GB2093469A - Polyamide compositions for textile fibres - Google Patents

Polyamide compositions for textile fibres Download PDF

Info

Publication number
GB2093469A
GB2093469A GB8203901A GB8203901A GB2093469A GB 2093469 A GB2093469 A GB 2093469A GB 8203901 A GB8203901 A GB 8203901A GB 8203901 A GB8203901 A GB 8203901A GB 2093469 A GB2093469 A GB 2093469A
Authority
GB
United Kingdom
Prior art keywords
textile fibres
textile
polyetheramides
blocks
fibres according
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Withdrawn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
GB8203901A
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.)
ATO Chimie SA
Original Assignee
ATO Chimie SA
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 ATO Chimie SA filed Critical ATO Chimie SA
Publication of GB2093469A publication Critical patent/GB2093469A/en
Withdrawn legal-status Critical Current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
    • D01F6/78Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
    • D01F6/82Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from polyester amides or polyether amides
    • 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
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/12Polyester-amides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Polyamides (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Woven Fabrics (AREA)

Abstract

The present invention relates to novel compositions formed of a homopolyamide and of polyetheramides, the polyetheramides being obtained by condensing together polyether blocks and polyamide blocks and having molecular weights between 10,000 and 40,000. The compositions are formed into yarns and fibres for textile applications.

Description

SPECIFICATION Textile fibres and materials displaying hydrophilic properties The present invention concerns fibers displaying hydrophilic properties and also covers textile materials made up from these fibers.
Numerous polymers and copolymers are already known to obtain fibers from which textile materials are manufactured. The drawback of these existing textile materials is however that they are rough to the touch and crease easily.
Research in order to obtain textile materials more pleasant to the touch (i.e. a softer touch), and less creasable, has shown that these properties can be particularly obtained from fibres (and thus textile materials which they make up) displaying hydrophilic properties presenting furthermore antistatic properties.
In the past it has been noted that 4-nylon fibers or Ultron fibers (commercial name of antistatic 6,6 textile fibers marketed by the company MONSANTO and whose central channel is intermittently clogged by wax) absorb relatively large amounts of water and thus lead to textile materials having hydrophilic properties, thus only slightly creasable and softer to the touch, and having antistatic properties.
These materials are not however, satisfactory in so far as, on the one hand, 4-nylon tends to decompose easily in spinning conditions and leads to yellow-tinged textile materials and, on the other hand Ultron is relatively expensive to produce, difficult to dye (due to the wax present therein) and easily loses its antistatic properties, properties which are equally important for textile materials.
The present invention concerns fibres suitable for the obtention of a textile material displaying hydrophilic properties, i.e. soft to the touch, similar to that of cotton, and displaying low creasability as well as simultaneously having antistatic properties. These fibers lead to texturable, knittable fibres, to the obtention of textile materials and articles of clothing, easy to dye and having a behaviour similar to that of cellulosic fibres. The textiles materials according to the invention can be boiled, although it is preferable to wash them at temperatures between 300 and 600C.
The present invention concerns textile fibres obtained from a composition formed of a homopolyamide and a polyetheramide, the polyetheramide being formed of the product obtained from condensation in the presence of Ti, Zr or Hf - based catalysts, of polyamide blocks having reactive extremities with polymers blocks having reactive extremifies, sudh as, among others: 1 -- polyamide blocks having dicarboxylic chain-ends with either polyetherdiol blocks, or polyetherdiamine blocks (by cyanoethylation and hydrogenation of polyetherdiol); 2 -- polyamide blocks having diamino chain-ends with polyether blocks having carboxylic chainends, the molecular weight of the said polyetheramides being comprised between 10.000 and 40.000.
According to one embodiment of the invention, polyetheramide is formed of the product obtained from copolycondensation of dicarboxylic polyamides with polyoxyethylenediol.
According to a further embodiment of the invention, the overall content of the said compositions in polyoxyethylenediol is comprised between 1 5 and 50%.
According to another embodiment of the invention, the homopolyamide results from the polycondensation of lactams or amino-acids and preferably comprises a homopolyamide belonging to the list formed from PA-6, PA-6.6, PA-il, PA-i 2, PA-6.9. PA--6.10 and PA-6.12.
By polyetheramides are meant not only block polyetheramides (i.e. formed of blocks displaying a certain chain length of their various constituents) but also statistic polyetheramides (i.e. formed by random chaining of the various monomeric constituents).
The dicarboxylic polyamide is preferably PA-S, PA-6.6, PA-i 1, PA-i 2, PA-6.1 0, PA-6.9 or PA-6.1 2.
According to a further embodiment of the invention, the polyetheramide is prepared according to the method described in French patents 74-18913 and 77-22678 in the name of the applicant, patents cited by way of reference and whose contents should be combined with the present description The said compositions from which the fibers are obtained preferably contain, among others, 0.3 to 0.8% TiO2 as well as the standard ingredients used such as antioxidants, anti-ultraviolets, optical azurers, etc.
The present invention concerns, among others, textile application of these compositions and particularly textile materials obtained from the use of fibers, the swelling capacity of which is comprised between 20 to 80%, and more especially between 20 and 40%.
Other aims and advantages of the present invention will become evident after reading through the following description and examples, given by way of non-limitative illustration.
EXAMPLE 1 In a 1.000 i capacity reactor is charged 1 50 kg dicarboxylic 6-polyamide having an average molecular weight of 1.500 obtained from polycondensation of -caprolactam in the presence of adipic acid. 1 50 kg polyoxyethylenediol having a molecular weight of 1.500 and 0.9 kg tetrabutylorthozirconate are added. The reaction mixture is heated under vacuum of 1 Torr at 1 500 C for 5 hours, with vigorous stirring.
The product (I) obtained displays the following features: intrinsic viscosity 1.30 melting point 1 900C The intrinsic viscosity is determined at 250C in solution containing 0.5 by weight of metracresol.
This product (I) contains 50% by weight polyoxyethylenediol.
In an extruder, 50 parts of product (I) are thereafter mixed with 50 parts of 11 -polyamide homopolymers, of textile grade, in the presence of necessary antioxidant additives and anti-ultraviolets.
The component obtained displays the following physical properties: intrinsic viscosity 1.14 melting point 1 640C The product is thereafter spun with a winding speed of 3.000 mime. A thread or yarn is obtained displaying hydrophilic and antistatic properties of which the properties are shown in the table hereinunder: thread 1 65 dtx-30 brins EXAMPLE 2 In an extruder 30 parts of product (I) are mixed with 70 parts of 11 -polyamide homopolymer of textile grade, in the presence of suitable additives.
The product obtained displays the following physical properties: intrinsic viscosity 1.07 melting point 17500 The product is spun as in Example 1. It displays the properties shown in Table I herninunder.
EXAMPLE 3 According to operating conditions of Example 1, 150 kg dicarboxylic 1 2-polyamide (obtained by polycondensation of dodecalactam in the presence of adipic acid), having a molecular weight of 1.500 are caused to react with 1 50 kg polyoxyethylenediol, having a molecular weight of 1.500, in the presence of 0.9 kg tetrabutylorthozirconate.
Product (II) obtained displays the following characteristics: intrinsic viscosity 1.45 melting point 1700C This product contains 50% by weight of polyoxyethylenediol initially used.
In an extruder, 50% of product (II) is mixed with 50 parts of 1 1-polyamide homopolymer, of textile grade, in the presence of appropriate additives.
The product obtained displays the following physical properties: intrinsic viscosity 1.45 melting point 1700C The product is spun as in Example 1. It displays the properties shown in the table herein-under.
EXAMPLE 4 In an extruder 30 parts of product (II) are mixed with 70 parts of 1 1-polyamide homopolymer, of textile grade, in the presence of appropriate additives.
The product obtained displays the following physical properties: intrinsic viscosity 1.12 melting point 1800C The product is spun as in Example 1. It displays the properties shown in table I herein-under.
EXAMPLE 5 In an extruder 30 parts of product (I) are mixed with 70 parts of 6-polyamide homopolymer, of textile grade, in the presence of suitable additives.
The obtained product displays the following physical properties: intrinsic viscosity 1.10 melting point 2100C The product is spun as in Example 1. It displays the properties indicated in table I, herein-under.
TABLE I
Title Absorption rate Swelling capacity Discharge period Example (dtex) of H2O ( /O) ( /O) (s) 6 pure PA. 11 sample 165 1.1 5,9 1860 1 165 4.3 36.4 3 2 165 2.5 23.5 6 3 165 2.0 23.1 3 4 165 1.9 16.3 8 5 165 3.8 32.5 3 7 ULTRON 165 4.5 16.8 39 8 COTTON 165 6.9 43.4 43 This table contains the obtained results for the different compounds tested in Examples 1 to 5, as well as the obtained results for samples comprising pure 11 -polyamide, Ultron and cotton (Examples 6 to 8). The data determined are the water absorption rate (%), swelling capacity (%) and discharge period (1), (or time required for the semi-discharge to take place).The discharge period is determined under a relative humidity rate of 40% and a temperature of 20"C with the use of the static voltmeter device manufactured by Rothschild. The test sample on which this test is carried out is fixed between the jaws of the device; the potential difference between these clamps is 100 volts and the necessary time is measured for the potential difference to be reduced to 50% its initial power, i.e. 50 volts. The antistatic character is that proportionally better as the discharge period is lower.
In the present description and the claims to which it gives rise is meant by: swelling capacity: the rate of swelling measured after immersion, during 4 hours in distilled water at 200C and then centrifugation, water absorption: weight under normal atmosphere-anhydrous weight x 100 ratio anhydrous weight determined after equilibrium under normal atmosphere (humidity level = 650C, temperature = 200C).
Of course, the present invention is in no way limited to the embodiments described and represented; it can be adapted to numerous variations available to the man skilled in the art, according to the applications forseen and without departing fiom the spirit ofthe invention, as defined in the accompanying claims.

Claims (17)

1. Textile fibres displaying hydrophilic properties obtained from compositions formed of a homopolyamide and a polyetheramide, the polyetheramide being formed of the product of polycondensation, in the absence of Ti, Zr or Hf, based catalysts, of polyamide blocks having reactive extremities with polyether blocks having reactive extremities, such as, among others: 1 -- polyamide blocks having dicarboxylic chain-ends with ether polyetherdiol blocks, or polyetherdiamine blocks (by cyanoethylation and hydrogenation of the polyetherdiol); 2 -- polyamide block having diamino chain-ends with polyether blocks having carboxylic chain-ends, the molecular weight of the said polyetheramides being comprised between 10.000 and 40.000.
2. Textile fibres according to claim 1 , wherein the polyetheramides are block polyetheramides.
3. Textile fibres according to claim 1, wherien the polyetheramides are statistic polyetheramides.
4. Textile fibres according to claim 1, wherein the said compositions are formed of a homopolyamide and a polyetheramide, this polyetheramide being formed of the product of copoiycondensation of dicarboxylic polyamides with polyoxyethylendiols.
5. Textile fibres according to one of claims 1 to 4, wherein the total content of the said compositions in polyoxyethylenediol is comprised between 1 5 and 50%.
6. Textile fibres according to one of claims 1 to 4, wherien the homopolyamide results from the polycondensation of lactams or amino acids.
7. Textile fibres according to claim 6, wherein the homopolyamide belongs to the list formed of PA-S, PA-6.6, PA-i 1, PA-i 2, PA-6.9, PA-6.1 0 and PA-6.1 2.
8. Textile fibres according to one of claims 1 to 7, wherein the carboxylic polyamide comprises PA-S, PA-6.6, PA-Il, PA-i 2, PA-6.10, PA-6.9 orPA-6.12.
9. Textile fibres according to one of claims 1 to 8, wherein their swelling capacity is comprised between 20 to 80%.
10. Textile fibres according to claim 9, wherein the said swelling capacity is comprised between 20 and 40%.
11. Textile materials obtained with the use of textile fibres according to one of claims 1 to 8.
12. Textile fibres substantially as hereinbefore described with reference to Example 1 herein.
1 3. Textile fibres substantially as hereinbefore described with reference to Example 2 herein.
1 4. Textile fibres substantially as hereinbefore described with reference to Example 3 herein.
1 5. Textile fibres substantially as hereinbefore described with reference to Example 4 herein.
16. Textile fibres substantially as hereinbefore described with reference to Example 5 herein.
17. Any novel feature or combination of features described herein.
GB8203901A 1981-02-19 1982-02-10 Polyamide compositions for textile fibres Withdrawn GB2093469A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8103284A FR2500003A1 (en) 1981-02-19 1981-02-19 COMPOSITIONS FORMED OF POLYAMIDE AND POLYETHERAMIDE AND TEXTILE APPLICATION OF THESE COMPOSITIONS

Publications (1)

Publication Number Publication Date
GB2093469A true GB2093469A (en) 1982-09-02

Family

ID=9255389

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8203901A Withdrawn GB2093469A (en) 1981-02-19 1982-02-10 Polyamide compositions for textile fibres

Country Status (8)

Country Link
JP (1) JPS57149512A (en)
KR (1) KR830009278A (en)
BE (1) BE891961A (en)
DE (1) DE3203102A1 (en)
ES (1) ES8302752A1 (en)
FR (1) FR2500003A1 (en)
GB (1) GB2093469A (en)
IT (1) IT1153441B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2592388A1 (en) * 1985-12-30 1987-07-03 Atochem POLYAMIDE, POLYETHERAMIDE AND THERMOPLASTIC ELASTOMER ALLOYS
EP0544249A2 (en) * 1991-11-25 1993-06-02 Teijin Limited Polyamide fibers and process for making polyamide fabric
EP0686390A3 (en) * 1994-06-06 1996-07-24 Johnson & Johnson Consumer Novel compositions for dental floss
CN1910220B (en) * 2004-01-22 2010-12-08 罗狄亚化学公司 Method for production of non-woven surfaces
US8557170B2 (en) 2004-01-22 2013-10-15 Rhodia Operations Process for the manufacture of nonwoven surfaces

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62268816A (en) * 1986-05-14 1987-11-21 Asahi Chem Ind Co Ltd Polyamide yarn having water vapor absorption and production thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5190370A (en) * 1975-02-06 1976-08-07 NIJIKUENSHINHORIAMIDOFUIRUMUNOSEIZOHO
JPS52134677A (en) * 1976-05-04 1977-11-11 Toyo Boseki Method of manufacturing polyamide film
DE2716004C3 (en) * 1977-04-09 1987-01-22 Hüls AG, 4370 Marl Thermoplastic moulding compounds based on polylaurolactam and their use for the manufacture of pipes

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2592388A1 (en) * 1985-12-30 1987-07-03 Atochem POLYAMIDE, POLYETHERAMIDE AND THERMOPLASTIC ELASTOMER ALLOYS
EP0233428A1 (en) * 1985-12-30 1987-08-26 Elf Atochem S.A. Alloys based on polyamide, polyether amide and thermoplastic elastomer
US5883195A (en) * 1985-12-30 1999-03-16 Atochem Thermoplastic polyamide/-polyetheramide/elastomer alloys having improved mechanical properties
EP0544249A2 (en) * 1991-11-25 1993-06-02 Teijin Limited Polyamide fibers and process for making polyamide fabric
EP0544249A3 (en) * 1991-11-25 1993-09-22 Teijin Limited Polyamide fibers and process for making polyamide fabric
EP0686390A3 (en) * 1994-06-06 1996-07-24 Johnson & Johnson Consumer Novel compositions for dental floss
CN1910220B (en) * 2004-01-22 2010-12-08 罗狄亚化学公司 Method for production of non-woven surfaces
US8557170B2 (en) 2004-01-22 2013-10-15 Rhodia Operations Process for the manufacture of nonwoven surfaces

Also Published As

Publication number Publication date
BE891961A (en) 1982-07-29
IT8219735A0 (en) 1982-02-18
ES509784A0 (en) 1983-01-16
JPS57149512A (en) 1982-09-16
FR2500003A1 (en) 1982-08-20
ES8302752A1 (en) 1983-01-16
DE3203102A1 (en) 1982-10-21
KR830009278A (en) 1983-12-19
IT1153441B (en) 1987-01-14

Similar Documents

Publication Publication Date Title
US3882090A (en) Water-soluble polyamides from alkyleneoxy bis(propyl-amine)
US3828010A (en) Water-dissipatable polyesteramides
CA1243161A (en) Self-crimping polyamide filaments
US3509106A (en) Process for the production of a linear fiber-forming polyamide having ether linkages
US3522329A (en) Composition comprising polyester and polyether-polyamide blockcopolymer
CA2127841A1 (en) Diorganopolysiloxane composition with excellent heat resistance
EP0156035B1 (en) Copolymer composition suitable for production of highly hydrophilic synthethic fibers, a process for the preparation thereof, and related fibers and manufactured goods
GB2093469A (en) Polyamide compositions for textile fibres
US3687904A (en) Polyamides
CN113260655A (en) Stain resistant polyamide polymers obtained by high end-capping
US4558097A (en) Nylon comfort fiber containing poly(N,N-dimethylacrylamide)
US4736014A (en) Water-soluble polycoesters, process for their preparation, and their use
US6777496B2 (en) Polymeric additives and polymeric articles comprising said additive
Lofquist et al. Hydrophilic Nylon for Improved Apparel Comfort
US4470914A (en) Polyoxyalkylene lubricants of improved oxidative stability and lower viscosity
CA1094716A (en) Spinning of polypyrrolidone
US3093445A (en) Manufacture of polyamide filaments
IL29940A (en) Composite filaments
US3097181A (en) Composition comprising polypyrrolidone and another polyamide
JP2714463B2 (en) Reduction of carboxyl end groups of polyester by lactim ether
US4458053A (en) Nylon comfort fiber containing poly(N,N-dimethylacrylamide)
KR840001632B1 (en) Process for the wet spinning of polypyrrolidone
CA1051626A (en) Polyurethane hard fiber
IL22061A (en) Nylon-66 having improved dyeability
Martin Structure and Properties of a New Polyester Fiber

Legal Events

Date Code Title Description
WAP Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1)