EP1841905A1 - Method for producing cellulose fiber - Google Patents
Method for producing cellulose fiberInfo
- Publication number
- EP1841905A1 EP1841905A1 EP05804903A EP05804903A EP1841905A1 EP 1841905 A1 EP1841905 A1 EP 1841905A1 EP 05804903 A EP05804903 A EP 05804903A EP 05804903 A EP05804903 A EP 05804903A EP 1841905 A1 EP1841905 A1 EP 1841905A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cellulose
- solution
- nmmo
- kneader
- powder
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 37
- 229920003043 Cellulose fiber Polymers 0.000 title claims description 18
- 239000001913 cellulose Substances 0.000 claims abstract description 152
- 229920002678 cellulose Polymers 0.000 claims abstract description 145
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 claims abstract description 120
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 71
- 230000008961 swelling Effects 0.000 claims abstract description 21
- 238000002156 mixing Methods 0.000 claims abstract description 14
- 238000004090 dissolution Methods 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 7
- 238000009987 spinning Methods 0.000 claims description 7
- 239000002861 polymer material Substances 0.000 claims description 4
- 238000005406 washing Methods 0.000 claims description 4
- 238000001125 extrusion Methods 0.000 claims description 2
- 238000004804 winding Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 42
- 230000008569 process Effects 0.000 abstract description 19
- 239000000835 fiber Substances 0.000 abstract description 13
- 238000007711 solidification Methods 0.000 abstract description 11
- 230000008023 solidification Effects 0.000 abstract description 11
- 239000012456 homogeneous solution Substances 0.000 abstract description 6
- 239000007788 liquid Substances 0.000 abstract description 3
- 235000010980 cellulose Nutrition 0.000 description 132
- 239000000243 solution Substances 0.000 description 106
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000002904 solvent Substances 0.000 description 10
- 239000002245 particle Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- 238000001816 cooling Methods 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 229920003124 powdered cellulose Polymers 0.000 description 7
- 235000019814 powdered cellulose Nutrition 0.000 description 7
- 239000002243 precursor Substances 0.000 description 7
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000010408 film Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 238000004220 aggregation Methods 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 241000157282 Aesculus Species 0.000 description 3
- -1 NMMO hydrates Chemical class 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000011552 falling film Substances 0.000 description 3
- 235000010181 horse chestnut Nutrition 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 101100165177 Caenorhabditis elegans bath-15 gene Proteins 0.000 description 2
- 229920000433 Lyocell Polymers 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 239000002025 wood fiber Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- ATSGLBOJGVTHHC-UHFFFAOYSA-N bis(ethane-1,2-diamine)copper(2+) Chemical compound [Cu+2].NCCN.NCCN ATSGLBOJGVTHHC-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 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
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D1/00—Treatment of filament-forming or like material
- D01D1/02—Preparation of spinning solutions
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/04—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres having existing or potential cohesive properties, e.g. natural fibres, prestretched or fibrillated artificial fibres
- D04H1/28—Regenerated cellulose series
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2201/00—Cellulose-based fibres, e.g. vegetable fibres
- D10B2201/20—Cellulose-derived artificial fibres
Definitions
- the present invention relates to a method for producing a cellulose solution which is homogeneous at low temperatures, and to fiber produced by the method. More particularly, the invention relates to a production of a cellulose solution which is homogeneous at low temperatures, by dissolving a small amount of the cellulose powder in concentrated liquid-state N-methylmorpholine-N-oxide (NMMO) to lower the solidification temperature of NMMO, introducing the low-temperature, concentrated liquid- state NMMO solution having cellulose dissolved and the cellulose powder into a kneader, mixing and swelling the cellulose in the kneader without a process of reducing pressure to produce a paste, and then supplying the paste into an extruder to dissolve the paste in a homogeneous solution.
- NMMO concentrated liquid-state N-methylmorpholine-N-oxide
- the fiber produced from the cellulose solution has excellent tenacity and dimensional stability, and thus can be usefully used for making a single fiber or a filament for clothing, as well as for making an industrial filament fiber or a reinforcing material for rubber products such as a tire and a belt.
- NMMO N-methylmorpholine-N-oxide
- U.S. Patent Nos. 3,447,935 discloses the process for production of cellulose fiber using the NMMO solvent.
- U.S. Patent Nos. 4,142,913, 4,144,080 disclose manufacturing methods for making cellulose solution by obtaining cellulose solution by under reduced pressure distillation of cellulose that is swelled and dispersed in NMMO hydrates, solidifying the cellulose solution to a precursor (solid-state) by cooling the cellulose solution(a kind if 'making chips' and melting in an extruder. These methods simplify the melting process by using an extruder, but require relatively long time and a large amount of energy because of the preceding 'making chips' And also, the precursor is hard to protect from heat and humidity.
- U.S. Patent No. 5,584,919 discloses a manufacturing method for making cellulose solution by preparing solid-state NMMO comprising 5 to 17% by weight water, feeding the solid-state NMMO with cellulose powder into a horizontal cylinder-type high speed mixer and mixing them to make a granule type precursor, and melting the precursor using an extruder.
- This method has a disadvantage of a wide distribution of the obtained the precursor and low yield. If the volume of the raw material is larger, the distribution of the obtained precursor is more widened. And a complicated cooling apparatus is required to transfer and store the precursor. And also, the solid-state NMMO is hard to manufacture and store.
- U.S. Patent Nos. 5,094,690, 5,534,113 and 5,603,883 disclose a manufacturing method for making cellulose solution by dispersing cellulose in the NMMO comprising 40% by weight water to make slurry, removing the water from the slurry by using a Force-drive type thin-layer distillation apparatus that can form a thin, solution-layer, and obtaining the cellulose solution.
- These methods have disadvantages of a low efficiency to the volume of the raw material because the slurry was distilled the water and melted by rotating of the rotor so slurry was downstreamed. It caused a short dwelling time in the above apparatus. And also, these methods require a relatively long time and relatively a large amount of energy to produce cellulose solution, and the obtained fiber using the above cellulose solution gets worse the tenacity by degradation of cellulose and change of color of the NMMO.
- U.S. Patent Nos. 5,421,525, 5,456,748, 5,534,113 and 5,888,288 disclose manufacturing methods cellulose solution by mixing pulp crashed into irregular flat type with NMMO comprising 22% by weight water in a horizontal cylinder-type mixer and swelling them, swelling again by stirring for hours in a storage hopper, removing the water form the high viscid solution by using a Force-drive type thin-layer distillation apparatus so as to obtain the melted cellulose solution.
- These methods have a disadvantage of extra handling and feeding of dust pulp produced as by-product during when crash the pulp into irregular flat type pulp. And also, it is hard to operate the horizontal cylinder-type mixer to discharge the swelled solution.
- U.S. Patent No. 5,921,675 discloses a horizontal cylinder-type mixer comprising a conveyor screw at the outlet of the mixer.
- U.S. Patent No. 5,948,905 discloses a manufacturing method for making cellulose solution by distilling the water from a mixture of cellulose and NMMO hydrates comprising about 23% by weight.
- the mixture was distilled under reduced pressure during passing the nozzle having 1.5 to 6.0millimeter diameter. It is composed of multi-stage chambers.
- the first-stage chamber has a small number of nozzles having relatively large diameter. As the chamber's stage is increased, the number of nozzle is increased and the diameter of the hole of the nozzle is decreased so as to increase the cross-sectional area in order to upgrade the efficiency of water vaporization.
- the last stage an extruder is used.
- This method however, has a disadvantage of needing of a highly complicated apparatus that is composed of many chambers different each other and comprised too many screws for shifting the chambers and distilling stages.
- PCT WO 1997/47790 discloses a manufacturing method for making cellulose solution by solving cellulose powder in the liquid-state NMMO directly in a twin- screw type extruder.
- the cellulose solution is produced by feeding the liquid-state NMMO comprising 12% by weight water into the first barrel of the extruder maintaining an inner temperature of 100°C, feeding cellulose powder into the third barrel of the extruder maintaining an inner temperature of 75°C, shifting and mixing them, and obtaining the solution by rising the temperature to 120°C.
- three barrel of the extruder is used for feeding the cellulose powder and NMMO, and another barrel is required for melting the cellulose.
- there is a relatively short swelling zone so as to obtain cellulose solution comprising undissolved cellulose particles.
- this method is effective to proceed relatively small amount of raw material, however, it is not proper to adapt a mass production of cellulose solution because there are too many undissolved moiety. And it is not proper economically because of requiring a lot of filter system. And also, this method has a disadvantage of too short spinning cycle. If the swelling zone of the extruder is increased by increasing the number of blocks and the L/D (length/diameter) of the screw, it is hard to control the swelling condition and the melting condition concurrently because the screws of the extruder are driven by single driving shaft.
- Korean patent application laid-open publication No. 2002-24689 discloses a manufacturing method for making highly homogenized cellulose solution by obtaining a mixture of swelled cellulose pulp powder and liquid-state NMMO by using the liquid- state NMMO that is overcooled by cooling air and melting the mixture.
- This method is hard to control the temperature of the overcooled NMMO by using the cooling air and to control the content of the NMMO because of exposing of the moisture contained in the cooling air.
- the prior arts provided manufacturing methods for making cellulose solution by contacting cellulose with NMMO containing 20 to 40% by weight water firstly, then, distilling the water by using a variety of distillation apparatus, followed by swelling and melting the cellulose.
- This method however, has a disadvantage of remaining undissolved moiety that caused by melting the cellulose immediately without swelling when the cellulose contacts with the NMMO maintaining at the temperature of 80°C(the crystallization temperature of NMMO) or more that has too high reaction activation.
- the present invention solves such conventional problems and, thus provides a ho- mogeneous cellulose solution even at low temperatures and a method for producing cellulose fiber from the cellulose solution.
- NMMO N-methyl- morpholine-N-oxide
- the invention is characterized in that when a kneader system is used, complete dissolution does not occur in the kneader, and a paste prepared by mixing and swelling the cellulose or by partially dissolving the cellulose is fed into an extruder, in which only the step of dissolution is carried out. Therefore, according to the invention, a large quantity of solution can be produced in a unit time, compared with the conventional method of using an extruder only, which is constituted of respective compartments for introducing raw materials employing NMMO of high concentration to dissolve cellulose, mixing, swelling, and dissolving.
- the method of the present invention is advantageous in that a simple mechanical apparatus is used, compared with the conventional method of using a complicated apparatus in which NMMO of low concentration is used to mix and swell cellulose, and then the cellulose is dissolved while the solvent is concentrated by removing water.
- the method for making a cellulose fiber from a homogeneous cellulose solution comprises the steps of (A) preparing an NMMO solution by dissolving a cellulose powder in concentrated liquid- state N-methylmorpholine-N-oxide (NMMO) to a small amount of 0.01 to 5% by weight; (B) introducing the NMMO solution having a small amount of the cellulose powder dissolved and the cellulose powder into a kneader, subsequently making a paste by mixing and swelling the cellulose in the kneader without reducing pressure, and then feeding the paste into an extruder; (C) spinning the cellulose solution by extrusion through a spinning nozzle, and then solidifying the spun cellulose solution which has passed through an air bed to reach a solidifying bath, to obtain a multifilament; and (D) washing, drying, oil-treating and winding the obtained multifilament.
- NMMO N-methylmorpholine-N-oxide
- the liquid-state NMMO having a small amount of cellulose dissolved may be maintained at a temperature of 50°C to 95°C in the step (A).
- the kneader into which the NMMO solution having the small amount of cellulose dissolved and the cellulose powder are introduced may be maintained at 50°C to 95°C in the step (B).
- the NMMO solution at the step (A) may contain moisture in an amount of 10 to 18% by weight of the total weight of the NMMO solution.
- the final cellulose solution may contain cellulose at a concentration of 5 to 20% by weight of the total weight of the cellulose solution.
- the liquid-state NMMO having a small amount of cellulose dissolved at the step (B) may be fed to the kneader while being maintained at a temperature of 50°C to 95°C.
- the cellulose powder at the step (A) or the step (B) may be mixed with other polymer materials.
- NMMO solution having a small amount of the cellulose powder dissolved in concentrated liquid-state NMMO
- the solidification temperature of the NMMO is lowered, and NMMO can be introduced and mixed in definite amounts at a low temperature, thereby rapid generation of film on the surface of the cellulose powder or powder lumps possibly being prevented.
- a homogeneous cellulose solution can be produced even at a low temperature, and upon spinning, a low temperature homogeneous cellulose solution can be used to inhibit the property of cellulose undergoing decomposition at high temperatures in the extruder, thus allowing production of cellulose molded articles having excellent flexibility and strength.
- Fig. 1 is a scheme briefly illustrating the process for producing a homogeneous cellulose solution by dissolving a small amount of the cellulose powder in NMMO of the invention
- Fig. 2 is a scheme illustrating the entire production process for according to the invention.
- Fig. 3 is a diagram showing the change behavior of the solidification temperature of
- Fig. 1 is a scheme briefly illustrating the procedure of the process for producing a homogeneous cellulose solution at a low temperature by dissolving a small amount of cellulose in NMMO according to an embodiment of the present invention.
- the cellulose powder used in Fig. 1 is obtained by pulverizing by means of a pulverizer equipped with a knife bar, and has a particle size of 5000 mm or less, and more specifically 500 mm or less.
- a pulverizer equipped with a knife bar When the size of the cellulose powder exceeds 5000 mm, it is difficult to uniformly disperse the cellulose powder, and thus there is a problem that the swelling process requires a long time.
- a small amount of the cellulose powder having a particle size of 5000 mm or less is first dissolved.
- the content of the cellulose powder is 0.01 to 5% by weight, and more specifically 0.1 to 3% by weight, with respect to the concentrated liquid- state NMMO.
- the content of the cellulose powder is less than 0.01% by weight, the effect of the cellulose powder on the lowering of the solidification temperature of NMMO is negligible, thus not contributing to the swellability.
- the content of the cellulose powder exceeds 5% by weight, the viscosity of the NMMO solution increases, thus the process of mixing and swelling in the kneader requiring a long time.
- the NMMO solution at a concentration of 20 to 30% by weight is concentrated by a conventional method to produce concentrated liquid-state NMMO having a water content of 10 to 18% by weight.
- the NMMO solution is concentrated to have a water content of less than 10% by weight, it is economically disadvantageous because of increased costs.
- the solubility of the cellulose powder may be deteriorated.
- the NMMO solution having a small amount of the cellulose powder dissolved is introduced into a kneader which has been maintained at 50 to 95°C.
- the cellulose is mixed and swelled in the kneader without reducing pressure, to form a paste, and then the paste is fed to an extruder, where the paste is dissolved to a homogeneous state to form a homogeneous cellulose solution.
- the NMMO solution having a small amount of the cellulose powder dissolved can be fed to the kneader by means of a gear pump or a screw type feeder, and is preferably introduced into the kneader by means of a screw type feeder.
- the content of the cellulose powder in the cellulose solution mixed and swelled in the kneader is adjusted to 5 to 20% by weight, and more specifically 9 to 14% by weight, with respect to the total weight of the liquid-state NMMO solution in accordance with the degree of polymerization of the cellulose polymer.
- the finally obtained fiber may not have the properties required from fiber.
- the content of the cellulose powder exceeds 20% by weight, it is difficult to dissolve the cellulose powder in the liquid-state NMMO, and thus a homogeneous solution cannot be obtained.
- cellulose is mixed and swelled in the kneader without a process of reducing pressure, to form a paste, and then the paste is fed to an extruder, where the paste is dissolved in a homogeneous state to produce a homogeneous solution.
- the extruder used for this purpose is preferably a twin-screw type extruder, and the twin- screw type extruder may have 3 to 16 barrels or may have the ratio L/D of the screw in the range of 12 to 64.
- the cellulose powder at the step (A) or step (B) may be mixed with other polymer materials or additives.
- a polymer material such as polyvinyl alcohol, polyethylene, polyethylene glycol, polymethyl methacrylate or a cellulose derivative, or an additive such as titanium dioxide, silicon dioxide, carbon or ammonium chloride may be mixed into the cellulose solution, in order to impart stability or spinnability to the cellulose solution, or to impart functionality to the final molded product.
- Fig. 2 is a scheme briefly illustrating the process of the invention for producing a highly homogeneous cellulose solution used for the production of lyocell, and the fiber.
- a pulp sheet 1 is conveyed by a nip roller 5 to a pulverizer 6.
- the pulp sheet 1 is passed through a drying chamber 2 adjusted to a constant temperature and then is cooled by dry air 3 to be maintained at 25°C.
- the dry temperature of the drying chamber 2 is controlled by a contact- type moisture content measuring device so that the moisture content may not exceed 7%.
- Commonly supplied pulp has a moisture content of about 8 to 10%.
- the moisture content of the powdered cellulose stored in a storage tank 10 after pulverization may vary depending on the seasonal changes in humidity and temperature. When the moisture content is high, aggregation of the pulp easily occurs, and it is difficult to obtain a homogeneous solution. In addition, there occurs variance in the composition of NMMO/cellulose/water, and there also occurs variance in the thickness of the fiber spun out through a nozzle 28, thus a uniform product not being obtained.
- the particle size of the powdered cellulose can be adjusted according to the size of the screen sieve disposed inside the pulverizer 6 equipped with a knife, and a powder having a size of 5000 mm or less, and more specifically, 500 mm or less, can be favorably used.
- the powdered cellulose passing through the screen sieve of the pulverizer 6 is supplied through a blower system 7 to a backfilter 8, while air is discharged out, with the powdered cellulose being fed to a powdered cellulose storage tank 10 through a rotary valve 9.
- the powdered cellulose is fed into a kneader 25 through a precise weight metering device 11.
- the used NMMO that is generated during the process is controlled at a concentration of 20 to 35% by weight in control bath 15 and fed to a purification column 17, where ionic materials, carbide impurities and the like are removed, and the purified NMMO is stored in the supply tank 18 of a concentration column.
- the NMMO is supplied in definite amounts from the supply tank of the concentration column sequentially to three falling film concentration columns 19, and is produced into an aqueous solution of NMMO at a final concentration of 86 to 88% by weight.
- the concentrated NMMO is fed to a jacketed storage tank 20 which is maintained at 95°C, and the liquid-state NMMO 20 and the cellulose powder 21 are metered to a dissolution tank 22 equipped with a combination mixer for high viscosity dissolution, in order to be produced into an NMMO solution having a small amount of 0.01 to 5% by weight of cellulose powder dissolved.
- the produced solution is transported to a solution base tank 23, and is supplied in definite amounts together with the cellulose powder 11 into the kneader 25 through a gear pump 24.
- the kneader 25 which is maintained at a desired temperature by heat medium jacketing can be adjusted to a temperature of about 50 to 95°C, and the suitable temperature may vary depending on the concentration of the cellulose dissolved in the introduced NMMO, the molecular weight of the cellulose powder used, and the final cellulose concentration.
- NMMO When the low-temperature NMMO in which a small amount of cellulose is dissolved and the cellulose powder are mixed and kneaded in the kneader at 50 to 95°C, NMMO penetrates uniformly to the entire area of the cellulose, thereby forming a paste. As the paste is transported forward, the paste makes cellulose to swell and starts to partially dissolve the cellulose. The paste is supplied to a twin screw extruder 26 through a forced transporting device 12. The internal temperature of the twin-screw type extruder is adjusted in the range of 60°C to 105°C, and the cellulose in the paste is completely dissolved under the effects of the temperature increase and the shear force.
- the obtained cellulose solution passes through a filter 27 and then is spun through a nozzle 28, and the spun cellulose is solidified in solidifying bath 13, washed in washing bath 14, and then finally dried to be produced into a cellulose fiber in dryer 29.
- a concentration of the used NMMO that is generated during the solidifying and washing process is controlled in control bath 15, and then the controlled NMMO is fed to the solidifying bath 13 by pump 16.
- Fig. 3 is a diagram illustrating the change behavior of the solidification temperature of NMMO in accordance with the cellulose concentration. Referring to Fig. 3, it can be seen that even if a small amount (about 0.01 to 6%) of cellulose is dissolved, the solidification temperature of NMMO is remarkably lowered from 75°C to 30°C.
- a small amount of the cellulose powder is dissolved in concentrated liquid- state NMMO in order to lower the solidification temperature of the NMMO solution.
- the NMMO solution can be fed to the kneader in the liquid state at a relatively low temperature.
- the process can be carried out in a wide range of temperature, and also, the cellulose powder and the NMMO solution can be easily mixed and swelled at a low temperature. This prevents generation of film on the surface of the cellulose powder, and eventually, a cellulose solution which is homogeneous even at low temperatures can be produced.
- a sample of the cellulose solution produced according to the invention was taken from the solution transport line immediately after passing through a kneader and being discharged from a twin-screw type extruder and was subjected to eye observation with a polarized microscope, and then the solubility of the cellulose solution was evaluated.
- the extent of the dissolved state was classified into 5 grades.
- the completely dissolved state was rated as Grade T, while an unspinnable state where a large quantity of undissolved components were present was rated as Grade '5'.
- the intermediate grades were classified into Grades 2, 3 and 4 in accordance with the amount of residual undissolved cellulose.
- a cellulose sheet having a weight average degree of polymerization of 1,200 (V-81 available from Buckeye Technologies) was dried in a drying chamber to have a moisture content of 6.5 to 10%.
- a cellulose powder having a particle size of 500 mm or less and a moisture content of 3.5 to 7% by weight was produced using a pulverizer equipped with a screen sieve having a mesh size of 500 mm, and liquid-state NMMO concentrated to 87.5% by weight in a falling film concentration column and maintained at 90°C was produced.
- liquid-state NMMO concentrated to 87.5% by weight in a falling film concentration column and maintained at 90°C was produced.
- 0.001% by weight, with respect to the concentrated liquid-state NMMO of an antioxidant was added and dissolved.
- the liquid-state NMMO and the cellulose powder were metered into a dissolution tank equipped with a combination mixer for high viscosity dissolution, and a NMMO solution having cellulose powder dissolved to a small amount of 0.01 to 2.5% by weight was produced.
- the produced NMMO solution was introduced in definite amounts to a kneader whose internal temperature was maintained at 50 to 95°C, by means of a gear pump.
- the cellulose powder was metered by a precise weight metering device (K-tron feeder) and was introduced to the kneader, so that the final concentration of the cellulose paste was 11% by weight of the total solution.
- the kneader used herein had a volume of about 30 L, and the speed of the rotating blade was 20 to 30 rpm.
- the produced paste was transported by force to be fed into a co- rotating twin-screw type extruder.
- the twin-screw type extruder used had a screw with a diameter of 47 mm ⁇ and the barrel temperature at the initial feeding section was maintained at 60 to 70°C, while the barrel temperature at the final discharge section was maintained at 95 to 105°C.
- the produced paste was swelled and dissolved, and was fed to a nozzle through a gear pump after passing through a filter.
- sampling was done from the solution transport line immediately after discharge from the twin-screw type extruder.
- the cellulose solution was discharged through a nozzle having 1,000 orifices, in which the orifice diameter was 150 mm, and the orifices's interval was 1.5 mm.
- the length of the air bed was maintained to be 90 mm, and the temperature and relative humidity of the cooling air blown from the air bed to the filament were 25°C and 45% RH, respectively.
- the blowing speed was adjusted to 6.5 m/sec.
- the filament entering a solidifying bath from the air bed was washed, dried, oil-treated and then wound. The fineness of the finally obtained multi-filament was adjusted to 1500 deniers.
- a cellulose sheet having a weight average degree of polymerization of 850 (V-60 available from Buckeye Technologies) was dried in a drying chamber to have a moisture content of 6.5 to 10%.
- a cellulose powder having a particle size of 500 mm or less and a moisture content of 3.5 to 7% by weight was produced using a pulverizer equipped with a screen sieve having a mesh size of 500 mm, and liquid-state NMMO concentrated to 87.5% by weight in a falling film concentration column and maintained at 85°C was produced.
- liquid-state NMMO concentrated to 87.5% by weight in a falling film concentration column and maintained at 85°C was produced.
- 0.001% by weight, with respect to the concentrated liquid-state NMMO of an antioxidant was added and dissolved.
- the liquid-state NMMO and the cellulose powder were metered into a dissolution tank equipped with a combination mixer for high viscosity dissolution, and a NMMO solution having cellulose powder dissolved to a small amount of 0.1 to 5% by weight was produced.
- the produced NMMO solution was introduced in definite amounts to a kneader whose internal temperature was maintained at 50 to 95°C, by means of a gear pump.
- the cellulose powder was metered by a precise weight metering device and was introduced to the kneader, so that the final concentration of the cellulose paste was 13% by weight of the total solution.
- the kneader used herein had a volume of about 30 L, and the speed of the rotating blade was 20 to 30 rpm.
- the produced paste was transported by force to be fed into a co-rotating twin-screw type extruder.
- the twin- screw type extruder used had a screw with a diameter of 47 mm ⁇ and the barrel temperature at the initial feeding section was maintained at 50 to 70°C, while the barrel temperature at the final discharge section was maintained at 95 to 105°C.
- the produced paste was swelled and dissolved, and was fed to a nozzle through a gear pump after passing through a filter.
- sampling was done from the solution transport line immediately after discharge from the twin-screw type extruder.
- the cellulose solution was discharged through a nozzle having 50 orifices, in which the orifice diameter was 150 mm, and the orifices's interval was 2.5 mm.
- the length of the air bed was maintained to be 60 mm, and the temperature and relative humidity of the cooling air blown from the air bed to the filament were 23°C and 55% RH, respectively.
- the blowing speed was adjusted to 7 m/sec.
- the filament entering a solidifying bath from the air bed was washed, dried, oil-treated and then wound. The fineness of the finally obtained multi-filament was adjusted to 50 to 100 deniers.
- Example 22 a multi-filament was produced by the same method as that used in
- cellulose is pulverized by controlling the moisture content of a pulp sheet, and a small amount of the cellulose powder is dissolved in concentrated liquid- state NMMO to lower the solidification temperature of the NMMO.
- an NMMO solution can be fed to a kneader at a relatively low temperature, and the cellulose powder and the NMMO solution can be easily mixed and swelled in the kneader at low temperatures.
- NMMO solution When only a high-temperature NMMO solution is used, rapid swelling and dissolving at the surface of the cellulose powder or powder lumps may occur during the initial mixing and swelling process, and thus aggregation of the cellulose powder may occur.
- a homogeneous cellulose solution can be produced even at a low temperature, and upon spinning, a low temperature homogeneous cellulose solution can be used to inhibit the property of cellulose undergoing decomposition at high temperatures in the extruder, thus allowing production of cellulose molded articles having excellent flexibility and strength.
- pulp having low specific gravity can be easily introduced into a kneader having a high internal space as suggested in the present invention, and thus the output of the solution and the output of the cellulose molded articles can be increased.
- direct introduction of concentrated NMMO at a concentration of about 86.5% by weight eliminates the need for a separate water evaporating unit utilizing reduced pressure, thus simplifying the structure of the apparatus.
- the filter exchange interval is shortened. Furthermore, a cellulose paste which has been preliminarily swelled is produced in the kneader and fed to a twin-screw type extruder in a state having the minimum volume, and thus screw arrangement inside the twin-screw type extruder is less stressful.
- insertion of reverse screw elements or kneading discs can be minimized, and thus the residence time distribution for the cellulose solution in the extruder may be made narrow, thus decomposition of the cellulose being prevented.
- the use of a twin-screw type extruder having high shear force efficiency immediately after the kneader allows reduction of the dissolution time and dissolution temperature, and since reduction of the original degree of polymerization of pulp is minimized, the high molecular weight can be maintained.
- a cellulose fiber having excellent properties can be produced by the method according to the present invention.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020040116907A KR100575388B1 (en) | 2004-12-30 | 2004-12-30 | A highly homogeneous cellulose solution and fiber produced by using the same |
PCT/KR2005/004677 WO2006071101A1 (en) | 2004-12-30 | 2005-12-30 | Method for producing cellulose fiber |
Publications (3)
Publication Number | Publication Date |
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EP1841905A1 true EP1841905A1 (en) | 2007-10-10 |
EP1841905A4 EP1841905A4 (en) | 2009-08-19 |
EP1841905B1 EP1841905B1 (en) | 2010-09-29 |
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EP05804903A Not-in-force EP1841905B1 (en) | 2004-12-30 | 2005-12-30 | Method for producing cellulose fiber |
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US (1) | US20080054516A1 (en) |
EP (1) | EP1841905B1 (en) |
JP (1) | JP4210285B2 (en) |
KR (1) | KR100575388B1 (en) |
CN (1) | CN100354461C (en) |
AT (1) | ATE483044T1 (en) |
DE (1) | DE602005023907D1 (en) |
RU (1) | RU2362845C2 (en) |
TW (1) | TW200626617A (en) |
WO (1) | WO2006071101A1 (en) |
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WO2015101543A1 (en) | 2014-01-03 | 2015-07-09 | Lenzing Aktiengesellschaft | Cellulose fiber |
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JPWO2022145275A1 (en) * | 2021-01-04 | 2022-07-07 | ||
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EP4219567A1 (en) | 2022-01-31 | 2023-08-02 | LIST Technology AG | Assembly and method for processing a starting material into a forming solution by means of a dry dissolving process |
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CN115182096B (en) * | 2022-05-27 | 2024-03-22 | 杭州诺邦无纺股份有限公司 | Cellulose filament non-woven material and preparation method thereof |
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- 2005-12-27 JP JP2005374370A patent/JP4210285B2/en not_active Expired - Fee Related
- 2005-12-30 AT AT05804903T patent/ATE483044T1/en active
- 2005-12-30 US US10/565,098 patent/US20080054516A1/en not_active Abandoned
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US10883196B2 (en) | 2014-01-03 | 2021-01-05 | Lenzing Aktiengesellschaft | Cellulose fiber |
Also Published As
Publication number | Publication date |
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US20080054516A1 (en) | 2008-03-06 |
WO2006071101A1 (en) | 2006-07-06 |
KR100575388B1 (en) | 2006-05-03 |
CN100354461C (en) | 2007-12-12 |
EP1841905A4 (en) | 2009-08-19 |
TWI310386B (en) | 2009-06-01 |
DE602005023907D1 (en) | 2010-11-11 |
EP1841905B1 (en) | 2010-09-29 |
JP2006188806A (en) | 2006-07-20 |
CN1796624A (en) | 2006-07-05 |
RU2362845C2 (en) | 2009-07-27 |
TW200626617A (en) | 2006-08-01 |
RU2007124513A (en) | 2009-02-10 |
JP4210285B2 (en) | 2009-01-14 |
ATE483044T1 (en) | 2010-10-15 |
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