
Textilmaterialien mit Phobiereigenschaften, insbesondere zur Abweisung von Öl, Wasser und Schmutz sind aus dem Stand der Technik bekannt. So ist in der EP 0 377 813 ein Verdeckstoff für Kraftfahrzeuge beschrieben, wo zur Erzielung der Phobiereigenschaften das Obergewebe mit einem Phobiermittel, hier ein Polymer auf Basis von Fluorpolymeren, ausgerüstet wird. Weiterhin bekannt sind Fluorwachse, z.B. Imprägniersprays für Bekleidungstextilien, die auf die Faseroberfläche aufgesprüht werden. Nachteilig ist jedoch, dass diese Phobiermittel mit der Zeit wieder abgetragen werden, da sie keine dauerhafte feste Verbindung zur Faseroberfläche besitzen. Textile materials having phobic properties, in particular for repelling oil, Water and dirt are known in the art. So in EP 0 377 813 a top material for motor vehicles described where to achieve the Phobiereigenschaften the upper fabric with a repellent, here a polymer Basis of fluoropolymers, is equipped. Also known are fluorine waxes, e.g. Impregnating sprays for clothing textiles which are on the fiber surface be sprayed on. The disadvantage, however, is that these phobizers with time be removed again, as they do not have a permanent solid connection to Own fiber surface.
Bekannte verbesserte Fluorcarbon-Systeme als Phobiermittel sind mit Harzgruppen (Melaminharze, Polyisocyanate) versehen, welche mit sich selbst vernetzen können. Dies führt dazu, dass nach der Beschichtung der Faser mit diesen Fluorcarbonen die Faser von einem aus den Harzgruppen gebildeten Netz eingehüllt wird (siehe Fig. 3). Die Fluorcarbongruppen ragen aus diesem Netz heraus und entfalten ihre abstoßende Wirkung z.B. gegen Wasser oder Schmutz. Derartige Fluorcarbone kommen beispielsweise bei Autoverdeckstoffen zum Einsatz und haben sich durchaus bewährt. Nachteilig ist, dass der beschriebene Phobiereffekt beim Gebrauch der Autoverdeckstoffe, z.B. durch Abtrieb bei Fahrtwind, durch Friktion von Staub, durch Faltvorgänge und andere Umwelteinwirkungen gemindert wird oder gänzlich verloren geht. Das die Faser umhüllende Netz kann nämlich durch die beschriebenen Einflüsse aufreißen. Damit löst sich das Phobiermittelsystem teilweise sogar großflächig vom Faserprodukt ab. Dies führt auch zu einer verstärkten Schmutzanhaftung und damit zu einem unschönen Aussehen des Verdeckstoffs. Das wird derzeit insbesondere dadurch überdeckt, dass nur dunkle Verdeckstoffe Anwendung finden. Gewünscht sind jedoch gerade in diesem Anwendungsbereich farbige Faserprodukte, passend zur Lackfarbe eines Kraftfahrzeuges.Known improved fluorocarbon systems as repellents are with resin groups (Melamine resins, polyisocyanates) provided, which can crosslink with itself. This results in that after coating the fiber with these fluorocarbons the Fiber is wrapped by a network formed from the resin groups (see Fig. 3). The fluorocarbon groups protrude from this network and unfold their repulsive Effect e.g. against water or dirt. Such fluorocarbons come for example, used for car roofing materials and have quite proven. The disadvantage is that the described Phobiereffekt when using the Car covers, e.g. by downforce at wind, by friction of dust, is mitigated by folding and other environmental effects or entirely get lost. Namely, the network enveloping the fiber can be characterized by the described Tearing in influences. In some cases, the repellent system even dissolves over a large area of the fiber product. This also leads to a reinforced Dirt attachment and thus to an ugly appearance of the top fabric. The is currently covered in particular by the fact that only dark cloths Find application. However, what is desired are precisely in this area of application colored fiber products, suitable for the paint color of a motor vehicle.
Des Weiteren wird in der US 6,063,474 eine thermoplastische Faser, insbesondere Polyolefinfaser beschrieben, wobei in die Polyolefinschmelze vor der Schmelzextrusion Fluorcarbonester eingebracht wird. Diese eingelagerten Fluorcarbonester können, wenn es ihre Natur erlaubt, sich an der Oberfläche konzentrieren und damit Phobierwirkungen entfalten. Da sowohl die Fluorcarbongruppe als auch die zum Ester zugehörige Kohlenwasserstoffgruppe keine Verbindung mit der Thermoplastfaser eingeht, wird das Phobiermittel in diesem Fall ebenso rein mechanisch in der Fasermasse gehalten. Eine dauerhafte Phobierwirkung ist nicht zu erwarten.Furthermore, in US 6,063,474 a thermoplastic fiber, in particular Polyolefinfaser, wherein in the polyolefin melt before the Melt extrusion Fluorcarbonester is introduced. This stored Fluorocarbon esters, if their nature permits, can be found on the surface concentrate and thereby unfold phobic effects. Because both the Fluorocarbon group as well as the ester group associated hydrocarbon group no connection with the thermoplastic fiber, the lotion is in this case also held purely mechanically in the pulp. A permanent one Phobierwirkung is not expected.
Das Dokument WO 95/01 396 beschreibt eine Schmelzextrusion von Polymerzusammensetzungen. Diese Polymerzusammensetzungen bestehen aus einer Mischung einer verspinnbaren Komponente (Polypropylen, Polyäthylen, Polyamid, Polyester) und einem Fluorcarbon. Das entstehende Produkt dieser Schmelzextrusion besitzt permanente Phobierwirkung. Das Dokument WO 99/05 345 offenbart des Weiteren ein Verfahren zur Herstellung von Textilfasern, bei dem eine fluorhaltige Weiteren ein Verfahren zur Herstellung von Textilfasern, bei dem eine fluorhaltige Verbindung und ein Polymer in einem Lösungsmittel vermischt werden. Die Mischung wird anschließend getrocknet und dann zu einer Faser extrudiert. Auch diese Faser hat eine permanente Phobierwirkung. Nachteilig bei der verwendeten Schmelzextrusion ist, dass die Fluorcarbonkomponente aufgrund der homogenen Verteilung in der Schmelze auch in der entstehenden Faser gleichmäßig über den Querschnitt verteilt vorliegt und nur der Anteil der Fluorcarbone, die sich an der Oberfläche befinden, zur Phobierwirkung beiträgt. Des Weiteren ist die Schmelzextrusuion auch nicht auf alle verspinnbaren Polymere anwendbar. Eine Polyacrylnitrilfaser lässt sich durch Schmelzextrusion nicht herstellen.The document WO 95/01 396 describes a melt extrusion of Polymer compositions. These polymer compositions consist of a Mixture of a spinnable component (polypropylene, polyethylene, polyamide, Polyester) and a fluorocarbon. The resulting product of this melt extrusion has permanent phobic effect. The document WO 99/05 345 discloses the Further, a process for the production of textile fibers, wherein a fluorine-containing Further, a process for the production of textile fibers, wherein a fluorine-containing Compound and a polymer are mixed in a solvent. The Mixture is then dried and then extruded into a fiber. Also This fiber has a permanent phobic effect. Disadvantageous in the used Melt extrusion is that the fluorocarbon component due to the homogeneous Distribution in the melt even in the resulting fiber evenly over the Distributed cross-section and only the proportion of fluorocarbons, located at the Surface, contributes to the Phobierwirkung. Furthermore, the Schmelzextrusuion not applicable to all spinnable polymers. A Polyacrylonitrile fiber can not be produced by melt extrusion.
Aufgabe der vorliegenden Erfindung ist ein Herstellungsverfahren für eine Textilfaser, bei der eine dauerhafte Phobierwirkung erzielt wird.The object of the present invention is a production method for a Textile fiber, in which a lasting Phobierwirkung is achieved.
Diese Aufgabe wird durch ein Verfahren zur Herstellung einer Textilfaser gemäß
Anspruch 1 erzielt. Wesentliches Merkmal der durch die Erfindung hergestellten
Textilfaser ist die ambivalente Polymerkomponente, die aus zwei unterschiedlichen
Gruppen zusammengesetzt ist, einerseits der Phobiergruppe und andererseits der zur
Fasermatrix hin affinen Restgruppe.This object is achieved by a method of producing a textile fiber according to
Im Gegensatz zu dem bekannten oben beschriebenen substantiven Systemen, die an der Faseroberfläche aufliegen, ist die Phobiergruppe in diesem Fall über die affine Restgruppe mit dem Faserpolymer verbunden. Ein Abrieb der Phobiergruppe ist kaum möglich, da gleichzeitig die affine Restgruppe aus dem Faserpolymerverbund herausgerissen werden müsste. Weitere Vorteile und Merkmale sind den Unteransprüchen zu entnehmen.In contrast to the known substantive systems described above In the case of the fiber surface, the phobier group in this case is the affine one Remaining group connected to the fiber polymer. An attrition of the phobia group is Hardly possible, because at the same time the affine residual group from the fiber polymer composite would have to be torn out. Other advantages and features are the Subclaims refer.
Als Phobiergruppen sind insbesondere Fluorcarbongruppen vorgesehen, es sind jedoch auch Silikon-Polymere denkbar.As Phobiergruppen particular fluorocarbon groups are provided, there are however, silicone polymers are also conceivable.
Die affine Restgruppen sind Gruppen, die eine deutliche Affinität zu dem Faserpolymer aufweisen, soll beispielsweise eine Polyacrylnitrilfaser hergestellt werden, werden ambivalente Polymerkomponenten mit Nitrilgruppen als affine Restgruppen bevorzugt. Bei der Verwendung anderer Faserpolymere (Polyamiden, Polyacrylaten, u.a.) wären entsprechend der chemischen Struktur des Faserpolymers die affinen Restgruppen für die ambivalente Polymerkomponente auszuwählen.The affine residue groups are groups that have a marked affinity to the Have fiber polymer to produce, for example, a polyacrylonitrile fiber become ambivalent polymer components with nitrile groups as affine Residual groups are preferred. When using other fiber polymers (polyamides, Polyacrylates, etc.) would be according to the chemical structure of the fiber polymer select the affinity residual groups for the ambivalent polymer component.
Eine Zusammensetzung aus einer verspinnbaren Polymerkomponente und einer ambivalenten Polymerverbindung, wobei die affine Restgruppe der ambivalenten Polymerverbindung eine Affinität zur verspinnbaren Polymerkomponente aufweist, kann zur Herstellung von Textilfasermaterial, wie beispielsweise Monofilamenten, Multifilamenten, Fasern, Garne oder Flächengebilde verwendet werden. Dies wird im Folgenden anhand eines Ausführungsbeispiels beschrieben. Es zeigen:
- Fig. 1a bis 1c
- verschiedene Stufen des erfindungsgemäßen Herstellungsprozesses einer Textilfaser,
- Fig. 2
- eine Textilfaser im Schnitt und
- Fig. 3
- eine Textilfaser aus dem Stand der Technik im Schnitt.
- Fig. 1a to 1c
- various stages of the manufacturing process according to the invention of a textile fiber,
- Fig. 2
- a textile fiber in the cut and
- Fig. 3
- a textile fiber from the prior art in section.
Die Fig. 1a zeigt eine Zusammensetzung. Die zwei
bereitgestellten wesentlichen Komponenten zur Herstellung einer Textilfaser mit
permanenter Phobierwirkung, nämlich die verspinnbare Polymerkomponente 1 und
die ambivalente Polymerverbindung 2 werden vermischt. Die ambivalente
Polymerverbindung 2 weist zwei unterschiedliche Gruppen auf, einerseits die
Fluor enthaltende Polymerkette als Phobiergruppe 2.1, beispielsweise
Polytretafluorethylen und andererseits besitzt die ambivalente Polymerverbindung 2
am anderen Ende eine affine Restgruppe 2.2. Diese affine Restgruppe 2.2 hat die
Fähigkeit in Wechselwirkung mit dem Faserpolymer 1 zu treten. Als Faserpolymer 1
ist in Fig. 1a Polyacrylnitril vorgesehen und als affine Restgruppe 2.2 ein
Kohlenwasserstoff mit Nitrilgruppen. Beide Polymerkomponenten 1 und 2 sind im
vorliegenden Beispiel in einem Lösungsmittel 3, insbesondere einem Polyalkohol,
wie beispielsweise Polyetherglykol gelöst. Der Anteil der Polymerkomponenten 1
und 2 im Lösungsmittel beträgt ca. 20 bis 30 Gew%. Nach dem Mischen der
Komponenten 1 und 2 erfolgt das Ausspinnen des Gemischs, wobei das
Lösungsmittel ausgetrieben wird. Die Phobiergruppen 2.1, die vom Faserpolymer 1
abgestoßen werden, orientieren sich bereits in Pfeilrichtung 4, d.h. in Richtung
Faseroberfläche (Fig. 1b). Die Restgruppen 2.2 verlangsamen diesen Prozess
aufgrund ihrer Affinität zum Faserpolymer 1. In Fig. 1c ist die ausgesponnene Faser
zu sehen. Die Phobiergruppen 2.1 ragen aus der Oberfläche 5 der Faser 6 heraus.
Zwischen dem Faserpolymer 1, dem Polyacrylnitril und den Nitrilgruppen der affinen
Restgruppe 2.2 bestehen van der Waal'sche-Wechselwirkungen, wodurch die
ambivalente Polymerverbindung 2 im Faserverbund gehalten wird. Abhängig vom
Gewichtsanteil der Polymerverbindung 2 in der Faser 6, bevorzugt werden 10 bis 15
Gew%, können sich natürlich auch noch Polymerverbindungen 2 innerhalb der Faser
befinden, wie dies in Fig. 2 angedeutet ist. Diese können erst an die Oberfläche 5
nachrücken, wenn an der Oberfläche 5 ein Platz frei ist.
Auch wenn dies aus den Figuren nicht so deutlich wird, die Faser 6 weist
umfangseitig, d.h. auf ihrer gesamten Oberfläche 5, Polymergruppen 2.2 mit
Phobiereigenschaften auf. Fig. 1a shows a composition. The two essential components provided for the production of a textile fiber with permanent repellent effect, namely the
Although this is not so clear from the figures, the
Vergleicht man nun diese erfindungsgemäß hergestellte Faser aus Fig. 2 mit dem Stand der
Technik, dargestellt in Fig. 3, so wird der wesentliche Unterschied deutlich. Auch
bei der bekannten phobierten Faser ragen Fluorcarbone 7.1 von der Oberfläche 5 der
Faser 1 ab und entfalten die Phobierwirkung. Endständig befinden sich jedoch keine
Gruppen, die in der Fasermasse gehalten werden, sondern eine Harzkomponente 7.2,
die mit sich selbst reagiert und das die Faser 6 umspannende Netz 8 bildet. Durch
äußere Einflüsse ist es möglich die Polymerverbindung 7 mit der Phobiergruppe 7.1
aus dem Netz herauszulösen, oder gar Teile des Netzes von der Faser abzureißen. Die
Faser ist an diesen Stellen dann ferner schmutzanfällig.If one then compares this fiber produced according to the invention from FIG. 2 with the state of the art
Technology, shown in Fig. 3, the essential difference becomes clear. Also
In the known phobized fiber, fluorocarbons 7.1 protrude from the
Bei der erfindungsgemäßehergestellte Faser 6 (Fig. 2) ist dies nicht und schon gar nicht in
diesem Ausmaß möglich, da die ambivalente Polymerverbindung 2 über die Gruppen
2.2 mit der Fasermasse 1 verbunden ist.In the case of the fiber 6 (FIG. 2) produced according to the invention, this is not and certainly not at all
this extent possible because the
Die zur Herstellung der Textilfasern eingesetzten Zusammensetzungen aus
Polymerkomponente 1 und ambivalenter Polymerverbindung 2 können je nach
Einsatzgebiet der Fasern weitere Additive enthalten. Bei Bekleidungstextilien und
Stoffen für die Kraftfahrzeugindustrie sind ferner farbige Fasern gewünscht. Der
Zusammensetzung werden in solchen Fällen entsprechende
Farbpigmente zugemischt. Für andere Anwendungen sind Beimischungen von
Stabilisatoren, Quencher, Gleitmitteln oder keramische bzw. metallische
Verstärkungsfasern denkbar. The compositions used to prepare the textile
- 11
- Faserpolymerfiber polymer
- 22
- ambivalente Polymerkomponenteambivalent polymer component
- 2.12.1
- PhobiergruppePhobiergruppe
- 2.22.2
- affine Gruppeaffine group
- 33
- Spinnlösungdope
- 44
- Pfeil in Richtung OberflächeArrow towards the surface
- 55
- Faseroberflächefiber surface
- 66
- Faserfiber
- 77
- Phobiermittel (Stand der Technik)Phobiermittel (prior art)
- 7.17.1
- PhobiergruppePhobiergruppe
- 7.27.2
- Vernetzungsgruppenetworking group
- 88th
- Polymernetz von 7Polymer network of 7
Claims (7)
- Solution spinning process for the production of a textile fibre, which has a permanent repellent action characterised by the steps ofpreparing a spinnable polymer component (1) and an ambivalent polymer compound (2) which contains a repelling group (2.1) and a residual group (2.2) with an affinity for the spinnable polymer component (1),mixing the ambivalent polymer compound (2) with the spinnable polymer component (1) in a solvent andspinning the mixture, wherein the repelling group (2.1) orient themselves in the direction of the surface of the forming fibre and migrate to the surface, on the one hand, while the residual groups (2.2) with an affinity anchor the ambivalent polymer compound (2) in the polymer compound (1), on the other hand, as the solvent is driven off.
- Process according to claim 1, characterised in that up to 20 wt.% of the ambivalent polymer compound (2) are used, based on the total quantity of polymer components prepared, namely the spinnable polymer component (1) and the ambivalent polymer compound (2).
- Process according to claim 1 or 2, characterised in that 20 to 30 wt.% of prepared polymer components, namely the spinnable polymer component (1) and the ambivalent polymer compound (2), are dissolved in the solvent.
- Process according to claims 1 to 3, characterised in that other additives such as light stabilisers, quenchers or colour pigments, are added to the mixture.
- Process according to claims 1 to 4, characterised in that an ambivalent polymer compound (2) with fluorocarbon groups as repelling groups (2.1) and with nitrile groups as the residual group (2.2) having an affinity is used, which is mixed with a polyacrylonitrile polymer as the spinnable polymer component (1).
- Process according to one of claims 1 to 5, characterised in that the forming fibre is processed to form a monofilament, a multifilament, a spun fibre, a staple fibre, a yarn or a flat structure.
- Use of the process according to one of claims 1 to 6 for producing textile fibres for clothing textiles or industrial textiles, particularly for the automobile industry.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK02718025T DK1356141T3 (en) | 2001-01-16 | 2002-01-15 | Textile fiber material with permanently repellent effect |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10101627 | 2001-01-16 | ||
DE10101627A DE10101627B4 (en) | 2001-01-16 | 2001-01-16 | Textile fiber material with permanent phobic effect |
PCT/EP2002/000318 WO2002063078A1 (en) | 2001-01-16 | 2002-01-15 | Textile fibre material with a permanent repellent action |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1356141A1 EP1356141A1 (en) | 2003-10-29 |
EP1356141B1 true EP1356141B1 (en) | 2005-06-01 |
Family
ID=7670641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP02718025A Expired - Lifetime EP1356141B1 (en) | 2001-01-16 | 2002-01-15 | Textile fibre material with a permanent repellent action |
Country Status (7)
Country | Link |
---|---|
US (3) | US20040004305A1 (en) |
EP (1) | EP1356141B1 (en) |
AT (1) | ATE296911T1 (en) |
DE (2) | DE10101627B4 (en) |
ES (1) | ES2239711T3 (en) |
PT (1) | PT1356141E (en) |
WO (1) | WO2002063078A1 (en) |
Families Citing this family (2)
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EP2802622A4 (en) * | 2012-01-13 | 2015-08-26 | Univ Missouri | Low temperature plasma coating for anti-biofilm formation |
DE202014003285U1 (en) * | 2014-04-16 | 2015-04-20 | Nextrusion Gmbh | Ballgames with functional surface for improved playability |
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US3655857A (en) * | 1968-10-02 | 1972-04-11 | Celanese Corp | Process for preparing acrylonitrile polymer solution |
US3899563A (en) * | 1971-12-06 | 1975-08-12 | Allied Chem | Synthetic fibers having improved soil and stain repellency |
DE3333457A1 (en) * | 1983-09-16 | 1985-04-04 | Hoechst Ag, 6230 Frankfurt | PERFLUORALKYL-ANTHRANIL ACID ESTER, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A DIRT-REPELLENT AGENT |
US4968471A (en) * | 1988-09-12 | 1990-11-06 | The Goodyear Tire & Rubber Company | Solution spinning process |
US5459188A (en) * | 1991-04-11 | 1995-10-17 | Peach State Labs, Inc. | Soil resistant fibers |
US5380778A (en) * | 1992-09-30 | 1995-01-10 | Minnesota Mining And Manufacturing Company | Fluorochemical aminoalcohols |
TW376397B (en) * | 1995-12-21 | 1999-12-11 | Du Pont | Fluorinated ester melt additives for thermoplastic fibers |
TW426712B (en) * | 1995-12-21 | 2001-03-21 | Du Pont | Fluorinated diester melt additives for thermoplastic polymers and their uses |
US6127485A (en) * | 1997-07-28 | 2000-10-03 | 3M Innovative Properties Company | High temperature-stable fluorochemicals as hydrophobic and oleophobic additives to synthetic organic polymers |
US6288157B1 (en) * | 1999-05-11 | 2001-09-11 | 3M Innovative Properties Company | Alkylated fluorochemical oligomers and use thereof |
-
2001
- 2001-01-16 DE DE10101627A patent/DE10101627B4/en not_active Withdrawn - After Issue
-
2002
- 2002-01-15 PT PT02718025T patent/PT1356141E/en unknown
- 2002-01-15 EP EP02718025A patent/EP1356141B1/en not_active Expired - Lifetime
- 2002-01-15 WO PCT/EP2002/000318 patent/WO2002063078A1/en active IP Right Grant
- 2002-01-15 AT AT02718025T patent/ATE296911T1/en active
- 2002-01-15 DE DE50203271T patent/DE50203271D1/en not_active Expired - Lifetime
- 2002-01-15 ES ES02718025T patent/ES2239711T3/en not_active Expired - Lifetime
-
2003
- 2003-06-28 US US10/609,198 patent/US20040004305A1/en not_active Abandoned
-
2007
- 2007-01-05 US US11/650,097 patent/US20070126143A1/en not_active Abandoned
-
2009
- 2009-04-24 US US12/386,869 patent/US20090214862A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP1356141A1 (en) | 2003-10-29 |
ES2239711T3 (en) | 2005-10-01 |
ATE296911T1 (en) | 2005-06-15 |
US20040004305A1 (en) | 2004-01-08 |
DE50203271D1 (en) | 2005-07-07 |
DE10101627B4 (en) | 2005-06-02 |
PT1356141E (en) | 2005-08-31 |
WO2002063078A1 (en) | 2002-08-15 |
DE10101627A1 (en) | 2002-08-01 |
US20090214862A1 (en) | 2009-08-27 |
US20070126143A1 (en) | 2007-06-07 |
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