WO2021182429A1 - ポリアミド４６マルチフィラメント - Google Patents

ポリアミド４６マルチフィラメント Download PDF

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Publication number
WO2021182429A1
WO2021182429A1 PCT/JP2021/009132 JP2021009132W WO2021182429A1 WO 2021182429 A1 WO2021182429 A1 WO 2021182429A1 JP 2021009132 W JP2021009132 W JP 2021009132W WO 2021182429 A1 WO2021182429 A1 WO 2021182429A1
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WO
WIPO (PCT)
Prior art keywords
polyamide
multifilament
elongation
elongation rate
strength
Prior art date
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Ceased
Application number
PCT/JP2021/009132
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English (en)
French (fr)
Japanese (ja)
Inventor
上條太治
重野久雄
南井一志
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Toray Industries Inc
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Toray Industries Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP2021518977A priority Critical patent/JP7647550B2/ja
Priority to EP21768420.8A priority patent/EP4119705A4/en
Priority to US17/799,153 priority patent/US12584248B2/en
Priority to CN202180012603.1A priority patent/CN115053024B/zh
Publication of WO2021182429A1 publication Critical patent/WO2021182429A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
    • 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
    • D01D1/06—Feeding liquid to the spinning head
    • D01D1/09—Control of pressure, temperature or feeding rate
    • 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
    • D01D5/12—Stretch-spinning methods
    • 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
    • D01D5/12—Stretch-spinning methods
    • D01D5/16—Stretch-spinning methods using rollers, or like mechanical devices, e.g. snubbing pins
    • D—TEXTILES; PAPER
    • D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02J—FINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
    • D02J1/00—Modifying the structure or properties resulting from a particular structure; Modifying, retaining, or restoring the physical form or cross-sectional shape, e.g. by use of dies or squeeze rollers
    • D02J1/22—Stretching or tensioning, shrinking or relaxing, e.g. by use of overfeed and underfeed apparatus, or preventing stretch
    • D—TEXTILES; PAPER
    • D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02J—FINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
    • D02J1/00—Modifying the structure or properties resulting from a particular structure; Modifying, retaining, or restoring the physical form or cross-sectional shape, e.g. by use of dies or squeeze rollers
    • D02J1/22—Stretching or tensioning, shrinking or relaxing, e.g. by use of overfeed and underfeed apparatus, or preventing stretch
    • D02J1/228—Stretching in two or more steps, with or without intermediate steps
    • 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
    • D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/02—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides
    • 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
    • D10B2401/04—Heat-responsive characteristics

Definitions

  • the present invention relates to a polyamide 46 multifilament.
  • the multifilament manufactured using the aliphatic polyamide is a high-strength polyamide multifilament having excellent properties such as high strength and high elongation as compared with the multifilament made of other materials.
  • polyamide 66 is often used for belt cords because it has a high melting point and high strength among polyamides and is inexpensive.
  • the polyamide 46 has a higher melting point and higher heat resistance, and therefore has excellent thermal dimensional stability. Therefore, it is a material suitable for belt cords, and by improving spinning and drawing conditions.
  • a technique for improving strength (Patent Document 1) is disclosed.
  • a technique for enhancing thermal dimensional stability (Patent Documents 2 and 3) has also been disclosed, and there have been inventions for further enhancing the characteristics of the polyamide 46 as a belt cord.
  • Stretchability is a useful property not only for belt cords but also for sewing threads, for example, and if stretchability at high temperatures can be exhibited, the range of application in each application will be expanded.
  • a method for imparting stretchability to a polyamide multifilament for example, a method of using a semi-drawn yarn polyamide multifilament as a sheath yarn and performing Taslan processing with a core yarn polyamide multifilament is disclosed (Patent Document 4).
  • Patent Document 4 a method of using a semi-drawn yarn polyamide multifilament as a sheath yarn and performing Taslan processing with a core yarn polyamide multifilament.
  • the conventional technique does not provide a polyamide 46 multifilament having all of high strength, high thermal dimensional stability and excellent stretchability.
  • JP-A-59-88910 Japanese Unexamined Patent Publication No. 59-76914 Japanese Unexamined Patent Publication No. 1-168914 Japanese Unexamined Patent Publication No. 2002-249943
  • An object of the present invention is to solve the above problems, and to provide a polyamide 46 multifilament having high strength, high thermal dimensional stability and excellent stretchability.
  • the polyamide monofilament of the present invention has the following constitution.
  • the elongation rate (E'10) after heat treatment at a strength of 6.0 to 9.0 cN / dtex, an elongation of 15 to 30%, and 120 ° C. for 24 hours and then 10 times of tension in a room temperature environment is 2. Less than 5.5%, the difference (E'10) between the elongation rate (E'1) after one tensioning of the heat-treated fiber in a room temperature environment and the elongation rate (E'10) after ten times tensioning.
  • the polyamide 46 multifilament is characterized in that 10-E'1) is less than 0.60%.
  • the difference (E10-E1) between the elongation rate (E1) after one tension in a room temperature environment and the elongation rate (E10) after ten tensions in a room temperature environment is 0.70. It is preferable that it is less than%, the heat shrinkage rate at 120 ° C. is 0.5 to 2.0%, the relative viscosity of sulfuric acid is 3.0 to 5.0, and the total fineness is 300 dtex to 2300 dtex. ..
  • the polyamide 46 is melt-spun and the spun undrawn yarn is multi-stage drawn, and the multi-stage drawing consists of at least the first stage drawing and the final drawing. Is produced by stretching from 1.00 to 1.10. Furthermore, the polyamide 46 multifilament is produced by melting under vacuum during melt spinning.
  • the polyamide 46 multifilament of the present invention will be described below.
  • the polyamide 46 multifilament of the present invention is made of a polyamide resin.
  • a polyamide resin whose main component is polyamide 46 is preferable.
  • polyamide resin in which 98% by mass or more is composed of the polyamide 46, and more preferably it is composed of only the polyamide 46, out of the total mass excluding the additives described later.
  • Polyamide 46 and other polyamides can be copolymerized and used, and polyamide 6, polyamide 66, polyamide 610, and polyamide 612 can be used as the polyamide used for the copolymerization. Further, it may be a mixture of the polyamide 46 and another polyamide.
  • the polyamide resin contains 250 to 7,000 ppm, preferably 500 to 7,000 ppm of conventionally known heat-resistant agents such as copper compounds such as inorganic and organic copper salts and simple copper metals, amine compounds, mercapto compounds, phosphorus compounds, and hindered phenol compounds. It is preferable to add 5000 ppm. These may be used alone or in combination of two or more. If the amount of these heat resistant agents is less than 250 ppm, the suppression of thermal deterioration of the polymer is limited, and the strength and elongation of the filament decreases at high temperatures. On the other hand, if a heat resistant agent exceeding 7,000 ppm is added, the strength and elongation of the fiber tends to be impaired.
  • conventionally known heat-resistant agents such as copper compounds such as inorganic and organic copper salts and simple copper metals, amine compounds, mercapto compounds, phosphorus compounds, and hindered phenol compounds. It is preferable to add 5000 ppm. These may be used alone or in
  • the relative sulfuric acid viscosity of the polyamide 46 which is the raw material of the polyamide 46 multifilament of the present invention, is preferably 3.0 to 5.0, more preferably 3.5 to 5.0. If the relative viscosity of sulfuric acid exceeds the above range, it contributes to the deterioration of the spinnability and tends to cause frequent yarn breakage and fluffing during drawing. Further, if the relative viscosity of sulfuric acid is less than 3.5, the molecular chain of the polyamide is short, so that the stretchability and thermal dimensional stability required for the above application cannot be exhibited. Sulfuric acid relative viscosity refers to the value measured by the method described in the column of Examples.
  • the polyamide 46 multifilament of the present invention preferably has a fineness of 300 to 2300 dtex, more preferably 400 to 1700 dtex. If the fineness is less than 200 dtex, the fineness is too fine, and there is a high possibility that fluff will be generated during thermal drawing of the multifilament after melt spinning. When the fineness exceeds 2300 dtex, for example, it becomes difficult to use it as a sewing thread, and the uniform cooling property at the time of spinning deteriorates, so that the quality of the raw thread deteriorates, and the strength and durability of the belt deteriorate. It may end up.
  • the number of single fibers of the polyamide 46 multifilament of the present invention is preferably 30 to 350, and more preferably 50 to 250. If the number of fibers is less than this range, the fineness of the single fiber becomes thicker, the cooling efficiency at the time of melt spinning becomes low, and the flexibility of the multifilament tends to be lost. Further, when the number of fibers is larger than the number range, the fineness of the single fiber becomes thin, and fluff tends to be easily generated.
  • the strength of the polyamide 46 multifilament of the present invention is indispensable to be 6.0 to 9.0 cN / dtex, more preferably 7.0 to 9.0 cN / dtex.
  • This strength range is also a characteristic required for polyamide multifilaments when used in many products, and it has been clarified that it is an essential range for obtaining polyamide 46 multifilaments that have both thermal dimensional stability and stretchability. Is.
  • the strength refers to a value measured by the method described in the column of Examples.
  • the elongation (breaking elongation) of the polyamide 46 multifilament of the present invention is essential to be 15 to 30%, more preferably 18 to 30%. Within such a range, when a load is applied to the belt, the impact can be absorbed by expansion and contraction, and the durability of the belt can be maintained.
  • the elongation refers to the value measured by the method described in the column of Examples.
  • the cross-sectional shape of the single fiber of the polyamide 46 multifilament of the present invention is not particularly limited. It is possible to adopt a cross section having various shapes such as a round cross section, a flat cross section, a polygonal cross section, a deformed shape such as a Y type or an X type, and a hollow cross section. It may be a mixed fiber having a plurality of cross-sectional shapes.
  • the polyamide 46 multifilament of the present invention has a difference between the elongation rate (E1) after being pulled once in a room temperature environment and the elongation rate (E10) after being pulled 10 times in a room temperature environment (E10).
  • E10-E1) is preferably less than 0.70%. More preferably, it is less than 0.60%. If this range is exceeded, hysteresis loss will increase when used as a belt cord, and the tension of the belt will decrease as the usage time increases, making the product unsuitable for medium- to long-term use. ..
  • the repeated tensile test and the calculation method of the elongation rate will be described in the column of Examples.
  • the elongation rate (E'10) after 10 times tensioning of the fiber after treatment at 120 ° C. for 24 hours in a room temperature environment is less than 2.5%, more preferably 2.0. Less than%. Further, the difference (E'10-) between the elongation rate (E'1) after the heat-treated fiber is pulled once in a room temperature environment and the elongation rate (E'10) after being pulled 10 times. It is essential that E'1) is less than 0.60%, more preferably less than 0.50%. When using the belt, the temperature of the belt and the cord becomes high depending on the load, friction, and usage environment.
  • the heat shrinkage rate of the polyamide 46 multifilament of the present invention at 120 ° C. is preferably 0.5 to 2.0%, more preferably 0.5 to 1.7%. If it is lower than this heat shrinkage rate, tension is not generated due to the temperature rise due to friction during belt driving, so that the multifilament may lose its stretchability. Further, if the heat shrinkage range is exceeded, the thermal dimensional stability may be impaired.
  • the polyamide 46 multifilament of the present invention is preferably produced by melt spinning, and as described above, the nylon 46 resin used for melt spinning preferably has a sulfuric acid relative viscosity of 3.0 to 5.0, more preferably 3.5 to 5.0. It is 5.0. Within such a range, a high-strength nylon 46 multifilament can be stably obtained in a state where the spinnability is good.
  • FIG. 1 shows an outline of one aspect of the method for producing the polyamide 46 multifilament of the present invention (the melting step is not shown).
  • polyamide 46 resin is melted and kneaded by an extruder type spinning machine and spun, but it is preferable that the melting is performed in a vacuum environment. Under a vacuum environment, the pressure at the resin supply port of the extruder is preferably less than 5 kPa, more preferably less than 3 kPa.
  • Polyamide 46 has a property of thickening at the time of melting and decomposing at the time of melting to produce a low molecular weight body, unlike other aliphatic polyamides that produce a high molecular weight body.
  • the decomposition mechanism can be roughly divided into thermal decomposition, oxidative decomposition, and hydrolysis.
  • the spinning temperature is set to 10 to 50 ° C. higher than the melting point of the polymer, and melt spinning is performed from a mouthpiece 1 having a plurality of holes, preferably 30 to 350, more preferably 50 to 250, and 5 from directly below the spinning mouthpiece. It is preferable to surround a range of about 300 cm with a heating cylinder 2 and allow the melt-spun yarn to pass through a high temperature atmosphere of ⁇ 30 to + 30 ° C. with respect to the melting point.
  • the high temperature atmosphere to be passed is more preferably a melting point of ⁇ 15 to + 15 ° C.
  • the undrawn yarn that has passed the above steps is cooled and solidified by blowing air at 10 to 80 ° C., preferably 10 to 50 ° C. by the cross-flow cooling device 3. If the cooling air is less than 10 ° C., a large cooling device is required, which is not preferable. Further, when the cooling air exceeds 80 ° C., an air volume is required and the single fiber sway becomes large, so that the single fibers collide with each other and cause deterioration of the silk reeling property.
  • the undrawn yarn that has been cooled and solidified is then drawn in multiple stages, particularly in two or three stages.
  • an oil agent is applied to the cooled and solidified undrawn yarn by the oil supply device 4, and the undrawn yarn is picked up by the take-up roller (1FR) 6.
  • the take-up roller is usually unheated.
  • the yarn is wound in the order of the yarn feeding roller (2FR) 7, the first stretching roller (1DR) 8, the second stretching roller (2DR) 9, the third stretching roller (3DR) 10, and the relaxation roller (RR) 11. It is rotated to perform heat treatment and stretching treatment, and is wound around a winder 12.
  • the surface of 2FR is preferably a mirror surface, and the surface of 1DR, 2DR, 3DR, and RR is preferably satin finished.
  • the first step is stretched between 2FR and 1DR, and the temperature of 2FR (surface temperature of the roller) is 30 to 50 ° C, and the temperature of 1DR is 100 to 225 ° C.
  • the second stage stretching is performed between 1DR and 2DR, and the temperature of 2DR (the surface temperature of the roller) is 150 to 230 ° C.
  • the third stage stretching is performed between 2DR and 3DR, and the temperature of 3DR (the surface temperature of the roller) is 180 to 240 ° C.
  • the draw ratio of the third-stage stretching step that is, the final stretching step is 1.00 to 1.10, and the stretching ratio is 1. It is more preferably 00 to 1.05.
  • the draw ratio is larger than the above range, the orientation of the amorphous portion of the molecular chain becomes high, so that the thermal dimensional stability deteriorates, and when the generation of fluff becomes remarkable, the strength tends to be impaired. If the draw ratio is lower than 1.00 times, the tension is lowered, so that the yarn swings greatly and the yarn production may be difficult.
  • a fiber with a test length of 250 mm is sandwiched between the chucks of A &D's Tencilon tensile tester RTG-1250 under a 25 ° C environment, and A &D's high-temperature environment tank TLF-3R / F / G- Set S and perform treatment at 120 ° C. for 24 hours.
  • Example 1 Manufacturing method of polyamide 46 multifilament
  • the manufacturing process shown in FIG. 1 was used.
  • a polyamide 46 resin (“Stanyl” (registered trademark), melting point 292 ° C.) having a relative sulfuric acid viscosity of 3.9 was melted at 305 ° C. under vacuum using an extruder type spinning machine.
  • the molten polymer was weighed with a gear pump so that the total fineness was 940 dtex, filtered through a 20 ⁇ metal non-woven fabric filter in a spinning pack, and spun from a 136-hole round hole base.
  • a heating cylinder having a heating cylinder length of 15 cm was installed 3 cm below the surface of the mouthpiece, and heated so that the temperature inside the cylinder was 300 ° C. so that the spun yarn passed under the atmosphere of 300 ° C.
  • the in-cylinder atmospheric temperature is the air temperature at the central portion of the length of the heating cylinder, which is 1 cm away from the inner wall.
  • a uniflow type chimney that blows air from one direction is attached directly under the heating cylinder, and after passing through the heating cylinder, cold air at 20 ° C is blown at a speed of 35 m / min to cool and solidify, and then the yarn is made into a yarn by a refueling device.
  • An oil agent was applied.
  • the undrawn yarn to which the oil agent was applied was wound around 1FR rotating at a surface speed of 600 m / min and taken up, and then drawn at a total draw ratio of 4.70 times.
  • the take-up thread is continuously stretched by 5% between the take-up roller and 2FR without being wound once, and then the first step is stretched at a rotation speed ratio of 3.27 times, and then the rotation speed.
  • the second-stage stretching was performed at a ratio of 1.30 times, and finally the final stretching of the third stage was performed at a rotation speed ratio of 1.05 times, and the film was wound at a speed of 2600 m / min.
  • the roller surface of 1FR and 2FR is mirror-finished, 1DR, 2DR, 3DR and RR are satin-finished, and the roller temperature is 1FR unheated, 2FR 80 ° C., 1DR 175 ° C., and 2DR 180 ° C.
  • the 3DR was 230 ° C. and the RR was 150 ° C.
  • Nylon 46 multifilament was obtained by such melt spinning and stretching (Table 1).
  • Example 2 The same procedure as in Example 1 was carried out except that the third-stage draw ratio (final draw ratio) was set to 1.00 when the nylon 46 multifilament was spun.
  • Example 3 During melt spinning, the molten polymer was weighed with a gear pump so that the fineness was 1400 dtex, and the same procedure as in Example 1 was carried out except that a 204-hole round hole was used for the mouthpiece.
  • Example 4 Example 1 except that the molten polymer was weighed with a gear pump so that the fineness was 470 dtex at the time of melt spinning, a 72-hole round hole was used for the mouthpiece, and the drawing was performed at a total draw ratio of 4.20 times. I went in the same way.
  • Example 5 The same as in Example 1 was carried out except that the two-stage stretching was performed and the final stretching ratio was 1.08 times.
  • Example 1 The same procedure as in Example 1 was carried out except that the final draw ratio was 1.25 times.
  • Example 2 The same procedure as in Example 1 was carried out except that the final draw ratio was 0.90 times.
  • Example 3 The same as in Example 1 was carried out except that melt spinning with an extruder type spinning machine was carried out under normal pressure.
  • Example 4 The same procedure as in Example 4 was carried out except that the molten polymer was weighed with a gear pump so that the fineness was 235 dtex during melt spinning.
  • Table 1 shows the production conditions in Examples 1 to 5 and Comparative Examples 1 to 6, and Table 2 shows the results of evaluating the physical properties of the obtained polyamide 46 multifilament.
  • the polyamide 46 multifilament of the present invention has high strength, high thermal dimensional stability, and exhibits excellent stretchability.
  • Comparative Example 3 the polymer is decomposed by melting under normal pressure, a high-strength multifilament cannot be obtained, and the crystallinity is low, so that the stretchability is disadvantageous. ..
  • Comparative Example 1 when the high-strength polyamide 46 multifilament is produced, if the draw ratio in the final drawing step exceeds 1.1, crystallization does not occur and thermal dimensional stability or stretch is not exhibited. The sex gets worse. On the other hand, in Comparative Example 2, since the draw ratio in the final drawing step was less than 1.0, yarn breakage occurred frequently and it was difficult to collect the raw yarn.
  • the polyamide 46 multifilament of the present invention not only has high durability due to its high strength, but also has high heat resistance, high thermal dimensional stability, and excellent stretchability. Therefore, when used as a belt cord, the polyamide 46 multifilament has high strength.
  • the belt does not require an auto tensioner, and the cost of the belt drive unit as a whole can be reduced. Further, taking advantage of the high strength and high stretchability of the polyamide 46 multifilament, it can be used as a sewing thread for clothing such as sports applications.

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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)
  • Artificial Filaments (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
PCT/JP2021/009132 2020-03-13 2021-03-09 ポリアミド４６マルチフィラメント Ceased WO2021182429A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2021518977A JP7647550B2 (ja) 2020-03-13 2021-03-09 ポリアミド４６マルチフィラメント
EP21768420.8A EP4119705A4 (en) 2020-03-13 2021-03-09 POLYAMIDE MULTIFILAMENT
US17/799,153 US12584248B2 (en) 2020-03-13 2021-03-09 Polyamide 46 multifilament
CN202180012603.1A CN115053024B (zh) 2020-03-13 2021-03-09 聚酰胺46复丝

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JP2020043988 2020-03-13
JP2020-043988 2020-03-13

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WO2021182429A1 true WO2021182429A1 (ja) 2021-09-16

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US (1) US12584248B2 (https=)
EP (1) EP4119705A4 (https=)
JP (1) JP7647550B2 (https=)
CN (1) CN115053024B (https=)
TW (1) TW202140874A (https=)
WO (1) WO2021182429A1 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023038098A1 (ja) * 2021-09-10 2023-03-16 東レ株式会社 ポリアミド４６マルチフィラメントおよびエアバッグ縫製糸

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS507169B1 (https=) * 1970-12-28 1975-03-22
JPS5976914A (ja) 1982-10-22 1984-05-02 Toray Ind Inc ポリアミド繊維およびその製造方法
JPS5988910A (ja) 1982-11-04 1984-05-23 Unitika Ltd 高強力ナイロン４６繊維及びその製造
JPS5988942A (ja) * 1982-11-08 1984-05-23 東レ株式会社 ポリアミドタイヤコ−ド及びその製法
JPH02210018A (ja) * 1989-02-01 1990-08-21 Unitika Ltd Ｖベルト補強用ポリアミド繊維
JPH1168914A (ja) 1997-08-18 1999-03-09 Ricoh Co Ltd ファクシミリ装置
JP2002249943A (ja) 2001-02-27 2002-09-06 Kanebo Ltd ナイロンストレッチ糸とそれを使用したスパンライク織物
JP2009243030A (ja) * 2008-03-10 2009-10-22 Toray Ind Inc エアバッグ用基布ならびにエアバッグ用原糸およびその製造方法
JP2014037642A (ja) * 2012-08-14 2014-02-27 Mitsubishi Gas Chemical Co Inc ポリエーテルポリアミド繊維

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5247596B2 (https=) 1973-05-23 1977-12-03
JPH01168914A (ja) 1987-12-21 1989-07-04 Toray Ind Inc ポリテトラメチレンアジパミド系繊維
DE3817941A1 (de) * 1988-05-27 1989-11-30 Rhodia Ag Extrusionsverfahren und ein-, zwei- oder mehrschneckenextruder
CA2450103C (en) * 2003-10-22 2008-09-16 Hyosung Corporation Low shrinkage polyamide fiber and uncoated fabric for airbags made of the same
EP2886687A4 (en) 2012-08-14 2016-03-30 Mitsubishi Gas Chemical Co POLYETHERPOLYAMIDFASER

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS507169B1 (https=) * 1970-12-28 1975-03-22
JPS5976914A (ja) 1982-10-22 1984-05-02 Toray Ind Inc ポリアミド繊維およびその製造方法
JPS5988910A (ja) 1982-11-04 1984-05-23 Unitika Ltd 高強力ナイロン４６繊維及びその製造
JPS5988942A (ja) * 1982-11-08 1984-05-23 東レ株式会社 ポリアミドタイヤコ−ド及びその製法
JPH02210018A (ja) * 1989-02-01 1990-08-21 Unitika Ltd Ｖベルト補強用ポリアミド繊維
JPH1168914A (ja) 1997-08-18 1999-03-09 Ricoh Co Ltd ファクシミリ装置
JP2002249943A (ja) 2001-02-27 2002-09-06 Kanebo Ltd ナイロンストレッチ糸とそれを使用したスパンライク織物
JP2009243030A (ja) * 2008-03-10 2009-10-22 Toray Ind Inc エアバッグ用基布ならびにエアバッグ用原糸およびその製造方法
JP2010100988A (ja) * 2008-03-10 2010-05-06 Toray Ind Inc エアバッグ用基布ならびにエアバッグ用原糸およびその製造方法
JP2014037642A (ja) * 2012-08-14 2014-02-27 Mitsubishi Gas Chemical Co Inc ポリエーテルポリアミド繊維

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP4119705A4

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023038098A1 (ja) * 2021-09-10 2023-03-16 東レ株式会社 ポリアミド４６マルチフィラメントおよびエアバッグ縫製糸

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