WO2003014437A1 - High-strength polyethylene fiber - Google Patents
High-strength polyethylene fiber Download PDFInfo
- Publication number
- WO2003014437A1 WO2003014437A1 PCT/JP2002/007910 JP0207910W WO03014437A1 WO 2003014437 A1 WO2003014437 A1 WO 2003014437A1 JP 0207910 W JP0207910 W JP 0207910W WO 03014437 A1 WO03014437 A1 WO 03014437A1
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- WO
- WIPO (PCT)
- Prior art keywords
- fiber
- molecular weight
- average molecular
- strength
- weight
- Prior art date
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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
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
-
- 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
- D01D10/00—Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
- D01D10/02—Heat treatment
-
- 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
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/08—Melt spinning methods
- D01D5/098—Melt spinning methods with simultaneous stretching
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/02—Yarns or threads characterised by the material or by the materials from which they are made
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/32—Elastic yarns or threads ; Production of plied or cored yarns, one of which is elastic
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/44—Yarns or threads characterised by the purpose for which they are designed
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- 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
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/02—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
- D10B2321/021—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins polyethylene
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- 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
- D10B2401/00—Physical properties
- D10B2401/06—Load-responsive characteristics
- D10B2401/061—Load-responsive characteristics elastic
-
- 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
- D10B2401/00—Physical properties
- D10B2401/06—Load-responsive characteristics
- D10B2401/063—Load-responsive characteristics high strength
-
- 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
- D10B2501/00—Wearing apparel
-
- 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
- D10B2507/00—Sport; Military
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
Definitions
- the present invention relates to high-performance textile styles such as various sports clothing, bulletproof, protective clothing, protective gloves and various safety articles, tag ropes, mooring ropes, boat ropes, architectural ropes, and the like.
- Various rope products, various braid products such as fishing lines and blind cables, net products such as fishing nets and ballistic nets, as well as chemical filters and electronics
- Theta-curtain materials such as reinforcing materials or tents for various nonwoven fabrics, or for sports such as helmets or skis-for copiers such as speaker cones and pre-preda
- the present invention relates to a new high-strength polystyrene fiber that can be applied to a wide range of industries as a reinforcing fiber for composites and a reinforcing fiber for concrete.
- ultra-high molecular weight polyethylene is used as a raw material, and the so-called "gel spinning method” is used to achieve the conventional V, high strength and high strength. It is known that elastic modulus fibers can be obtained and is already widely used in industry.
- US Pat. No. 4,222,118 discloses an r3 ⁇ 4 strength polystyrene fiber produced by melt spinning.
- a high-strength polyethylene fiber of 6 c NZ dtex or higher is disclosed.
- Japanese Patent Application Laid-Open Publication No. Hei 8-540981 discloses that a high-density polyethylene is melt-spun through a spinneret and the fiber exits from the spinneret.
- a high-strength polystyrene fiber produced by cooling an obtained fiber and stretching the obtained fiber at 50 to 150 C is disclosed.
- the high-strength polyethylene fiber Since the invention of the high-strength polyethylene fiber by gel spinning, the high-strength polyethylene fiber has been used in all fields, and the high-strength polyethylene fiber as the raw yarn has been used.
- the physical properties required of len fibers have been increasing in recent years.
- the mechanical strength and elastic modulus are excellent at all single fiber deniers, the fibers are uniform, and At the same time, it is necessary to satisfy that there is no fusion between fibers.
- high-strength polyethylene fibers with a small single-filament fineness are required.
- ropes and nets which are problematic in terms of fluff, slippage, so-called abrasion resistance, etc., it is preferable that the single yarn fineness is somewhat thicker.
- high-strength polyethylene fibers Accordingly, attempts have been made to produce high-strength polyethylene fibers by so-called melt spinning, high-strength polyethylene fibers satisfying all of the above performances have not yet been obtained. is there.
- high-strength polyethylene fibers can be obtained by using gel spinning, but high-strength polystyrene fibers with low single-filament fineness obtained by gel spinning can be obtained.
- There are many fusion and crimping between single fibers In particular, when the fibers are used for a thin-walled nonwoven fabric, the fused / compressed fibers become uneven in thickness, causing a defect, and the physical properties of the nonwoven fabric are deteriorated. In addition, there was a problem that the knot strength and the loop strength retention were reduced due to the fact that the fiber diameter was increased by the fused and crimped fiber.
- the weight average molecular weight in the fiber state is 300,000 or less, the ratio of the weight average molecular weight to the number average molecular weight (MwZMn) is 4.0 or less, and the main chain is 100,000 carbon atoms. 0.01 to 3.0 per minute
- a high-strength polyethylene fiber characterized by having a strength of polystyrene containing a branched chain of 15 c NZ dtex or more.
- the modulus of elasticity is 500 cNZ dtex or more
- the cut fiber is used, the poorly dispersed yarn is used.
- the present invention also provides a high-strength polyethylene fiber having a ratio of 2.0% or less.
- the method for producing the fiber according to the present invention requires a careful and novel production method.
- the following method is recommended, but is not limited thereto.
- Polyethylene in the present invention is characterized in that its repeating unit is practically ethylene, and a small amount of other mono- or mono-olefins is used. Copolymerized.
- ⁇ -olefins allows the fibers to contain some long-chain branching, which gives the fibers the following characteristics. That is, the present inventors surprisingly possessed a certain degree of branching in the main chain, and improved the crimping caused by the pressure applied when the fiber was cut. I found that. The detailed reason is not clear, but for example, it is speculated as follows. High-strength polyethylene fibers are difficult to cut essentially because the molecular chains are highly oriented and crystallized in the fiber axis direction.
- an alkyl group having 5 or more carbon atoms per 100 main carbon atoms is branched at a ratio of 0.01 to 3 carbon atoms per 100 main carbon atoms. It is more preferably 0.05 to 2 per 100 carbons of the main chain, and more preferably 0.1 to 1 per carbon.
- the weight average molecular weight in the fiber state is 300,000 or less, and that the ratio (MwZMn) of the weight average molecular weight to the number average molecular weight is 4.0 or less.
- the weight average molecular weight in the fibrous state is not more than 250.000, and the ratio (Mw / Mn) of the weight average molecular weight to the number average molecular weight is not more than 3.5. This is very important. More preferably, the weight average molecular weight in the fibrous state is 200,000 or less, and the ratio of the weight average molecular weight to the number average molecular weight (MwZMn) is 3.0 or less. And are important.
- the raw material is a polystyrene having a polymerization degree such that the weight average molecular weight of the polystyrene in a fibrous state exceeds 300,000, the melt viscosity is extremely high. As a result, melt molding becomes extremely difficult. Also, when the ratio of the weight average molecular weight to the number average molecular weight in the fiber state is 4.0 or more, the maximum draw ratio is lower than when a polymer having the same weight average molecular weight is used, and the obtained yarn is obtained. Is low in strength. This is because, when compared with the same weight-average polyethylene, the molecular chain having a long relaxation time cannot be extended during stretching, causing a break.
- the polymer in order to control the molecular weight and molecular weight distribution in the fiber state, the polymer may be deliberately degraded in the dissolving / extrusion process or the spinning process, or the molecular weight may be narrow in advance.
- Polyethylene with distribution may be used. In the production method recommended by the present invention, such a polyethylene is extruded by an extruder, melted and extruded, and is discharged quantitatively through a spinneret by a gear pump. Thereafter, the filament is cooled with cold air, and is taken out at a predetermined speed. In this case, it is important to take off quickly enough. That is, the ratio between the discharge linear speed and the winding speed is
- the ratio between the discharge linear speed and the winding speed can be calculated from the die diameter, the single hole discharge amount, the polymer density in the molten state, and the winding speed.
- gel spinning does not use a solvent, for example, when a round die is used, the cross section of the fiber becomes a round shape, and even when the spinning and drawing are performed under tension. Crimping is unlikely to occur.
- the fiber be drawn by the following method in addition to the above spinning conditions.
- the fiber is drawn at a temperature equal to or lower than the crystal dispersion temperature of the fiber, specifically, at 65 ° C or lower, and at a temperature equal to or higher than the crystal dispersion temperature of the fiber and equal to or lower than the melting point, specifically, 90 ° C.
- the physical properties of the fiber are surprisingly improved by further stretching.
- the fiber may be further extended in multiple stages.
- the speed of the first godet roll is fixed at SmZmin, and the speed of the other godet rolls is changed.
- a yarn having a predetermined draw ratio was obtained.
- the strength and elastic modulus in the present invention were measured using a sample made by Orientec, "Tensilon", with a sample length of 200 mm (length between chucks) and elongation. Measure the strain-stress curve under the condition of 100% of long speed and 100% of the ambient temperature and the relative humidity of 65%, and measure the stress at the break point of the curve with the strength (c NZ dtex) and the curve. The elastic modulus (cNdtex) was calculated from the tangent that gives the maximum gradient near the origin. The average value of 10 measurements was used for each value.
- the weight-average molecular weight Mw, number-average molecular weight Mn and Mw / Mn are gels.
- the measurement was performed by a chromatograph (GPC). GPC device made by 1 ⁇ & 65 0? The test was carried out using a GPCUT 802.5 made by SHODEX and two UTs 806M as columns.
- the measurement solvent used was 0-dichlorobenzene, and the column temperature was set at 144 ° C.
- the sample concentration was set to 1.0 mg Zm1, and 200 microliters were injected for measurement.
- the calibration curve of the molecular weight is constructed by using a polystyrene sample with a known molecular weight by the universal calibration method.
- the dynamic viscosity measurement in the present invention was carried out using “Leonoku Ibron DDV-01 FP type” manufactured by Orientec.
- the fibers are split or tied to give a total of 100 denier ⁇ 10 denier, and the measurement length is taken into consideration so that each single fiber is arranged as uniformly as possible. Wrap both ends of the fiber with aluminum foil so that the distance between the scissors metal fittings is 20 mm, and bond with a cellulose adhesive. I do. In this case, the length of the glue margin should be about 5 mm in consideration of fixing to the scissors.
- Each test piece was carefully placed on scissors (chucks) set to an initial width of 20 mm so that the thread would not be loosened or twisted.
- This experiment was performed after preliminarily deforming for several seconds at a frequency of 110 Hz.
- the temperature dispersion at a frequency of 110 Hz was obtained from the lower temperature side at a heating rate of about 1 in the temperature range from 150 ° C to 150 r.
- the static load was set to 5 gf, and the o-P was automatically adjusted5 so that the fiber did not loosen.
- the dynamic deformation amplitude was set to 15 m
- Weight-average molecular weight 11.5, 000, ratio of weight-average molecular weight to number-average molecular weight is 2.3, and branched chains with a length of 5 or more carbons per 100,000 carbons.
- Four high-density polyethylenes were fed from a spinneret consisting of ⁇ 23 ⁇ 4 0.8 mm, 30 H at 290 ° C at a single-hole discharge rate of 0.5 g / min. Extruded. The extruded fiber passes through a heat insulation section of 15 cm, is cooled by a 20 ° (: 0.5 m / s) quench, and is wound at a speed of SOO mZmin.
- the undrawn yarn was drawn by a Nelson roll capable of controlling the temperature of multiple units, and the single-stage drawing was performed 2.8 times at 25 ° C. It was heated to ° C and stretched 5.0 times to obtain a drawn yarn.
- the physical properties of the obtained fiber are shown in Table 1.
- Example 2 The drawn yarn of Example 1 was heated to 125 ° C. and further drawn 1.3 times. Table 1 shows the physical properties of the obtained fiber.
- a drawn yarn was prepared under the same conditions as in Example 1 except that the drawing temperature of the first stage was set at 40 ° C. Table 1 shows the physical properties of the obtained fiber.
- a drawn yarn was prepared under the same conditions as in Example 1 except that the drawing temperature of the first step was set at 10 ° C. Table 1 shows the physical properties of the obtained fiber.
- Weight average molecular weight 152, 000, ratio of weight average molecular weight to number average molecular weight: 2.4, branched chains with a length of 5 or more carbons per 1,000 carbon atoms: 0.
- Four high-density polyethylenes were extruded from a ⁇ 0.9 mm, 30 H spinneret at 300 ° C at a single hole discharge rate of 0.S g Zmin. Except for the above, a drawn yarn was obtained in the same manner as in Example 1.
- Table 1 shows the physical properties of the obtained fiber.
- Four high-density polyethylenes are extruded at a speed of 0.8 g Zmin with a single hole discharge rate of 300 mm from a spinneret consisting of 0.1 mm and 30 H. did.
- the extruded fiber passes through a heat insulation section of 15 cm, is cooled by a 20 ° (: 0.5 mZs) quench, and is wound up at a speed of ISO mZmin.
- the yarn was stretched by a plurality of nelson rolls capable of controlling the temperature, and the single-stage stretching was performed at a temperature of 25 ° C by a factor of 2.0. Then heat it to 115 ° C and increase it by 4.0 times. Drawing was performed to obtain a drawn yarn. Table 1 shows the physical properties of the obtained fiber.
- a drawn yarn was prepared under the same conditions as in Example 1 except that the drawing temperature in the first step was 90 ° C.
- Table 2 shows the physical properties of the obtained fiber.
- Example 2 shows the physical properties of the obtained fiber.
- Example 2 shows the physical properties of the obtained fiber.
- a drawn yarn was prepared under the same conditions as in Example 1 except that high-density polystyrene was used.However, yarn breakage frequently occurred during drawing, and only a drawn yarn with a low draw ratio was obtained. Was. Table 2 shows the physical properties of the obtained fiber.
- Four high-density polyethylenes were extruded at a speed of 0.5 g Zmin with a single hole discharge rate of 270 from a spinneret consisting of ⁇ Q .8 mm, 30 H force. Except for An undrawn yarn was prepared in the same manner as in Example 1. The undrawn yarn was drawn 2.8 times at 90 ° C. Then, it was heated to 115 ° C and stretched 3.8 times to obtain a drawn yarn. Table 2 shows the physical properties of the obtained fiber.
- Comparative Example 7 The undrawn yarn obtained in Comparative Example 4 was drawn 2.8 times at 40 ° C. Then, it was heated to 115 ° C and stretched 4.0 times to obtain a stretched yarn. Table 2 shows the physical properties of the obtained fiber. (Comparative Example 7)
- An undrawn yarn was prepared in the same manner as in Comparative Example 4, except that the spinning speed was 80 mm inn.
- the undrawn yarn was drawn 2.8 times at 80 ° C. Then, it was heated to 115 ° C and stretched 4.0 times to obtain a drawn yarn.
- Table 3 shows the physical properties of the obtained fiber.
- Weight average molecular weight 123, 000, ratio of weight average molecular weight to number average molecular weight 6.0, 0 branched carbon chains with a length of 5 or more carbons per 100,000 carbons Extruded from a spinneret consisting of 0.8 mm, 30 H at 295 ° C at a single-hole discharge rate of 0.5 g / min. Produced an undrawn yarn in the same manner as in Example 1. The undrawn yarn was drawn 2.8 times at 90 ° C. Then, it was heated to 115 ° C and stretched 3.7 times to obtain a drawn yarn. Table 3 shows the physical properties of the obtained fiber.
- 6 high-density polyethylenes were fed through a spinneret consisting of 0.8 mm, 30 H
- An undrawn yarn was prepared in the same manner as in Example 1 except that the single hole ejection amount was extruded at a speed of 0.5 g Zmin.
- the undrawn yarn was drawn 2.8 times at 40 ° C. Then, it was heated to 100 ° C. and stretched 5.0 times to obtain a drawn yarn.
- Table 3 shows the physical properties of the obtained fiber.
- Weight average molecular weight 8,200,000, ratio of weight average molecular weight to number average molecular weight: 2.5, length of branches with 5 or more carbons: 1.3 per 1,000 carbons
- Ultra-high molecular weight polyethylene having a weight-average molecular weight of 3,200,000 and a ratio of weight-average molecular weight to number-average molecular weight of 6.3 was added at 1 O wt% and decahydronuff. Disperse a 90 wt% slurry-like mixture in a screw-type kneader set at a temperature of 230 ° C while dispersing, and bring the mixture to 170 ° C. A set hole having a diameter of 0.2 mm and a hole having 200 holes was supplied by a metering pump at a single hole discharge rate of 0.08 g Zmin.
- the slit gas supply orifice installed directly under the nozzle applies nitrogen gas adjusted to 100 ° C at a speed of 1.2 m / min as evenly as possible on the yarn.
- the decalin on the fiber surface is actively evaporated, and immediately thereafter, it is substantially cooled by an air flow set at 30 ° C., and the nesol installed downstream of the nozzle It was pulled off at a speed of 50 mZ by a roller in the shape of a thread. At this time, the solvent contained in the thread was reduced to about half of the original weight.
- the obtained fiber was stretched three times in a heating oven at 100 degrees, and then continuously 4.6 times in a heating oven set at 149 degrees. Stretched. Uniform fibers could be obtained without breaking during the process. Table 3 shows the physical properties of the obtained fiber.
- the slurry mixture adjusted in the same manner as in Comparative Example 10 was melted with a screw-type kneader set at a temperature of 230 ° C, and the diameter was set at 180 ° C. .8 mm was fed to a base having 500 holes at a single hole discharge rate of 1.6 gmin using a metering pump.
- a slit-shaped gas supply orifice installed directly below the nozzle applies nitrogen gas adjusted to 100 ° C at a rate of 1.2 m / min as evenly as possible on the yarn.
- the decalin on the fiber surface was aggressively evaporated, and then at a speed of 10 Om / min by a nerson-shaped roller installed downstream of the nozzle At this time, the solvent contained in the form of a thread was reduced to about 60% of its original weight. Subsequently, the obtained fiber was stretched 4.0 times in a heating oven at 130 degrees, and the fiber was then stretched 3.5 times in a heating oven installed at 149 degrees. Stretched. A uniform fiber was obtained without breaking during the process. Table 3 shows the physical properties of the obtained fiber.
- Example 2 Example 3
- Example 4 Example 5
- Example 6 Weight average molecular weight g / mo I 11500 11500 11500 12300 12150 12150
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Artificial Filaments (AREA)
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE60228115T DE60228115D1 (de) | 2001-08-08 | 2002-08-02 | Hochfeste polyethylenfaser |
EP02753220A EP1445356B1 (en) | 2001-08-08 | 2002-08-02 | High-strength polyethylene fiber |
KR1020047001868A KR100909559B1 (ko) | 2001-08-08 | 2002-08-02 | 고강도 폴리에틸렌 섬유 |
US10/486,110 US7056579B2 (en) | 2001-08-08 | 2002-08-02 | High-strength polyethylene fiber |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001241118A JP4389142B2 (ja) | 2001-08-08 | 2001-08-08 | 高強度ポリエチレン繊維の製造方法 |
JP2001-241118 | 2001-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003014437A1 true WO2003014437A1 (en) | 2003-02-20 |
Family
ID=19071622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2002/007910 WO2003014437A1 (en) | 2001-08-08 | 2002-08-02 | High-strength polyethylene fiber |
Country Status (8)
Country | Link |
---|---|
US (1) | US7056579B2 (ja) |
EP (1) | EP1445356B1 (ja) |
JP (1) | JP4389142B2 (ja) |
KR (2) | KR100951222B1 (ja) |
CN (1) | CN1271257C (ja) |
AT (1) | ATE403766T1 (ja) |
DE (1) | DE60228115D1 (ja) |
WO (1) | WO2003014437A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1493851A4 (en) * | 2002-04-09 | 2006-10-04 | Toyo Boseki | POLYETHYLENE FIBER AND THEIR PRODUCTION PROCESS |
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US20060049056A1 (en) * | 2002-04-12 | 2006-03-09 | Acm Research, Inc. | Electropolishing and electroplating methods |
JP2007277763A (ja) * | 2006-04-07 | 2007-10-25 | Toyobo Co Ltd | 高強度ポリエチレン繊維 |
CN101230501B (zh) * | 2008-02-26 | 2010-06-02 | 山东爱地高分子材料有限公司 | 一种采用超高分子量聚乙烯与低密度聚乙烯共混熔融制备高强聚乙烯纤维的方法 |
EP2316990B1 (en) * | 2008-08-20 | 2013-01-16 | Toyobo Co., Ltd. | Highly functional polyethylene fiber, woven/knitted fabric comprising same, and glove thereof |
JP5664982B2 (ja) | 2009-08-04 | 2015-02-04 | ディーエスエム アイピー アセッツ ビー.ブイ. | 被覆高強度繊維 |
JP4816798B2 (ja) * | 2010-02-19 | 2011-11-16 | 東洋紡績株式会社 | 成型加工性に優れた高機能ポリエチレン繊維 |
WO2011135082A1 (en) | 2010-04-29 | 2011-11-03 | Dsm Ip Assets B.V. | Multifilament yarn construction |
US9687593B2 (en) | 2010-12-10 | 2017-06-27 | Dsm Ip Assets B.V. | HPPE member and method of making a HPPE member |
TWI397621B (zh) * | 2011-01-24 | 2013-06-01 | Toyo Boseki | 成型加工性優異的高機能聚乙烯纖維 |
EP2481847A1 (en) | 2011-01-31 | 2012-08-01 | DSM IP Assets B.V. | UV-Stabilized high strength fiber |
MY161188A (en) * | 2011-03-03 | 2017-04-14 | Toyo Boseki | Highly functional polyethylene fiber, and dyed highly functional polyethylene fiber |
JP6040584B2 (ja) * | 2012-06-15 | 2016-12-07 | 東洋紡株式会社 | ポリエチレン繊維からなるセメント系構造物補強用短繊維、およびセメント系構造物 |
KR20150110550A (ko) | 2013-01-25 | 2015-10-02 | 디에스엠 아이피 어셋츠 비.브이. | 연신된 멀티필라멘트 얀의 제조 방법 |
JP6582434B2 (ja) * | 2015-02-20 | 2019-10-02 | 東洋紡株式会社 | 組紐 |
JP6582433B2 (ja) * | 2015-02-20 | 2019-10-02 | 東洋紡株式会社 | マルチフィラメント |
US10626531B2 (en) | 2015-02-20 | 2020-04-21 | Toyobo Co., Ltd. | Multifilament and braid using same |
WO2020138971A1 (ko) * | 2018-12-28 | 2020-07-02 | 코오롱인더스트리 주식회사 | 폴리에틸렌 멀티필라멘트 교락사 및 그 제조방법 |
KR102146097B1 (ko) * | 2018-12-28 | 2020-08-19 | 코오롱인더스트리 주식회사 | 폴리에틸렌 멀티필라멘트 교락사 및 그 제조방법 |
JP7348394B2 (ja) * | 2019-12-27 | 2023-09-20 | コーロン インダストリーズ インク | 優れた寸法安定性を有するポリエチレン原糸およびその製造方法 |
JP7289931B2 (ja) * | 2019-12-27 | 2023-06-12 | コーロン インダストリーズ インク | ポリエチレン原糸、その製造方法、およびこれを含む冷感性生地 |
CN111607026A (zh) * | 2020-06-30 | 2020-09-01 | 上海化工研究院有限公司 | 一种易溶胀聚乙烯粉末及其制备方法和应用 |
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- 2001-08-08 JP JP2001241118A patent/JP4389142B2/ja not_active Expired - Fee Related
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2002
- 2002-08-02 US US10/486,110 patent/US7056579B2/en not_active Expired - Lifetime
- 2002-08-02 AT AT02753220T patent/ATE403766T1/de not_active IP Right Cessation
- 2002-08-02 WO PCT/JP2002/007910 patent/WO2003014437A1/ja active Application Filing
- 2002-08-02 CN CN02815479.7A patent/CN1271257C/zh not_active Expired - Fee Related
- 2002-08-02 DE DE60228115T patent/DE60228115D1/de not_active Expired - Lifetime
- 2002-08-02 EP EP02753220A patent/EP1445356B1/en not_active Expired - Lifetime
- 2002-08-02 KR KR1020097009396A patent/KR100951222B1/ko not_active IP Right Cessation
- 2002-08-02 KR KR1020047001868A patent/KR100909559B1/ko not_active IP Right Cessation
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WO1993008221A2 (en) * | 1991-10-15 | 1993-04-29 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
WO1993024686A1 (en) * | 1992-05-29 | 1993-12-09 | Borealis Holding A/S | Melt-spun high-strength polyethylene fibre |
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EP1493851A4 (en) * | 2002-04-09 | 2006-10-04 | Toyo Boseki | POLYETHYLENE FIBER AND THEIR PRODUCTION PROCESS |
US7247372B2 (en) | 2002-04-09 | 2007-07-24 | Toyo Boseki Kabushiki Kaisha | Polyethylene filament and a process for producing the same |
US7736564B2 (en) | 2002-04-09 | 2010-06-15 | Toyo Boseki Kabushiki Kaisha | Process of making a high strength polyolefin filament |
Also Published As
Publication number | Publication date |
---|---|
ATE403766T1 (de) | 2008-08-15 |
CN1271257C (zh) | 2006-08-23 |
JP2003049320A (ja) | 2003-02-21 |
DE60228115D1 (de) | 2008-09-18 |
US7056579B2 (en) | 2006-06-06 |
KR100951222B1 (ko) | 2010-04-05 |
EP1445356A4 (en) | 2005-08-31 |
KR20040023722A (ko) | 2004-03-18 |
KR100909559B1 (ko) | 2009-07-27 |
CN1539033A (zh) | 2004-10-20 |
US20050003182A1 (en) | 2005-01-06 |
EP1445356A1 (en) | 2004-08-11 |
JP4389142B2 (ja) | 2009-12-24 |
EP1445356B1 (en) | 2008-08-06 |
KR20090049099A (ko) | 2009-05-15 |
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