EP3760774A1 - Preparation method for long continuous electrospun polyacrylonitrile nanofiber yarn, and application thereof - Google Patents

Preparation method for long continuous electrospun polyacrylonitrile nanofiber yarn, and application thereof Download PDF

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Publication number
EP3760774A1
EP3760774A1 EP19909629.8A EP19909629A EP3760774A1 EP 3760774 A1 EP3760774 A1 EP 3760774A1 EP 19909629 A EP19909629 A EP 19909629A EP 3760774 A1 EP3760774 A1 EP 3760774A1
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EP
European Patent Office
Prior art keywords
filament yarn
continuous filament
polyacrylonitrile
electrospun
preparing
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.)
Pending
Application number
EP19909629.8A
Other languages
German (de)
French (fr)
Other versions
EP3760774A4 (en
Inventor
Haoqing Hou
Wen OUYANG
Yuming Wang
Chuyun Cheng
Qi Wang
Xiaoyi Lv
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jiangxi Advanced Nanofiber S&t Co Ltd
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Jiangxi Advanced Nanofiber S&t Co Ltd
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Application filed by Jiangxi Advanced Nanofiber S&t Co Ltd filed Critical Jiangxi Advanced Nanofiber S&t Co Ltd
Publication of EP3760774A1 publication Critical patent/EP3760774A1/en
Publication of EP3760774A4 publication Critical patent/EP3760774A4/en
Pending legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/0007Electro-spinning
    • D01D5/0015Electro-spinning characterised by the initial state of the material
    • D01D5/003Electro-spinning characterised by the initial state of the material the material being a polymer solution or dispersion
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/42Formation of filaments, threads, or the like by cutting films into narrow ribbons or filaments or by fibrillation of films or filaments
    • D01D5/426Formation of filaments, threads, or the like by cutting films into narrow ribbons or filaments or by fibrillation of films or filaments by cutting films
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/18Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/02Yarns or threads characterised by the material or by the materials from which they are made
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/02Yarns or threads characterised by the material or by the materials from which they are made
    • D02G3/06Threads formed from strip material other than paper
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/22Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
    • D02G3/26Yarns or threads characterised by constructional features, e.g. blending, filament/fibre with characteristics dependent on the amount or direction of twist
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02JFINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
    • D02J1/00Modifying 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
    • D02J1/22Stretching or tensioning, shrinking or relaxing, e.g. by use of overfeed and underfeed apparatus, or preventing stretch
    • D02J1/223Stretching in a liquid bath
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02JFINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
    • D02J1/00Modifying 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
    • D02J1/22Stretching or tensioning, shrinking or relaxing, e.g. by use of overfeed and underfeed apparatus, or preventing stretch
    • D02J1/228Stretching in two or more steps, with or without intermediate steps
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING 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
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/005Synthetic yarns or filaments
    • D04H3/007Addition polymers
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING 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
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/02Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of yarns or filaments
    • D04H3/03Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of yarns or filaments at random
    • D04H3/033Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of forming fleeces or layers, e.g. reorientation of yarns or filaments at random reorientation immediately after yarn or filament formation
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2321/00Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D10B2321/10Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide

Definitions

  • the present invention relates to the field of continuous filament yarn of polymer fibers, in particular to a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers and uses thereof.
  • Polyacrylonitrile fiber commonly known as acrylic fiber or artificial wool
  • acrylic fiber or artificial wool is a commonly used artificial fiber that can be used to replace or blended with wool to make wool fabrics. It has a good effect of warmth retention, and it also has excellent weather resistance and light resistance, after one year of open-air exposure, the intensity only decreases by 20%, so it is often used to make curtains, tarpaulins, etc.
  • Eelectrostatic spinning is a special fiber manufacturing process, and has been used more and more in the past ten years to prepare nanofiber materials. Its working method is as follows: the polymer solution or the melt is jetted out in a high-voltage electric field, solidified in a running distance, and finally the spinning is received by a receiving device. Due to the process of electrostatic spinning is simple, and various forms of fibers can also be produced according to demand, such as solid fibers, hollow fibers, core-shell structure fibers, etc., it has broad prospects in many fields.
  • the current electrostatic spinning technology is only used to manufacture a non-woven fabric or spray a thin layer of nano-cobweb on industrial non-woven fabrics (generally with an areal density of about 1 g/m 2 ), which can also manufacture discontinuous and higher linear density of thick yarn, and there is no technology in the world that can continuously manufacture ultra-small linear density or ultra-high count yarn of electrospun nanofibers.
  • the linear density of conventional fiber yarns is above 6 Tex, and the counts of the yarns are generally less than 150 counts, and most of them are below 100 counts.
  • the first aspect of the present invention provides a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • the polar solvent in the step a is one or more selected from the group consisting of N, N-dimethylformamide, N-methylpyrrolidone, dimethyl sulfoxide, and N, N-dimethylacetamide.
  • the water bath draft and air draft in the step d are 5-roll drafts.
  • the unwinding speed of the water bath draft in the step d is 2 to 8 m/min.
  • the unwinding speed of the air draft in the step d is 3 to 8 m/min.
  • the fiber orientation degree of the fiber bundle in the step d is 90% to 95%.
  • the unwinding speed of twisting in the step e is 5 to 50 m/min.
  • the twist degree of twisting in the step e is 500 to 1500 twist/m.
  • the second aspect of the present invention provides a continuous filament yarn of electrospun polyacrylonitrile nanofibers, which is prepared by the above method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
  • the third aspect of the present invention provides a use of the continuous filament yarn of electrospun polyacrylonitrile nanofibers, that is, for pure or blended spinning to weave a light-weight and warm high-grade fabric.
  • the present invention provides a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, which enhance the mechanical properties of polyacrylonitrile fibers through draft operation and can produce continuously, and the produced filament yarns have a length of not less than 2000 meters and a metric count of more than 500, which can be used for pure or blended spinning to obtain a light-weight, warm and durable high-grade fabric.
  • the present invention provides a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • step a The objective of step a is to prepare a polymer solution suitable for electrostatic spinning, and because there are a large number of polar cyano groups in polyacrylonitrile, selecting a suitable polar solvent helps to prepare a spinning solution with suitable concentration and adjustable viscosity.
  • Step a dissolving a polyacrylonitrile raw material in a polar solvent under mechanical stirring to obtain a uniform spinning solution.
  • the polyacrylonitrile raw material and the polar solvent are added together in a stainless steel reactor and dissolved under mechanical stirring to obtain a uniform polyacrylonitrile solution for spinning.
  • the polyacrylonitrile raw material in the present invention is not particularly limited, and may be commercially available, and the CAS number is 25014-41-9.
  • the polar solvent in step a is selected from one or more of N, N-dimethylformamide ( CAS number: 68-12-2 ), N-methylpyrrolidone ( CAS number: 872-50-4 ), dimethyl sulfoxide ( CAS No. 67-68-5 ) and N, N-dimethylacetamide ( CAS No. 127-19-5 ).
  • Both dimethyl sulfoxide and N-methylpyrrolidone are good solvents for dissolving polyacrylonitrile, and dimethyl sulfoxide is non-toxic, but both have boiling points above 200°C, and the spun yarns are not easy to dry and have serious adhesion to each other.
  • N, N-dimethylformamide has the lowest boiling point among several listed solvents and has the best solubility, while N, N-dimethylacetamide has relatively low solubility, but has the advantage of low toxicity which can be compounded with N, N-dimethylformamide to make a mixed solvent for spinning.
  • the polar solvent in the step a is N, N-dimethylformamide and/or N, N-dimethylacetamide; further preferably, the N, N-Dimethylformamide and N, N-dimethylacetamide; further, the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide is 4: 1.
  • the concentration of the spinning solution determines the viscosity of the solution, if the viscosity is too large, the electrostatic force needs to overcome a greater surface tension, making the spinning diameter too large or even impossible to spin; and too small viscosity will make the spinning too thin, insufficient strength, or beads may appear on the spinning.
  • the mass concentration of the solution in the step a is 12 to 22%; further preferably, the mass concentration of the solution in the step a is 13 to 18%.
  • the absolute viscosity of the solution in the step a is 1.5 to 5 Pa.S; further preferably, the absolute viscosity of the solution in the step a is 2 to 4 Pa.S.
  • dissolution temperature in the step a is 30 to 55°C. and the stirring time is 4 to 10 hours; further preferably, the dissolution temperature in the step a is 38 to 48°C. and the stirring time is 6 to 9 hours.
  • the objective of the step b is to make polyacrylonitrile from solution into a nonwoven fabric, in this process, the polymer solution is sprayed into a strong electric field. Under the action of the electric field, the sprayed droplets change from spherical to Taylor cone, from the tip of which a tiny jet is extended, and after running for a certain distance, the jet is solidified into fiber filaments, which are collected by a stainless steel mesh belt to obtain a nonwoven fabric.
  • Step b making the polyacrylonitrile solution in the step a into a polyacrylonitrile nonwoven fabric in an electrospinning machine.
  • the polyacrylonitrile solution is injected into the spinning device of an electrospinning machine, spraying spun in a high-voltage electric field, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric.
  • the DC voltage of the high-voltage electric field in the step b is 30 to 50 kV; further preferably, the DC voltage of the high-voltage electric field in the step b is 40 to 45 kV.
  • the distance between the spinneret and the stainless steel mesh belt collector requires to ensure that the jet can be solidified during running without adhesion, and improper receiving distance will cause beads appeared in the spinning fibers.
  • the distance between the spinneret and the stainless steel mesh belt collector in the step b is 25 to 55 cm; further preferably, the distance between the spinneret and the stainless steel mesh belt collector is 28 to 35 cm.
  • the travel speed of the stainless steel mesh belt can affect the pore size and thickness of the nonwoven fabric, which in turn affects the strength of the filament yarn processed from the nonwoven fabric.
  • the travel speed of the stainless steel mesh belt in the step b is 1 to 5 m/min; further preferably, the travel speed of the stainless steel mesh belt is 2 to 4 m/min.
  • the diameter of the spinning in step b is 100-1500 nm; further preferably, the diameter of the spinning in the step b is 100 to 500 nm.
  • the objective of the step c is to pretreat the polyacrylonitrile nonwoven fabric into a form suitable for further processing.
  • Step c cutting the nonwoven fabric in the step b into slender strips with a width of 0.5 to 6 cm.
  • the width of the cut strip will affect the subsequent further processing, and too narrow cut strip is not conducive to continuous production, making the resulting yarn easily broken, and it is impossible to achieve the ideal length to obtain a filament yarn; while too wide cut strip is difficult to process to obtain a fiber bundle with highly oriented internal fibers.
  • the width of the slender strip in the step c is 0.5 to 6 cm; further preferably, the width of the slender strip is 2 to 5.5 cm.
  • the objective of the step d is, on the one hand, to obtain a fiber bundle length sufficient to produce continuous filament yarns through drafting, and on the other hand, to change the degree of orientation of the internal fibers, making the strength of the fiber bundle in the orientation direction increased greatly .
  • Step d drafting the slender strips in the step c in a water bath at 80 to 95°C with a draft ratio of 2 to 5 times, then drafting in air at 110 to 150°C with a draft ratio of 3 to 10 times to obtain a fiber bundle with highly oriented internal fibers.
  • the water bath draft and air draft in the step d are 5-roll drafts.
  • the unwinding speed of the water bath draft is 2 to 8 m/min; further preferably, the unwinding speed of the water bath draft is 4 to 7 m/min.
  • the unwinding speed of the air draft is 3 to 8 m/min; further preferably, the unwinding speed of the air draft is 4 to 7 m/min.
  • the fiber orientation degree of the fiber bundle in the step d is 90% to 95%.
  • the objective of the step e is to twist the fiber bundle into a filament yarn. After twisting, the outer fiber and the inner fiber squeeze each other to generate pressure, making the yarn obtain frictional force along the fiber length, and the fiber strip is longitudinally fixed, and the fiber after yarn formation has improved properties such as strength, elongation, gloss, and feel.
  • Step e twisting the fiber bundle in the step d to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers with a length of not less than 2000 meters.
  • the unwinding speed of twisting in the step e is 5 to 50 m/min; further preferably, the unwinding speed of twisting is 20 to 40 m/min.
  • the twist degree of twisting in the step e is 500 to 1500 twist/m; further preferably, the twist degree of twisting in the step e is 800 to 1200 twist/m.
  • the strength of polyacrylonitrile nanofibers is lower.
  • the strength of polyacrylonitrile fiber after high drafting is further improved, which broadens its range of application.
  • filament yarn can be produced continuously, which in turn can be used for pure or blended with other fibers to weave alight-weight, warm, soft, and comfortable high-grade fabric.
  • Example 1 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 2 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 3 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 4 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 5 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 6 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 7 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 8 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 9 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • Example 10 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
  • the continuous filament yarns of electrospun polyacrylonitrile nanofibers obtained in examples 1 to 10 were tested for metric count, tensile strength, Young's modulus, and elongation at break.
  • Example 1 Metric count Tensile strength Young's modulus Elongation at break Example 1 740 15 cN/dtex 298 cN/dtex 11% Example 2 720 14.5 cN/dtex 290 cN/dtex 12% Example 3 660 12 cN/dtex 246 cN/dtex 19% Example 4 760 3 cN/dtex 84 cN/dtex 12% Example 5 700 13 cN/dtex 260 cN/dtex 14% Example 6 450 6 cN/dtex 108 cN/dtex 32% Example 7 520 11.5 cN/dtex 223 cN/dtex 27% Example 8 800 8 cN/dtex 130 cN/dtex 10% Example 9 630 10 cN/dtex 194 cN/dtex 22% Example 10 600 9.5 cN/dtex 172

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Nonwoven Fabrics (AREA)
  • Artificial Filaments (AREA)

Abstract

A method a for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps: a. dissolving a polyacrylonitrile raw material in a polar solvent under mechanical stirring to obtain a uniform spinning solution; b. mading the polyacrylonitrile solution in the step a into a polyacrylonitrile nonwoven fabric in an electrospinning machine; c. cutting the nonwoven fabric in the step b into slender strips with a width of 0.5 to 6 cm; d. drafting the slender strips in the step c in a water bath at 80-95°C with a draft ratio of 2 to 5 times, then drafting in air at 110 to 150°C with a draft ratio of 3 to 10 times to obtain a fiber bundle with highly oriented internal fibers; e. twisting the fiber bundle in the step d to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers with a length of not less than 2000 meters.

Description

    Technical Field
  • The present invention relates to the field of continuous filament yarn of polymer fibers, in particular to a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers and uses thereof.
  • Background
  • Polyacrylonitrile fiber, commonly known as acrylic fiber or artificial wool, is a commonly used artificial fiber that can be used to replace or blended with wool to make wool fabrics. It has a good effect of warmth retention, and it also has excellent weather resistance and light resistance, after one year of open-air exposure, the intensity only decreases by 20%, so it is often used to make curtains, tarpaulins, etc.
  • Eelectrostatic spinning is a special fiber manufacturing process, and has been used more and more in the past ten years to prepare nanofiber materials. Its working method is as follows: the polymer solution or the melt is jetted out in a high-voltage electric field, solidified in a running distance, and finally the spinning is received by a receiving device. Due to the process of electrostatic spinning is simple, and various forms of fibers can also be produced according to demand, such as solid fibers, hollow fibers, core-shell structure fibers, etc., it has broad prospects in many fields.
  • However, the current electrostatic spinning technology is only used to manufacture a non-woven fabric or spray a thin layer of nano-cobweb on industrial non-woven fabrics (generally with an areal density of about 1 g/m2), which can also manufacture discontinuous and higher linear density of thick yarn, and there is no technology in the world that can continuously manufacture ultra-small linear density or ultra-high count yarn of electrospun nanofibers. The linear density of conventional fiber yarns is above 6 Tex, and the counts of the yarns are generally less than 150 counts, and most of them are below 100 counts.
  • Summary
  • To solve the above technical problems, the first aspect of the present invention provides a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    1. a. dissolving a polyacrylonitrile raw material in a polar solvent under mechanical stirring to obtain a uniform spinning solution;
    2. b. making the polyacrylonitrile solution in the step a into a polyacrylonitrile nonwoven fabric in an electrospinning machine;
    3. c. cutting the nonwoven fabric in the step b into slender strips with a width of 0.5 to 6 cm;
    4. d. drafting the slender strips in the step c in a water bath at 80 to 95°C with a draft ratio of 2 to 5 times, then drafting in air at 110 to 150°C with a draft ratio of 3 to 10 times to obtain a fiber bundle with highly oriented internal fibers;
    5. e. twisting the fiber bundle in the step d to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers with a length of not less than 2000 meters.
  • Accoding to a preferred embodiment, the polar solvent in the step a is one or more selected from the group consisting of N, N-dimethylformamide, N-methylpyrrolidone, dimethyl sulfoxide, and N, N-dimethylacetamide.
  • Accoding to another preferred embodiment, the water bath draft and air draft in the step d are 5-roll drafts.
  • Accoding to another yet preferred embodiment, the unwinding speed of the water bath draft in the step d is 2 to 8 m/min.
  • Accoding to another yet preferred embodiment, the unwinding speed of the air draft in the step d is 3 to 8 m/min.
  • Accoding to another yet preferred embodiment, the fiber orientation degree of the fiber bundle in the step d is 90% to 95%.
  • Accoding to another yet preferred embodiment, the unwinding speed of twisting in the step e is 5 to 50 m/min.
  • Accoding to another yet preferred embodiment, the twist degree of twisting in the step e is 500 to 1500 twist/m.
  • The second aspect of the present invention provides a continuous filament yarn of electrospun polyacrylonitrile nanofibers, which is prepared by the above method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
  • The third aspect of the present invention provides a use of the continuous filament yarn of electrospun polyacrylonitrile nanofibers, that is, for pure or blended spinning to weave a light-weight and warm high-grade fabric.
  • Beneficial effects: the present invention provides a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, which enhance the mechanical properties of polyacrylonitrile fibers through draft operation and can produce continuously, and the produced filament yarns have a length of not less than 2000 meters and a metric count of more than 500, which can be used for pure or blended spinning to obtain a light-weight, warm and durable high-grade fabric.
  • Detailed Description of The Embodiments
  • The content of the present invention can be further understood in conjunction with the following detailed description of the preferred implementation methods of the present invention and the included embodiments. Unless otherwise stated, all the technical and scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art to which the application belongs. If the definition of a specific term disclosed in the prior art is inconsistent with any definition provided in this application, the definition of the term provided in this application shall prevail.
  • As used herein, unless the context clearly indicates otherwise, features that do not define singular and plural forms are also intended to include features of the plural form. It should also be understood that, as used herein, the term "prepared from" is synonymous with "comprise", "include", "including", "having", " comprise" and/or "comprising", when used in this specification, they mean the stated composition, step, method, article or device, but do not exclude the presence or addition of one or more other compositions, steps, methods, articles or devices. In addition, when describing the embodiments of the present application, the use of "preferred", "preferably", "more preferrably", etc. refers to an embodiment of the present invention that can provide certain beneficial effects under certain circumstances. However, other embodiments may also be preferred under the same or other circumstances. In addition, the expression of one or more preferred embodiments does not imply that other embodiments are not available, nor is it intended to exclude other embodiments from the scope of the present invention.
  • In order to solve the above technical problems, the present invention provides a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    1. a. dissolving a polyacrylonitrile raw material in a polar solvent under mechanical stirring to obtain a uniform spinning solution;
    2. b. making the polyacrylonitrile solution in the step a into a polyacrylonitrile nonwoven fabric in an electrospinning machine;
    3. c. cutting the nonwoven fabric in the step b into slender strips with a width of 0.5 to 6 cm;
    4. d. drafting the slender strips in the step c in a water bath at 80 to 95°C with a draft ratio of 2 to 5 times, then drafting in air at 110 to 150°C with a draft ratio of 3 to 10 times to obtain a fiber bundle with highly oriented internal fibers;
    5. e. twisting the fiber bundle in the step d to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers with a length of not less than 2000 meters.
    Step a
  • The objective of step a is to prepare a polymer solution suitable for electrostatic spinning, and because there are a large number of polar cyano groups in polyacrylonitrile, selecting a suitable polar solvent helps to prepare a spinning solution with suitable concentration and adjustable viscosity.
  • Step a. dissolving a polyacrylonitrile raw material in a polar solvent under mechanical stirring to obtain a uniform spinning solution.
  • In some preferred embodiments, the polyacrylonitrile raw material and the polar solvent are added together in a stainless steel reactor and dissolved under mechanical stirring to obtain a uniform polyacrylonitrile solution for spinning.
  • The polyacrylonitrile raw material in the present invention is not particularly limited, and may be commercially available, and the CAS number is 25014-41-9.
  • In some embodiments, the polar solvent in step a is selected from one or more of N, N-dimethylformamide (CAS number: 68-12-2), N-methylpyrrolidone (CAS number: 872-50-4), dimethyl sulfoxide (CAS No. 67-68-5) and N, N-dimethylacetamide (CAS No. 127-19-5).
  • Both dimethyl sulfoxide and N-methylpyrrolidone are good solvents for dissolving polyacrylonitrile, and dimethyl sulfoxide is non-toxic, but both have boiling points above 200°C, and the spun yarns are not easy to dry and have serious adhesion to each other. N, N-dimethylformamide has the lowest boiling point among several listed solvents and has the best solubility, while N, N-dimethylacetamide has relatively low solubility, but has the advantage of low toxicity which can be compounded with N, N-dimethylformamide to make a mixed solvent for spinning.
  • In some preferred embodiments, the polar solvent in the step a is N, N-dimethylformamide and/or N, N-dimethylacetamide; further preferably, the N, N-Dimethylformamide and N, N-dimethylacetamide; further, the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide is 4: 1.
  • The concentration of the spinning solution determines the viscosity of the solution, if the viscosity is too large, the electrostatic force needs to overcome a greater surface tension, making the spinning diameter too large or even impossible to spin; and too small viscosity will make the spinning too thin, insufficient strength, or beads may appear on the spinning. In some preferred embodiments, the mass concentration of the solution in the step a is 12 to 22%; further preferably, the mass concentration of the solution in the step a is 13 to 18%.
  • In some preferred embodiments, the absolute viscosity of the solution in the step a is 1.5 to 5 Pa.S; further preferably, the absolute viscosity of the solution in the step a is 2 to 4 Pa.S.
  • On the one hand, appropriate dissolution temperature can speed up the dissolution rate and improve the processing efficiency, on the other hand can reduce the solubility of the gas in the solution, and remove the gas from the solution. In some preferred embodiments, the dissolution temperature in the step a is 30 to 55°C. and the stirring time is 4 to 10 hours; further preferably, the dissolution temperature in the step a is 38 to 48°C. and the stirring time is 6 to 9 hours.
  • Step b
  • The objective of the step b is to make polyacrylonitrile from solution into a nonwoven fabric, in this process, the polymer solution is sprayed into a strong electric field. Under the action of the electric field, the sprayed droplets change from spherical to Taylor cone, from the tip of which a tiny jet is extended, and after running for a certain distance, the jet is solidified into fiber filaments, which are collected by a stainless steel mesh belt to obtain a nonwoven fabric.
  • Step b. making the polyacrylonitrile solution in the step a into a polyacrylonitrile nonwoven fabric in an electrospinning machine.
  • In some preferred embodiments, the polyacrylonitrile solution is injected into the spinning device of an electrospinning machine, spraying spun in a high-voltage electric field, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric.
  • The magnitude of the voltage of the electric field will affect the shape of the sprayed droplets. Too small voltage can not make the spherical droplets of the spinneret form a Taylor cone, and too large voltage will cause the formed Taylor cone to retreat or even back into the spinneret, resulting a large number of beads appeared in the spinning fibers. In some preferred embodiments, the DC voltage of the high-voltage electric field in the step b is 30 to 50 kV; further preferably, the DC voltage of the high-voltage electric field in the step b is 40 to 45 kV.
  • The distance between the spinneret and the stainless steel mesh belt collector requires to ensure that the jet can be solidified during running without adhesion, and improper receiving distance will cause beads appeared in the spinning fibers. In some preferred embodiments, the distance between the spinneret and the stainless steel mesh belt collector in the step b is 25 to 55 cm; further preferably, the distance between the spinneret and the stainless steel mesh belt collector is 28 to 35 cm.
  • The travel speed of the stainless steel mesh belt can affect the pore size and thickness of the nonwoven fabric, which in turn affects the strength of the filament yarn processed from the nonwoven fabric. In some preferred embodiments, the travel speed of the stainless steel mesh belt in the step b is 1 to 5 m/min; further preferably, the travel speed of the stainless steel mesh belt is 2 to 4 m/min.
  • In some preferred embodiments, the diameter of the spinning in step b is 100-1500 nm; further preferably, the diameter of the spinning in the step b is 100 to 500 nm.
  • Step c
  • The objective of the step c is to pretreat the polyacrylonitrile nonwoven fabric into a form suitable for further processing.
  • Step c: cutting the nonwoven fabric in the step b into slender strips with a width of 0.5 to 6 cm.
  • The width of the cut strip will affect the subsequent further processing, and too narrow cut strip is not conducive to continuous production, making the resulting yarn easily broken, and it is impossible to achieve the ideal length to obtain a filament yarn; while too wide cut strip is difficult to process to obtain a fiber bundle with highly oriented internal fibers. In some preferred embodiments, the width of the slender strip in the step c is 0.5 to 6 cm; further preferably, the width of the slender strip is 2 to 5.5 cm.
  • Step d
  • The objective of the step d is, on the one hand, to obtain a fiber bundle length sufficient to produce continuous filament yarns through drafting, and on the other hand, to change the degree of orientation of the internal fibers, making the strength of the fiber bundle in the orientation direction increased greatly .
  • Step d: drafting the slender strips in the step c in a water bath at 80 to 95°C with a draft ratio of 2 to 5 times, then drafting in air at 110 to 150°C with a draft ratio of 3 to 10 times to obtain a fiber bundle with highly oriented internal fibers.
  • In some preferred embodiments, the water bath draft and air draft in the step d are 5-roll drafts.
  • In some preferred embodiments, the unwinding speed of the water bath draft is 2 to 8 m/min; further preferably, the unwinding speed of the water bath draft is 4 to 7 m/min.
  • In some preferred embodiments, the unwinding speed of the air draft is 3 to 8 m/min; further preferably, the unwinding speed of the air draft is 4 to 7 m/min.
  • In some preferred embodiments, the fiber orientation degree of the fiber bundle in the step d is 90% to 95%.
  • Step e
  • The objective of the step e is to twist the fiber bundle into a filament yarn. After twisting, the outer fiber and the inner fiber squeeze each other to generate pressure, making the yarn obtain frictional force along the fiber length, and the fiber strip is longitudinally fixed, and the fiber after yarn formation has improved properties such as strength, elongation, gloss, and feel.
  • Step e: twisting the fiber bundle in the step d to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers with a length of not less than 2000 meters.
  • In some preferred embodiments, the unwinding speed of twisting in the step e is 5 to 50 m/min; further preferably, the unwinding speed of twisting is 20 to 40 m/min.
  • In some preferred embodiments, the twist degree of twisting in the step e is 500 to 1500 twist/m; further preferably, the twist degree of twisting in the step e is 800 to 1200 twist/m.
  • Compared with other fibers, the strength of polyacrylonitrile nanofibers is lower. In terms of the original excellent properties of polyacrylonitrile such as weather resistance and warmth retention, the strength of polyacrylonitrile fiber after high drafting is further improved, which broadens its range of application. After the fiber is drafted and twisted, filament yarn can be produced continuously, which in turn can be used for pure or blended with other fibers to weave alight-weight, warm, soft, and comfortable high-grade fabric.
  • Examples
  • The technical solutions of the present invention will be described in detail below through the examples, but the protection scope of the present invention is not limited to the examples.
  • Example 1
  • Example 1 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric. The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 2
  • Example 2 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and N, N-dimethylformamide in a stainless steel reaction reactor under mechanically stirring, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric. The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 3
  • Example 3 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 4
  • Example 4 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 2 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 5
  • Example 5 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4:1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 5.5 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 6
  • Example 6 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 5 times to obtain a fiber bundle of electrospun polyacrylonitrile;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 7
  • Example 7 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 2 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 8
  • Example 8 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 88°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 5 times, then 5-roll drafting in air at 135°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 10 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 9
  • Example 9 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 80°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 110°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Example 10
  • Example 10 provided a method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, comprising the following steps:
    • dissolving a polyacrylonitrile raw material and a mixed solvent composed of N, N-dimethylformamide and N, N-dimethylacetamide in a stainless steel reaction reactor under mechanically stirring, and the mass ratio of N, N-dimethylformamide and N, N-dimethylacetamide was 4: 1, the dissolution temperature was 43°C., the stirring time was 8 hours. and the mass concentration of the obtained polyacrylonitrile solution for spinning was 15%;
    • injecting the solution obtained in the step a into the spinning device of an electrostatic spinning machine, spraying spun in a high-voltage electric field with a DC voltage of 42 kV, and collected with a stainless steel mesh belt to obtain an electrospun polyacrylonitrile nonwoven fabric, The distance between the spinneret and the stainless steel mesh belt collector was 33 cm, the travel speed of the stainless steel mesh belt was 3 m/min, and the diameter of the spinning was 150 nm;
    • cutting the nonwoven fabric in the step b into slender strips with a width of 4 cm;
    • 5-roll drafting the slender strips in the step c in a water bath at 95°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 3 times, then 5-roll drafting in air at 150°C with an unwinding speed of twisting of 6 m/min and a draft ratio of 6 times to obtain a fiber bundle of electrospun polyacrylonitrile with highly oriented internal fibers;
    • twisting the fiber bundle in the step d to more than 2000 meters, the unwinding speed was 25 m/min, and the twist degree was 900 twist/m to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers.
    Performance evaluation
  • The continuous filament yarns of electrospun polyacrylonitrile nanofibers obtained in examples 1 to 10 were tested for metric count, tensile strength, Young's modulus, and elongation at break.
  • Metric count,: 1000 meters of yarn was weighed its gram weight, and the metric count = 1000/gram weight. The results were shown in Table 1.
  • Tensile strength, Young's modulus, elongation at break: tested with an electronic universal tensile machine. The results were shown in Table 1. Table 1
    Metric count Tensile strength Young's modulus Elongation at break
    Example 1 740 15 cN/dtex 298 cN/dtex 11%
    Example 2 720 14.5 cN/dtex 290 cN/dtex 12%
    Example 3 660 12 cN/dtex 246 cN/dtex 19%
    Example 4 760 3 cN/dtex 84 cN/dtex 12%
    Example 5 700 13 cN/dtex 260 cN/dtex 14%
    Example 6 450 6 cN/dtex 108 cN/dtex 32%
    Example 7 520 11.5 cN/dtex 223 cN/dtex 27%
    Example 8 800 8 cN/dtex 130 cN/dtex 10%
    Example 9 630 10 cN/dtex 194 cN/dtex 22%
    Example 10 600 9.5 cN/dtex 172 cN/dtex 17%
  • It can be known from the comparison of examples 1 to 10 that the method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers can produce a high count filament yarn with a length of more than 2000 meters, while improving the mechanical properties of the polyacrylonitrile fiber.
    Finally, it is pointed out that the foregoing is only preferred exemplary embodiments of the present invention and is not intended to be limiting of the present invention, and any modifications, equivalent substitutions, improvements and the like within the spirit and principles of the present invention are intended to be embraced by the protection range of the present invention.

Claims (10)

  1. A method for preparing a continuous filament yarn of electrospun polyacrylonitrile nanofibers, the method comprising the following steps:
    a. dissolving a polyacrylonitrile raw material in a polar solvent under mechanical stirring to obtain a uniform spinning solution;
    b. making the polyacrylonitrile solution in the step a into a polyacrylonitrile nonwoven fabric in an electrospinning machine;
    c. cutting the nonwoven fabric in the step b into slender strips with a width of 0.5 to 6 cm;
    d. drafting the slender strips in the step c in a water bath at 80 to 95°C with a draft ratio of 2 to 5 times, then drafting in air at 110 to 150°C with a draft ratio of 3 to 10 times to obtain a fiber bundle with highly oriented internal fibers;
    e. twisting the fiber bundle in the step d to obtain a continuous filament yarn of electrospun polyacrylonitrile nanofibers with a length of not less than 2000 meters.
  2. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that the polar solvent in the step a is selected from one or more of N, N-dimethylformamide, N-methylpyrrolidone, dimethyl sulfoxide, N, N-dimethylacetamide.
  3. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that the water bath draft and the air draft in the step d are 5-roll drafts.
  4. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that the unwinding speed of the water bath draft in the step d is 2 to 8 m/min.
  5. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that an unwinding speed of the air draft in the step d is 3 to 8 m/min.
  6. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that the fiber orientation degree of the fiber bundle in the step d is 90% to 95%.
  7. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that the unwinding speed of twisting in the step e is 5 to 50 m/min.
  8. The method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 1, characterized in that the twist degree of twisting in the step e is 500 to 1500 twist/m.
  9. A continuous filament yarn of electrospun polyacrylonitrile nanofibers, which is prepared by the method for preparing the continuous filament yarn of electrospun polyacrylonitrile nanofibers according to any one of claims 1 to 8.
  10. The continuous filament yarn of electrospun polyacrylonitrile nanofibers according to claim 9, which can be used for pure or blended spinning to weave a light-weight and warm high-grade fabric.
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