EP0530119B1 - Fibres à base de mélanges pvc/pvc chloré possèdant des propriétés mécaniques améliorées et files de fibres de ténacité améliorée obtenus à partir de ces fibres - Google Patents
Fibres à base de mélanges pvc/pvc chloré possèdant des propriétés mécaniques améliorées et files de fibres de ténacité améliorée obtenus à partir de ces fibres Download PDFInfo
- Publication number
- EP0530119B1 EP0530119B1 EP92420282A EP92420282A EP0530119B1 EP 0530119 B1 EP0530119 B1 EP 0530119B1 EP 92420282 A EP92420282 A EP 92420282A EP 92420282 A EP92420282 A EP 92420282A EP 0530119 B1 EP0530119 B1 EP 0530119B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pvc
- fibres
- filaments
- temperature
- fact
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 43
- 239000004801 Chlorinated PVC Substances 0.000 title claims description 10
- 238000011282 treatment Methods 0.000 claims abstract description 8
- 239000000835 fiber Substances 0.000 claims description 46
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 238000009835 boiling Methods 0.000 claims description 8
- 238000002788 crimping Methods 0.000 claims description 5
- 238000000578 dry spinning Methods 0.000 claims description 5
- 239000011877 solvent mixture Substances 0.000 claims description 5
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 claims 2
- 238000009941 weaving Methods 0.000 abstract description 7
- 229920000915 polyvinyl chloride Polymers 0.000 description 39
- 229920000642 polymer Polymers 0.000 description 7
- UDHXJZHVNHGCEC-UHFFFAOYSA-N Chlorophacinone Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)C(=O)C1C(=O)C2=CC=CC=C2C1=O UDHXJZHVNHGCEC-UHFFFAOYSA-N 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- DXHPZXWIPWDXHJ-UHFFFAOYSA-N carbon monosulfide Chemical compound [S+]#[C-] DXHPZXWIPWDXHJ-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000007704 transition Effects 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/48—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of halogenated hydrocarbons
-
- 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
- D01F6/08—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 halogenated hydrocarbons
- D01F6/10—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 halogenated hydrocarbons from polyvinyl chloride or polyvinylidene chloride
Definitions
- the present invention relates to filaments, threads, fibers monofilaments and similar synthetic articles made of polyvinyl chloride and polyvinyl chloride superchlorinated. It relates more particularly to yarns and fibers of better mechanical qualities and better fiber yarns toughness obtained from these fibers.
- the fibers thus obtained can withstand temperatures the higher the percentage in polyvinyl chloride superchlorinated in the mixture is high, which has as a consequence a reduction in the residual thermal shrinkage.
- high percentages of superchlorinated polyvinyl chloride significantly increase the cost price of yarns and fibers obtained, all the more so since their production process is discontinuous, in particular the heat treatment of fixing.
- French patent n ° 85.126 / 1.359.178 also recommends the use of mixtures of atactic polyvinyl chloride and polyvinyl chloride superchlorinated in a proportion of 5 to 50% of the mixture and specifies that the fibers obtained can, after spinning and drawing, at place to be stabilized under voltage under the conditions indicated in the main patent, be directly shrunk by heating in a suitable medium, for example boiling water. But, in practice, above-mentioned processing conditions do not allow fibers to be obtained good properties only when the proportion of polyvinyl chloride superchlorinated is relatively large.
- PVC / PVC based fibers have now been found superchlorinated with mechanical characteristics superior to those from the known prior art, a finer title, a permanent crimp, suitable for obtaining yarns of lower titer fibers and strong enough to be used on weaving machines high speed without going through the expensive preparation of a plied.
- the present invention relates to fibers based on a superchlorinated PVC / PVC mixture containing 17 to 20% PVC superchlorinated, strand strength ⁇ 2.3 dtex, a residual shrinkage after oil treatment at 115 ° C for 30 min (ASTM Standard D 210 262 T) ⁇ 6% and which are likely to be obtained by a process by which we spin, by a dry spinning process in a known manner, a solution of a mixture PVC / superchlorinated PVC at a rate of 17-20% of superchlorinated PVC in a mixture carbon sulfide / acetone solvent in a proportion of about 60/40 by volume, stretch the filaments in boiling water at a rate between 3 and 6 X, they are continuously stabilizes under voltage at a temperature between 125 and 140 ° C in the presence of steam under absolute pressure from 1.3 to 3.6 bar for 1 to 3 seconds, the cable thus obtained is mechanically or pneumatically curled in known manner, the crimp is continuously fixed
- the present invention also relates to a method for obtaining fibers based on a mixture of polyvinyl chloride atactic and superchlorinated polyvinyl chloride, at a rate of 17 to 20% by weight of superchlorinated PVC, by dry spinning of a solution of the polymer mixture in a solvent mixture of carbon sulfide / acetone of about 60/40 by volume so known per se, drawing of the filaments in boiling water at a rate between 3 and 6 X, continuous stabilization of the filaments under voltage at a temperature between 125 and 140 ° C, preferably 130-135 ° C in the presence of water vapor at a pressure of 2.7 to 2.8 bar for 1 to 3 seconds, then mechanical or pneumatic crimping of the cable thus obtained in known manner and temperature fixing treatment > 100 ° C in the presence of pressurized steam, continuously, then shrinking in a known manner in boiling water or by any means suitable, then drying in a known manner continuously and cutting in the form fiber.
- the present invention also relates to fiber yarns obtained from the fibers described above, having good tenacity, finer strands than those obtained up to and better textile workability, especially in weaving.
- the fibers according to the invention of obtaining fibers of metric number (NM) 50 (20 tex) which was not possible until then because the fiber titles PVC / superchlorinated PVC were too high to obtain fiber yarns sufficiently fine.
- NM 20 50 tex
- the yarns of fibers have a tenacity of at least 10 or 13 cN / tex which allows them to be woven at great speed.
- essentially atactic polyvinyl chloride is intended to mean vinyl chloride homopolymer having a transition temperature second order generally between 65 and 85 ° C.
- Polychloride of vinyl consists predominantly of the isomeric form atactic, that is to say that it is a polymer whose atoms of chlorine and hydrogen are mostly randomly located on both sides of the chain constituting the skeleton of the molecule. Therefore, such poymer is normally of a non-crystallizable nature.
- Such a polymer is most commonly obtained in the least costly manner by known techniques of mass polymerization, suspension or emulsion temperatures generally above 0 ° C, more generally between 20 and 60 ° C or even more.
- the superchlorinated polyvinyl chloride usable according to the present invention can be obtained for example by chlorination of a polyvinyl chloride suspension in the presence of actinic light, or by high temperature chlorination, or in the presence of radiation active chemicals; it usually has a transition temperature second order of at least 100 ° C.
- the staple fibers according to the present invention have mechanical properties and thermal resistance never obtained until there, thanks to a selection of different elements.
- This state of crystallinity is further improved by the subsequent heat treatments, namely drawing in water boiling at temperatures between 85 and 100 ° C, at a rate between 3 and 6 X, preferably 3.5 - 5 X.
- the drawing of the filaments according to the present invention is generally preceded by preheating, for example in water, to temperatures between 60 and 100 ° C, more generally between 75 and 85 ° C.
- preheating for example in water
- One practical way is to use a heated water bath. Stretching itself can be done in 1 or 2 stages, but prefer to gradually increase the temperature of the filaments by preheating, pre-stretching for example in a bath whose water can be maintained between 70 and 95 ° C then continuous stretching at a temperature of one slightly higher than that of pre-stretching, preferably between 85 and 100 ° C or overall stretch indicated above.
- preheating for example in water
- pre-stretching for example in a bath whose water can be maintained between 70 and 95 ° C then continuous stretching at a temperature of one slightly higher than that of pre-stretching, preferably between 85 and 100 ° C or overall stretch indicated above.
- a rate overall stretch of 6 it's easier to limit the stretch of filaments just after the die,
- a second heat treatment that the filaments undergo contributes to fix the structure of the filaments and to give them their good properties, in particular shrinkage in oil at 115 ° C ⁇ 6%, preferably at 5%, and allow strand titles to be obtained ⁇ 2.3 dtex, preferably ⁇ 2.25. Thanks to a better crystalline state, this treatment can be carried out at temperatures higher than those usually supported by PVC / superchlorinated PVC mixtures.
- the filaments thus stabilized are crimped by any means known mechanical or pneumatic, for example by means of a nozzle such than that described in French patent n ° 83329 addition to FR n ° 1 289 491.
- a nozzle such as that described in French patent n ° 83329 addition to FR n ° 1 289 491.
- the filaments are treated with saturated water vapor at a temperature between 110 and 130 ° C and are simultaneously shrunk and curled which allows better subsequent textile workability.
- the crimp thus produced must be set at high temperature, generally between 110 and 120 ° C, in the presence of steam under pressure for at least 20 seconds, preferably at least 30 seconds, and preferably continuously.
- the permanently crimped filaments are then dried in the usual way, generally at a temperature in the region of 100 ° C.
- the process according to the present invention can be carried out completely continuously since the stretching or even since the dissolution of the polymers until final threads or fibers are obtained. Thereby, it is easy to carry out industrially economically.
- the polymers or solutions spun according to the present application may contain usual fillers such as stabilizers vis-à-vis light, heat, brighteners, pigments, dyes likely to improve some of their properties such as their color, dye affinity, thermal and light stability, electrical resistivity ...
- the values toughness at break, and elongation at break are improved which allows the production of much more efficient fiber yarns, improved wearability. They can also be used for production of knitwear, non-woven articles, alone or mixed with other fibers and can in particular undergo all treatments usual washing and dry cleaning under appropriate conditions.
- Said yarns and fibers according to the invention are furthermore particularly appreciated in the textile sector because of certain properties inherent in the composition of mixtures: non-flammability, resistance to light, chemical inertness and power thermal, electrical and acoustic insulation.
- a polymer solution with a concentration of 28% is prepared. weight, in a 60/40 carbon sulfide / acetone solvent mixture volume.
- the solution thus obtained is filtered and, while being maintained at approximately 70 ° C., is spun through a die comprising 908 0.06 mm diameter holes in a dry spinning cell allowing the continuous recovery of the solvent mixture as described in French Patent No. 913,927.
- the filaments are then preheated in a water bath maintained at 80 ° C then stretched for the first times in a water bath maintained at 85 ° C at a rate of 3.15 X, then stretched a second time in a second water bath maintained at 100 ° C at a rate of 1.2 X (total rate 3.78 X).
- the filaments are then stabilized in continuous under tension in a tube containing saturated steam at 125 ° C under a pressure of 2.32 bar, the inlet and outlet speeds of the filaments being strictly identical, and the residence time in the tube being 2 seconds.
- the filaments then undergo mechanical crimping and free retraction in a nozzle as described in the French patent n ° 83 329 addition to FR n ° 1 289 491 at 120 ° C in the presence of steam of water.
- the filament cable is then steam treated in a device known commercially under the brand name Tow Fix from the lich Anonyme Serracant, continuously, at a temperature of 110 ° C. for 30 seconds, the cable being treated in a densified form. at a rate of 450 kg / m 3 . It is then dried in the usual way in an oven at 105 ° C and will be cut to obtain staple fibers in the usual way.
- Example 1 is reproduced with the exception of the processing of fixing which is carried out under tension in the presence of water vapor at 130 ° C, under a pressure of 2.7 bars. Fiber characteristics obtained are shown in Table 1.
- Example 1 is reproduced with the exception of the fixing treatment which is carried out under tension in the presence of steam at 135 ° C., under a pressure of 3 bars.
- the characteristics of the fibers are listed in the table below; the tests corresponding to examples 1 to 3 were carried out compared to control fibers obtained according to French patent no.
- Example 1 Example 2
- Example 3 Witness title to the strand 2.3 2.26 2.22 2.7 residual shrinkage 115 ° C in oil% 6 5.1 4.2 12 tenacity cN / tex 21.8 22.3 22.9 18 elongation% 36 34 31 65 Young's module kN / m2 5.2 5.35 5.41 2.8 shrinkage stress 10 -2 g / dtex 2.4 2.5 2.6 1.5 shrinking nozzle outlet% 4 3 2 2 final brewing% 15 13 11 11
- the shrinkage stress which expresses the degree of orientation of the yarns is measured by means of a retractometer: the samples of filaments of length 4 cm, assembled in the form of test pieces with a titer of 400 dtex on average (each test being carried out on two test pieces) are subjected, after each of the different stages of stretching, stabilization and finally shrinking, to a temperature rise of 1 ° C per minute, from 30 ° C to 170 ° C.
- the retraction force expressed in 10 -2 g / dtex is measured on each test piece as a function of the temperature.
- This withdrawal constraint or withdrawal force in each case passes through a maximum at a certain temperature. It is this maximum withdrawal force which represents the molecular orientation characteristic of the products, which is designated by withdrawal constraint.
- a fiber whose titer has been determined is subjected to a test until it reaches a fully relaxed state, (detection on the force / elongation curve).
- yarns of fibers are prepared, the characteristics of which are as follows: the invention NM 20 witness the invention NM 50 witness Title (tex) 51.81 52.1 19.65 impossible to achieve NM 19.30 19.19 50.88 CV Uster% 9.57 12.19 15.10 - Imperfections over 1000m: - fine stitches 0 0 27 - - big dots 2 10 43 - - buttons 3 6 68 - breaking force (cN) 696 416.8 208.4 - CV breaking force 6.14 18.8 10.36 - Elongation at break % 26.7 29.3 21.25 - Fracture toughness cN / tex 13.4 8 11.43 -
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Woven Fabrics (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9110704A FR2680525B1 (fr) | 1991-08-23 | 1991-08-23 | Fibres a base de melanges pvc/pvc chlore possedant des proprietes mecaniques ameliorees et files de fibres de tenacite amelioree obtenus a partir de ces fibres. |
FR9110704 | 1991-08-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0530119A1 EP0530119A1 (fr) | 1993-03-03 |
EP0530119B1 true EP0530119B1 (fr) | 1998-04-15 |
Family
ID=9416456
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92420282A Expired - Lifetime EP0530119B1 (fr) | 1991-08-23 | 1992-08-21 | Fibres à base de mélanges pvc/pvc chloré possèdant des propriétés mécaniques améliorées et files de fibres de ténacité améliorée obtenus à partir de ces fibres |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0530119B1 (ja) |
JP (1) | JP2535124B2 (ja) |
AT (1) | ATE165124T1 (ja) |
CA (1) | CA2076586A1 (ja) |
DE (1) | DE69225099T2 (ja) |
ES (1) | ES2117657T3 (ja) |
FR (1) | FR2680525B1 (ja) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1089820C (zh) * | 1997-03-11 | 2002-08-28 | 钟渊化学工业株式会社 | 氯乙烯纤维及其制备方法 |
JP4491414B2 (ja) | 2003-04-04 | 2010-06-30 | 電気化学工業株式会社 | ポリ塩化ビニル繊維、その製造方法及びその用途 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5365422A (en) * | 1976-11-22 | 1978-06-10 | Teijin Ltd | Production of polyvinyl chloride fibers having improved heat resistance |
JPS5444776A (en) * | 1977-09-14 | 1979-04-09 | Matsushita Electric Works Ltd | Electromagnetic contactor |
FR2495646A1 (fr) * | 1980-12-08 | 1982-06-11 | Rhone Poulenc Textile | Fils et fibres de bonnes proprietes a base de melange de polychlorure de vinyle et de polychlorure de vinyle surchlore et procede pour leur obtention |
FR2524475A1 (fr) * | 1982-04-01 | 1983-10-07 | Rhovyl | Solutions a base de polychlorure de vinyle, leur procede d'obtantion et fils et fibres ainsi obtenus |
JPS6452487A (en) * | 1987-08-24 | 1989-02-28 | Nagase Iron Works Co Ltd | Health instrument |
-
1991
- 1991-08-23 FR FR9110704A patent/FR2680525B1/fr not_active Expired - Fee Related
-
1992
- 1992-08-20 JP JP4221732A patent/JP2535124B2/ja not_active Expired - Lifetime
- 1992-08-21 ES ES92420282T patent/ES2117657T3/es not_active Expired - Lifetime
- 1992-08-21 DE DE69225099T patent/DE69225099T2/de not_active Expired - Fee Related
- 1992-08-21 EP EP92420282A patent/EP0530119B1/fr not_active Expired - Lifetime
- 1992-08-21 CA CA002076586A patent/CA2076586A1/fr not_active Abandoned
- 1992-08-21 AT AT92420282T patent/ATE165124T1/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPH06184813A (ja) | 1994-07-05 |
JP2535124B2 (ja) | 1996-09-18 |
ES2117657T3 (es) | 1998-08-16 |
FR2680525B1 (fr) | 1996-04-12 |
FR2680525A1 (fr) | 1993-02-26 |
EP0530119A1 (fr) | 1993-03-03 |
DE69225099T2 (de) | 1998-11-26 |
CA2076586A1 (fr) | 1993-02-24 |
ATE165124T1 (de) | 1998-05-15 |
DE69225099D1 (de) | 1998-05-20 |
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