GB2093469A - Polyamide compositions for textile fibres - Google Patents
Polyamide compositions for textile fibres Download PDFInfo
- 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- Withdrawn
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
- D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
- D01F6/82—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from polyester amides or polyether amides
-
- 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
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/12—Polyester-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.
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)
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)
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)
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 |
-
1981
- 1981-02-19 FR FR8103284A patent/FR2500003A1/en not_active Withdrawn
-
1982
- 1982-01-29 BE BE6/47587A patent/BE891961A/en not_active IP Right Cessation
- 1982-01-30 DE DE19823203102 patent/DE3203102A1/en not_active Withdrawn
- 1982-02-10 GB GB8203901A patent/GB2093469A/en not_active Withdrawn
- 1982-02-17 JP JP57024258A patent/JPS57149512A/en active Pending
- 1982-02-18 IT IT19735/82A patent/IT1153441B/en active
- 1982-02-19 ES ES509784A patent/ES8302752A1/en not_active Expired
- 1982-02-19 KR KR1019820000730A patent/KR830009278A/en unknown
Cited By (8)
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 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |