EP0098485B2 - Kontinuierliches Trockenspinnverfahren für hochschrumpffähige Acrylnitrilfäden und -fasern - Google Patents
Kontinuierliches Trockenspinnverfahren für hochschrumpffähige Acrylnitrilfäden und -fasern Download PDFInfo
- Publication number
- EP0098485B2 EP0098485B2 EP83106188A EP83106188A EP0098485B2 EP 0098485 B2 EP0098485 B2 EP 0098485B2 EP 83106188 A EP83106188 A EP 83106188A EP 83106188 A EP83106188 A EP 83106188A EP 0098485 B2 EP0098485 B2 EP 0098485B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- spinning
- stretching
- filaments
- solvent
- weight
- 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
- 238000010924 continuous production Methods 0.000 title claims description 10
- 238000000578 dry spinning Methods 0.000 title description 10
- 229920002239 polyacrylonitrile Polymers 0.000 title 1
- 238000009987 spinning Methods 0.000 claims description 83
- 239000000835 fiber Substances 0.000 claims description 47
- 238000000034 method Methods 0.000 claims description 43
- 239000002904 solvent Substances 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 9
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
- 239000000314 lubricant Substances 0.000 claims description 6
- 238000002788 crimping Methods 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000000049 pigment Substances 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- 239000000975 dye Substances 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 238000000605 extraction Methods 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 claims description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims 1
- 208000012886 Vertigo Diseases 0.000 description 66
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
- 229920002972 Acrylic fiber Polymers 0.000 description 9
- 238000010411 cooking Methods 0.000 description 9
- 239000000725 suspension Substances 0.000 description 7
- 239000013557 residual solvent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000002166 wet spinning Methods 0.000 description 6
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920002821 Modacrylic Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- -1 alkyl ether sulfates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 210000003934 vacuole Anatomy 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000001043 yellow dye Substances 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
- D01F6/02—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
Definitions
- the invention relates to a continuous process for the production of crimped, highly shrinkable threads and fibers from acrylonitrile copolymers with at least 40% by weight of acrylonitrile units.
- a continuous process is understood according to the invention that the threads are spun, stretched, crimped in one operation without interruption using the method of dry spinning and optionally cut into staple fibers.
- Acrylic fibers are usually manufactured using wet spinning, dry spinning and melt spinning technologies. While continuous processes have become known in the production of acrylic fibers by the wet spinning and melt spinning technology, for example the wet spinning process according to Textile Technology 26 (1976), pages 479-483 or the melt extrusion process according to DE-A-2 627 457, none of which Restriction with regard to the strip weights are so far only a continuous process for the production of acrylic fibers after the dry spinning process has become known, which can only be used for multifilament yarns with low strip weights, so-called acrylic silk and in which certain conditions must be met, in particular a high viscosity Spinning solution (US-A-2 811 409). This process is not suitable for the production of acrylic cables with high tape weights. It is also not suitable for the production of shrink threads and fibers.
- Highly shrinkable threads and fibers are understood to mean threads and fibers with a shrinkage of more than 35%. Such fibers are produced at low degrees of stretch and low stretching temperatures (DE-A-1 435 611 and 2 504 079).
- the dry spinning process is therefore interrupted before drawing, the spinning material is collected in cans, from which it is then fed to further post-treatment (Bela von Falkai, Synthesefaser, Verlag Chemie, Weinheim / Deerfield Beach, Florida / Basel (1981), 3. 204- 206; R. Wiedermann, acrylic fiber spinning and post-treatment process in chemical fibers / textile industry, June 1981, pp. 481-484, in particular p. 482 left column above).
- the object of the present invention to provide a continuous process for the production of highly shrinkable acrylic fibers according to the dry spinning method, in which all process stages from the formation of the thread to the fiber ready for dispatch in one working process without any interruption or intermediate storage, and which can be applied to spinning cables with high strip weights.
- the preparation of the spinning solution should be able to be integrated into the continuous process.
- Spinning draft V is defined as the ratio of take-off speed to spray-out speed S:
- the method of the invention it is possible to produce high-shrinkable spinning tow with a tape weight of 100,000 dtex and more with such a low content of residual solvent that after the hot stretching and the subsequent crimping process, which is carried out at a maximum of 100 ° C, the residual solvent content in the finished fiber or in the continuous cable is clearly below 5% by weight, without the spinning material coming into contact with an extracting agent for the spinning solvent, apart from the water content of the spinning preparation.
- the threads obtained according to the invention have fiber strengths of 1.5 cN / dtex and more.
- Suitable acrylonitrile copolymers are all acrylonitrile copolymers spinnable into so-called acrylic fibers or modacrylic fibers, preferably acrylonitrile copolymers with at least 85% by weight of acrylonitrile units.
- the polymers are known.
- the spinning material ie the spinning cable, which leaves the spinning shaft
- the lubricant he allows perfect stretching of even thick cables of 100,000 dtex and more.
- the preparation can also contain water as an ingredient, but care must be taken that the cable does not absorb more than 10% by weight of moisture. If the cable contains large amounts of water, it cools down very unevenly and during the subsequent stretching, the cable shows tears or wraps on the godets.
- Suitable lubricants are glycols, their derivatives, silicone oils, ethoxylated fatty acids, alcohols, esters, amides, alkyl ether sulfates, and mixtures thereof.
- the preparation can contain a corresponding commercially available preparation, for example a conventional cation-active, anion-active or non-ionic compound, such as a long-chain ethoxylated, sulfated and neutralized alcohol.
- the preparation expediently has a temperature of 50-90 ° C. in order to prevent the hot thread sheet from cooling.
- the chess tapes spun by a spinning machine with, for example, 20 spinning shafts with a total titer of 100,000 dtex and more are prepared in this way, bundled and fed to an inductively heatable roller pair via a take-off device.
- a clamping point is produced by looping the pair of rollers one or more times, if necessary using a lead roller.
- a coolable withdrawal quintet or septet serves as the second clamping point, which is arranged at a distance of approx. 3 m from the inductively heated pair of rollers and causes the cable to be stretched by a correspondingly higher speed.
- the cooling of the rollers on the second stretching element is necessary in order to achieve the desired shrinkage level in the subsequent crimping process.
- Septet rollers which are heatable at the beginning and coolable at the end have proven to be preferred stretching members.
- a tube heated with superheated steam or hot air can advantageously be integrated between the septet rollers.
- spinning take-off speeds of 50-100 m / min are completely sufficient to keep the residual solvent content in the spun material clearly below 10% by weight, so that maximum stretching speeds of 350 m / min are achieved at stretching levels of up to 350%, which is technically are manageable.
- the crimping is preferably carried out in a stuffer box.
- the crimped cable is then cut into staple fibers and pressed into bales.
- the process is particularly suitable for the production of spun-dyed threads and fibers by adding soluble dyes, in particular cationic dyes or pigments, to the spinning solution, because when the color is changed due to the special work-up, considerably less rejects are obtained.
- Solution preparation can also be easily integrated into the continuous process, using conventional solution preparations or in particular the following process:
- a suspension is first prepared at room temperature from the spinning solvent, the polymer and optionally a non-solvent for the polymer which is miscible with the spinning solvent, for example water in an amount of 2 to 20 g per 100 g of polymer.
- This suspension is heated to a temperature which is at least 30 and at most 60 ° C above the temperatures at which the suspension becomes optically homogeneous, i.e. a solution is formed, held at this temperature for 1 to 15 minutes and then immediately fed to the spinning.
- solution polymerization in the spinning solvent used e.g. Dimethylformamide upstream, so that after a corresponding concentration and monomer removal via thin-film evaporator, a continuously working process for the production of high-shrinkable acrylic fibers is achieved for the first time using a dry spinning process with the highest possible degree of automation.
- the spinning solvent used e.g. Dimethylformamide upstream
- a great advantage of the process is that no washing process is required, which means that the drying process previously required is also eliminated.
- the fibers obtained according to the invention have a density of over 1.165 g / cm 3 and are vacuole-stable. Since the high-shrink cable can also be crimped in the dry state, an extraordinarily high adhesion and a very high carding speed, otherwise not known for acrylic high-shrink fibers, in which rain of more than 100 m / min are achieved in the secondary spinning mill. Another advantage of dry heat drawing is the very good stack distribution with extremely low short and long fiber content. All of these advantages are not achieved in conventional processes for producing high-shrinkage fibers as a result of an intermediate washing process for removing spinning solvent.
- dimethylformamide (DMF) are stirred in a kettle at room temperature with 300 kg of an acrylonitrile copolymer made from 93.6% acrylonitrile. 5.7% methyl acrylate and 0.7% sodium methallyl sulfonate with a K value of 81 were mixed.
- the suspension is pumped via a gear pump into a spinning kettle equipped with an agitator. Then the suspension is heated in a double-walled tube with steam of 4.0 bar. The dwell time in the tube is 5 minutes.
- the spinning solution which has a temperature of 138 ° C at the tube outlet and a viscosity of 19 falling ball seconds (8.3 Pa s), measured at 100 ° C, is cooled to 90 ° C after leaving the heating device, filtered and directly one Spinning plant fed with 20 spinning chutes.
- the spinning solution is dry spun from 1264-hole nozzles, nozzle hole diameter 0.2 mm, with a take-off speed of 50 m / min.
- the dwell time of the spinning threads in the spinning shafts is 5 seconds.
- the shaft temperature is 200 ° C and the air temperature is 360 ° C.
- the throughput of air is 40 m 3 / h for each shaft.
- the spinning material with a total titer of 343,000 dtex, which still has a residual solvent content of 2.8% by weight, based on the solids content, is heated to 80-90 ° C immediately after leaving the spinning shafts and before entering the tube connected behind it , aqueous, oil-containing, antistatic preparation so wetted that the oil content of the threads 0.16 wt .-%, the antistatic content 0.04 wt .-%, and the moisture 1.1 wt .-%, based on the fiber solids content , matters.
- the preparation is dosed via gear pumps.
- the tube connected behind the spinning chutes is fed with hot air at 300 ° C in countercurrent to the direction of the thread to remove the DMF. Then the warm cable is sent over a roller septet heated inductively to 145 ° C. The cable assumes a strip temperature of 85 ° C, measured with the KT 15 radiation thermometer. The cable is then stretched by 250%, with a stretch septet with coolable rollers serving as the second clamping point. The strip temperature after the stretching process is 39 ° C. Immediately afterwards, the cable is crimped in a stuffer box and subjected to cold air at room temperature in a U-tube-shaped boot in order to maintain the shrinkage level. Then the high-shrinkable acrylic cable is cut into staple fibers 80 mm long and fed to a pack press.
- the high shrinkable acrylic fibers produced in a continuous process in this way have a single fiber end titre of 5.0 dtex.
- the fiber cooking shrinkage, determined in boiling water, is 44.4%.
- the density before cooking is 1.174 g / cm 3 and after cooking at 1.171 g / cm 3 .
- the fiber strength is 1.8 cN / dtex and the fiber elongation is 70%.
- the fibers are vacuole stable and have a completely smooth, structureless fiber surface.
- the fibers could be pre-processed on a high-performance card at 120 m / min.
- the short and long fiber content in the stack diagram is less than 2%.
- a suspension according to Example 1 is in the spinning kettle with 1.18% by weight, based on solids, of the red dye of the formula: and 0.11% by weight, based on solids, of the yellow dye of the formula: added to achieve a crimson color and then, as described in Example 1, heated, transferred to a spinning solution and spun to crimson high-shrinkage fibers and aftertreated.
- the high shrinkage fibers have a single fiber end titer of 5.1 dtex.
- the fiber cooking shrinkage was 44.8%.
- the density of the crimson high-shrink fibers before cooking is 1.172 g / cm 3 and after cooking at 1.166 g / cm 3 .
- the fiber strength is 1.7 cN / dtex and the fiber elongation is 66%.
- the fibers could be processed on a high-performance card at 110 m / min.
- a suspension according to Example 1 was mixed with 0.04% by weight of carbon black based on solids, 0.02% by weight of pigment red and 0.09% by weight of pigment yellow to achieve a beige color and, as described in Example 1, heated, transferred to a spinning solution and aftertreated. However, it was stretched 1: 3.5 times at a belt temperature of 100 ° C.
- the beige high-shrink fibers with a final diter of 3.8 dtex have a boiling shrinkage of 35.3%.
- the fiber strength is 2.3 cN / dtex and the elongation is 50%.
- the density is 1.172 g / cm 3 before cooking and 1.165 g / cm 3 after cooking.
- the fibers could be processed on the high-performance card at 100 m / min.
Landscapes
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- 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)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19823225268 DE3225268A1 (de) | 1982-07-06 | 1982-07-06 | Kontinuierliches trockenspinnverfahren fuer hochschrumpffaehige acrylnitrilfaeden und -fasern |
DE3225268 | 1982-07-06 |
Publications (4)
Publication Number | Publication Date |
---|---|
EP0098485A2 EP0098485A2 (de) | 1984-01-18 |
EP0098485A3 EP0098485A3 (en) | 1985-09-25 |
EP0098485B1 EP0098485B1 (de) | 1987-01-21 |
EP0098485B2 true EP0098485B2 (de) | 1993-03-31 |
Family
ID=6167768
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83106188A Expired - Lifetime EP0098485B2 (de) | 1982-07-06 | 1983-06-24 | Kontinuierliches Trockenspinnverfahren für hochschrumpffähige Acrylnitrilfäden und -fasern |
Country Status (4)
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3308657A1 (de) * | 1983-03-11 | 1984-09-20 | Bayer Ag, 5090 Leverkusen | Kontinuierliches verfahren zur herstellung von polyacrylnitrilfaeden und -fasern |
DE3630244C2 (de) * | 1986-09-05 | 1994-06-16 | Bayer Ag | Kontinuierliches Trockenspinn- und Nachbehandlungsverfahren des Spinngutes für hochschrumpffähige Acrylnitrilfäden und -fasern und entsprechende Fäden und Fasern |
DE3634753A1 (de) * | 1986-09-05 | 1988-03-17 | Bayer Ag | Kontinuierliche spinnverfahren fuer acrylnitrilfaeden und -fasern mit daempfung des spinngutes |
US4897990A (en) * | 1987-08-25 | 1990-02-06 | Mitsubishi Rayon Co | Highly shrinkable substantially acrylic filament yarn |
DE3832872A1 (de) * | 1988-09-28 | 1990-04-05 | Bayer Ag | Trockenspinnverfahren mit heissluft bei spinnschachtleistungen groesser 20 kg pro schacht und stunde |
DE3832870A1 (de) * | 1988-09-28 | 1990-03-29 | Bayer Ag | (kontinuierliche) herstellung von acrylnitrilfaeden und -fasern aus restloesungsmittelarmem spinngut |
US7771638B2 (en) * | 2007-12-19 | 2010-08-10 | E. I. Du Pont De Nemours And Company | Rapid plasticization of quenched yarns |
US7771637B2 (en) | 2007-12-19 | 2010-08-10 | E. I. Du Pont De Nemours And Company | High-speed meta-aramid fiber production |
US7771636B2 (en) * | 2007-12-19 | 2010-08-10 | E. I. Du Pont De Nemours And Company | Single stage drawing for MPD-I yarn |
CN115182063B (zh) * | 2021-04-01 | 2024-04-30 | 中国石油天然气股份有限公司 | 超高缩腈纶及其生产方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2417294A (en) * | 1944-02-25 | 1947-03-11 | Prophylactic Brush Co | Method of preparing molecularly oriented copolymerizates of acrylonitrile and other monoethylenic monomers |
US2811409A (en) * | 1952-12-31 | 1957-10-29 | Eastman Kodak Co | Spinning of acrylonitrile polymer fibers |
BE528051A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1953-06-25 | |||
FR1198455A (fr) * | 1957-01-18 | 1959-12-08 | Union Carbide Corp | Procédé de filage de polymères vinyliques |
US3097415A (en) * | 1959-02-20 | 1963-07-16 | Acrylonitrile fiber and process for | |
DE1494553A1 (de) * | 1965-03-02 | 1970-05-06 | Boehme Chem Fab Kg | Verfahren zur Herstellung von Fasern aus Polymeren oder Mischpolymeren des Acrylnitrils nach dem Trockenspinnverfahren |
US3739054A (en) * | 1971-04-05 | 1973-06-12 | Bayer Ag | Process for the production of high shrinkage threads yarns and fibersfrom acrylonitrile polymers |
DE2504079C2 (de) * | 1975-01-31 | 1984-03-29 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von hochschrumpffähigen, trockengesponnenen Acrylnitrilfasern oder -fäden |
US3991153A (en) * | 1975-06-24 | 1976-11-09 | American Cyanamid Company | Single phase extrusion of acrylic polymer and water |
DE2658179C2 (de) * | 1976-12-22 | 1983-02-03 | Bayer Ag, 5090 Leverkusen | Herstellung grobtitriger Acrylfasern |
DE2658916A1 (de) * | 1976-12-24 | 1978-07-06 | Bayer Ag | Polyacrylnitril-filamentgarne |
JPS5541329A (en) * | 1978-09-14 | 1980-03-24 | Toshiba Corp | Switching method of capacity of heating or cooling |
DE3010045A1 (de) * | 1980-03-15 | 1981-09-24 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von hochschrumpffaehigen reisszuegen aus acrylnitrilpolymerisation |
-
1982
- 1982-07-06 DE DE19823225268 patent/DE3225268A1/de active Granted
-
1983
- 1983-06-17 US US06/505,542 patent/US4508672A/en not_active Expired - Fee Related
- 1983-06-24 DE DE8383106188T patent/DE3369352D1/de not_active Expired
- 1983-06-24 EP EP83106188A patent/EP0098485B2/de not_active Expired - Lifetime
- 1983-07-05 JP JP58121120A patent/JPS5921713A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
DE3225268A1 (de) | 1984-01-12 |
DE3225268C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-11-08 |
EP0098485B1 (de) | 1987-01-21 |
DE3369352D1 (en) | 1987-02-26 |
EP0098485A2 (de) | 1984-01-18 |
US4508672A (en) | 1985-04-02 |
JPS5921713A (ja) | 1984-02-03 |
EP0098485A3 (en) | 1985-09-25 |
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