KR101811650B1 - Manufacturing method of nanofiber fabric for bed clothes - Google Patents
Manufacturing method of nanofiber fabric for bed clothes Download PDFInfo
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- KR101811650B1 KR101811650B1 KR1020160028512A KR20160028512A KR101811650B1 KR 101811650 B1 KR101811650 B1 KR 101811650B1 KR 1020160028512 A KR1020160028512 A KR 1020160028512A KR 20160028512 A KR20160028512 A KR 20160028512A KR 101811650 B1 KR101811650 B1 KR 101811650B1
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
- D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
- D04H1/728—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by electro-spinning
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- 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
- D01D5/0007—Electro-spinning
- D01D5/0015—Electro-spinning characterised by the initial state of the material
- D01D5/003—Electro-spinning characterised by the initial state of the material the material being a polymer solution or dispersion
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- 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
- D01D5/0007—Electro-spinning
- D01D5/0061—Electro-spinning characterised by the electro-spinning apparatus
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/425—Cellulose series
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4282—Addition polymers
- D04H1/4318—Fluorine series
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/4334—Polyamides
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/435—Polyesters
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/4358—Polyurethanes
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
- D04H1/498—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres entanglement of layered webs
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2503/00—Domestic or personal
- D10B2503/06—Bed linen
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2503/00—Domestic or personal
- D10B2503/06—Bed linen
- D10B2503/062—Fitted bedsheets
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Dispersion Chemistry (AREA)
- Nonwoven Fabrics (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Abstract
The present invention relates to a method for producing a bedding nanofiber fabric. The present invention relates to a nanofibrous web, in which a support or a substrate on which a nanofiber web is laminated is rotated so that two or more bottom-up and bottom-down electrospinning devices are alternately arranged on the same surface successively, The present invention relates to a bedding-type nano-fiber fabric prepared by laminating a plurality of nano-sized bed-type nanofibers, and the manufacturing process can be simplified and the manufacturing time can be reduced.
Description
The present invention relates to a method for producing a bedding-type nano-fiber fabric, which is a structure in which nanofibers are fabricated by arranging two or more bottom-up and top-down electrospinning devices alternately and the nanofiber web is laminated on the substrate.
Generally, the size of house dust mite is about 100-300 ㎛, but the excrement and dead body of house dust mites are about 40 ㎛ or less in size and are very small because they are visually distinguished. There is a problem that the possibility of infiltration into the bedding is increased and the laundry is not removed by the washing. In the case of house dust mites, there is a problem of causing diseases such as atopy, rhinitis and asthma by creating a harmful environment inside the house. Mite excreta or carcass debris can cause ailments if it enters a person's respiratory tract or touches the skin. In the case of bedding, especially quilt, it is necessary to manage bedding cleanly because it provides an environment suitable for propagation of bacteria such as ticks.
For this purpose, efforts have been made to prevent the propagation of bacteria by using nanofibers on bedding. There has been a problem in that production speed and production amount according to the bottom-up type are lowered when nanofibers are produced by the conventional bottom-up electrospinning apparatus in manufacturing bedding nanofiber fabrics used for bedding.
In addition, in the case of a technique for spinning conventional nanofibers, since it is limited to a small-scale working line focused on a laboratory, there is a demand for a technique of spinning nanofibers by dividing a spinning zone and using a unit concept.
SUMMARY OF THE INVENTION The present invention has been conceived to solve the problems as described above, and it is an object of the present invention to provide an apparatus and a method for manufacturing an electrostatic latent electrostatic precipitator by alternately providing a bottom- Which is an advantage of a bottom-up electrospinning apparatus, and a mass production method which is an advantage of a top-down electrospinning apparatus, which is advantageous of a bottom-up electrospinning apparatus, And a method for producing the same.
According to a preferred embodiment of the present invention, there is provided a method of manufacturing a semiconductor device, comprising: preparing a support; Forming a nanofiber web on the lower surface of the support by electrospinning a polymer spinning solution with a bottom-up electrospinning device; And a step of continuously laminating a nanofiber web by electrospinning a polymer spinning solution with a top-down electrospinning device on a nanofiber web laminated on the support, wherein the polymer spinning solution is electroless- And a step of laminating a nanofiber web by electrospunning a polymer spinning solution with a top-down electrospinning device is alternately formed in two or more stages, And a step of rotating the lower surface of the support body by 180 degrees to the upper surface while passing the rotating device between the step of forming the fibrous web and the step of laminating the fibrous web.
According to another preferred embodiment of the present invention, the total basis weight of each nanofiber web is less than 0.1 g / m < 2 > and less than 1.0 g / m < 2 >, the support is a thermoplastic polyurethane base, The polymer spinning solution is the same material and is composed of one or more selected from the group consisting of polyurethane, polyvinylidene fluoride and nylon.
According to another preferred embodiment of the present invention, each of the polymer spinning solution includes an antibacterial substance, and each of the nanofiber webs has a different basis weight on the same plane in the longitudinal direction or the width direction of the support, Further comprising the step of separating the support on which the nanofiber webs are laminated from the support and separately positioning and laminating the support on the substrate after the successive lamination step. to provide.
According to another preferred embodiment of the present invention, the polymeric spinning solution is electrospun through a temperature controller at a temperature of 45 to 120 ° C.
As described above, according to the present invention having the above-described structure, the support on which the nanofiber web is laminated is rotated, and a nanofiber web is continuously produced on the same surface by using an up-down and down- It is possible to simplify the manufacturing process and reduce the manufacturing time.
In addition, since the rotating device for rotating the support is installed between the electrospinning devices, the space utilization of the electrospinning device can be installed in a horizontally or vertically arranged layered structure on the plane, It is easy and at the same time, there is a margin in the installation space. In other words, it is possible to install and operate the electrospinning device in a narrow space and to produce a mass production of the bedding nano fiber fabric.
1 is a side view schematically showing an apparatus for producing nanofibers according to the present invention,
2 is a plan view schematically showing a nozzle block installed in each electrospinning device of the nanofiber manufacturing apparatus of the present invention,
3 is a front sectional view schematically showing a state in which a heating wire for temperature control is installed in a nozzle block installed in each electrospinning device of the nanofiber manufacturing apparatus of the present invention,
4 is a sectional view taken along line AA in Fig. 3,
5 and 6 are cross-sectional views schematically showing a flip device used as an embodiment of a rotating device of a nanofiber manufacturing apparatus of the present invention,
7 is a plan view showing a state in which the tube body of the nozzle block of the present invention is turned on and off in the CD direction,
FIG. 8 is a plan view showing a process of electrospinning of a nozzle in a nozzle block, as shown in FIG. 7,
FIG. 9 is a plan view showing a process of electrospinning of a nozzle in a nozzle block in the nozzle block according to an embodiment of the present invention,
10 is a side view schematically showing the arrangement of the apparatus for producing nanofibers of the present invention in the vertical direction,
Fig. 11 is a bird's-eye view schematically showing the arrangement of a case where the apparatus for producing nanofibers of the present invention is arranged in a U-shape with respect to the horizontal direction.
Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. The present invention is not limited to the scope of the present invention, but is merely an example, and various modifications can be made without departing from the technical spirit of the present invention.
2 is a plan view schematically showing a nozzle block installed in each electrospinning apparatus of the nanofiber manufacturing apparatus of the present invention. FIG. 3 is a cross- FIG. 4 is a cross-sectional view taken along the line AA in FIG. 3, and FIGS. 5 and 6 are cross-sectional views taken along line AA 'in FIG. FIG. 7 is a cross-sectional view schematically showing a flip device 20-1, which is an embodiment of a
As shown in the drawing, an
The bottom-up
According to the structure as described above, the
On the other hand, the nozzle blocks 13 and 33 in which the
In an embodiment of the present invention, a temperature regulating device 60 consisting of a hot line is spirally arranged on the inner circumference of the tubular body of the
Meanwhile, a bottom-up
In the present invention, although the two bottom-
The
As the above substrate, it is possible to use cellulose, a synthetic substrate (synthetic substrate), a polyethylene terephthalate substrate, a bicomponent substrate, a thermoplastic polyurethane (TPU) substrate and the like. The two-component base material is most preferably polyethylene terephthalate in which two components having different melting points are combined. The polyethylene terephthalate two-component substrate may be classified into a sheath-core type, a side-by-side type, a C-type, and the like. In the case of the sheath-core type two-component substrate, the sheath portion is a low melting point polyethylene terephthalate, and the core portion is made of general polyethylene terephthalate. Wherein the sheath portion is about 10 to 90 wt%, and the core is about 90 to 10 wt%. The sheath portion acts as a thermal binder to form the outer surface of the binder fiber, has a melting point of about 80 to 150 占 폚, and the core has a melting point of about 160 to 250 占 폚. The CIS type heterogeneous base material used as an embodiment in the present invention includes an amorphous polyester copolymer in which a melting point is not exhibited by a conventional melting point analyzer in the sheath portion and preferably a relatively high melting point component Is a thermally adhesive composite fiber to be used.
The polyester copolymer contained in the sheath portion is a copolyester in which 50 to 70 mol% is a polyethylene terephthalate unit. As the copolymerizable acid component, isophthalic acid is preferably used in an amount of 30 to 50 mol%, but any other conventional dicarboxylic acid may be used.
As a high melting point component used as a core component, a polymer having a melting point of 160 ° C or higher is suitable. Examples of the high melting point component include polyethylene terephthalate, polybutylene terephthalate, polyamide, polyethylene terephthalate copolymer and polypropylene.
The basis weight of the two -component base is preferably 10 to 50 g / m 2 , and the basis weight of the polyethylene terephthalate base is preferably 50 to 300 g / m 2 .
In the present invention, a thermoplastic polyurethane (TPU) is preferably used as the most preferable example. The TPU substrate is preferably produced in a meltblown manner.
First, the polyurethane is a polymer of a urethane bond formed by the reaction of a polyisocyanate and a polyalcohol. Polyurethane is excellent in elasticity, abrasion resistance, and processability, and is widely used in industrial, consumer products, and parts. Since the properties of polyurethane vary depending on the type of polyurethane, selection of a product suitable for the application is important.
The polyurethane is classified into two types, thermoplastic polyurethane and thermosetting polyurethane. The thermoplastic polyurethane has excellent characteristics such as strength, formability, chemical resistance, oil resistance and wear resistance. BACKGROUND ART Flexible nonwoven fabrics made of thermoplastic polyurethane (hereinafter referred to as "TPU") have been used for applications including clothing, sanitary materials and sporting goods materials due to their high elasticity, low residual strain and excellent air permeability
The process for producing the thermoplastic polyurethane is well known. That is, it is prepared by reacting a linear polyol containing a hydroxy end group such as a polyester polyol or a polyether polyol with a diisocyanate compound containing an isocyanate group at both terminals, and optionally, a chain extender, a monoamine compound Terminal stopping agents, and other additives.
Examples of the polyol include various diols comprising a linear homo or copolymer such as a polyester diol, a polyether diol, a polyester amide diol, a polyacryl diol, a polythioester diol, a polythioether diol, a polycarbonate diol, ≪ / RTI > may be used. More specific examples include polyalkylene ether glycols such as polyoxyethylene glycol, polyoxypropylene glycol, polytetramethylene ether glycol, copolymer polyether glycol composed of tetramethylene group and 3-methyl tetra ketylene group.
As the diisocyanate compound serving as a hard segment, an aromatic, aliphatic or alicyclic diisocyanate is used, for example, 4,4'-diphenyl ketadiisocyanate, 1,3- and 1,4-cyclohexylene diisocyanate, 1,6-hexamethylene diisocyanate, trimethylene diisocyanate, tetramethylene diisocyanate, isophorone diisocyanate, and the like, but are not limited thereto.
Examples of the chain extender include a diamine compound or a diol compound. Examples of the chain extender include a diamine compound such as methylene diamine, ethanol diamine, 1,2-propylene diamine and the like, and a diamine compound such as ethylene glycol, 1,3-propanediol, , Neopentyl glycol, and the like, but are not limited thereto.
Examples of the terminal terminating agent include monoamine compounds such as monoethanolamine, diethanolamine and diisopropylamine.
On the other hand, the number average molecular weight of the thermoplastic polyurethane is preferably 1,000 to 100,000.
In the present invention, such a thermoplastic polyurethane is used as a base material. The nonwoven fabric is produced by preparing a web (a state in which fibers are repeatedly laminated) and entangling the fibers physically and chemically together.
Typical nonwoven fabrication processes involve web formation and web bonding processes. The general process is used only for single-fiber nonwovens, and this process is not necessary because longwoven nonwovens use filaments by spinning. In the case of non-woven fabric, it is put in a compressed bale state, so that the nonwoven fabric must undergo the process of compressed fibers. The formation process of the web is a necessary process for forming the nonwoven fabric. The dry nonwoven fabric forms the web in the air, whereas the wet nonwoven fabric disperses the fibers to obtain the web. Therefore, in the dry nonwoven fabric, the arrangement of the fibers is mostly directional, but the wet nonwoven fabric has a random irregular arrangement of the fibers. However, the development of a random card machine for dry nonwovens also makes it possible to obtain a web having no directionality depending on its application.
As a method of forming the web, a spun bond method using long fibers produced by dissolving radiation from raw pellets, a dry method of forming a web by arranging short fibers in a predetermined direction in a card machine or the like, And a wet method in which the water is homogeneously dispersed and drained to form a web.
Methods for entangling the fibers include a thermal bond method in which a thermally soluble fiber is mixed with a web and a thermal roll is used, a chemical bond method in which a binder is bonded (adhered fat), a barb of a needle A meltblown method capable of forming webs randomly by impacting filaments with high-pressure air at the time of producing fibers, and capable of producing a web having a diameter of 0.5 to 30 microns, etc. .
Among them, the thermoplastic polyurethane base used in the present invention is preferably produced by the meltblown method, the spunbond method and the needle punch method among the above methods. The principle of the meltblown method is a melt spinning method using a thermoplastic resin, in which a high-temperature and high-pressure airflow is introduced into the outlet of the spinning nozzle to stretch and open the fibers, and then the fibers are accumulated on a collecting conveyor. The nonwoven fabric by this method has an advantage of being excellent in flexibility, impermeability and insulation.
On the other hand, the spunbond method is a method in which a raw material is spun and self-bonded by heat to form a nonwoven fabric. It is a technology to form a web by spinning self-adhesive polypropylene or polyethylene terephthalate by heat, and it has an advantage of easy fabric design.
In addition, in the case of the needle punching method, fibers are physically manufactured by combining webs using special needles, and it is possible to diversify the thickness of the product by the number of punching of needles and the density of needles.
The thermoplastic polyurethane nonwoven fabric produced by such a nonwoven fabric manufacturing method is preferably used as the base material used in the present invention. The basis weight of the base material is preferably 10 to 150 g / m < 2 >. If the basis weight is less than 10 g / m < 2 >, the physical properties of the base material are poor. If the basis weight is more than 150 g / m &
The thermoplastic polyurethane nonwoven fabric can be hydrophobic or hydrophilic, can be introduced in color, and can be partially melted in a high-temperature laminating environment due to its thermoplastic characteristics, so that the thermoplastic polyurethane non- There is a possible advantage.
The bottom-up
On both sides of the
In the meantime, the present invention is characterized in that a
5 and 6 are cross-sectional views schematically showing a flip device 20-1 used as an embodiment of a rotating device. 5 is a cross-sectional view showing an initial operation of the flip device 20-1, and FIG. 6 is a cross-sectional view showing a process of the flip device 20-1 in the latter stage of operation.
The flip device 20-1 used as an embodiment of the rotating device is formed as a cylindrical body having a hollow inside and is provided at its central portion with both ends of the
The one end and the other end of the support inserted into the
In the present invention, the flip device 20-1 is used as the
The polymer spinning solution filled in the spinning solution
The nanofibers produced while passing through the bottom-up
According to an embodiment of the present invention, the voltage of the bottom-up electrospinning device is higher than the voltage of the bottom-up electrospinning device so that the diameter of the nanofibrous web produced by the bottom- It is possible to make the nanofibrous web narrower than the diameter of the nanofibrous web produced by the method.
Meanwhile, it is also possible to fill the spinning liquid
However, in the present invention, the polymer solution used in the bottom-up
Here, the polymer spinning solution is not particularly limited, and examples thereof include polypropylene (PP), polyethylene terephthalate (PET), polyvinylidene fluoride, nylon, polyvinylacetate, polymethylmethacrylate, (PAN), polyurethane (PUR), polybutylene terephthalate (PBT), polyvinyl butyral, polyvinyl chloride, polyethyleneimine, polyolefin, polylactic acid (PLA), polyvinyl acetate (PEN), polyamide (PA), polyvinyl alcohol (PVA), polyethyleneimide (PEI), polycaprolactone (PCL), polylactic acid glyceric acid (PLGA), silk, cellulose and chitosan. (PP) materials and heat-resistant polymer materials such as polyamide, polyimide, polyamideimide, poly (meta-phenylene isophthalamide), polysulfone, polyether ketone, polyether Aromatic polyesters such as polyethylene terephthalate, polyethylene terephthalate and polyethylene naphthalate, polytetrafluoroethylene, polydiphenoxaphospazene, polybis [2- (2-methoxyethoxy) phosphazene] , A polyurethane copolymer including polyurethane and polyether urethane, cellulose acetate, cellulose acetate butyrate, cellulose acetate propionate, and the like, are preferably used in a commercial manner. More preferably, one or more selected from the group consisting of polyurethane, polyvinylidene fluoride and nylon is preferably used.
The polymer spinning solution is a solution prepared by dissolving a polymer, which is a synthetic resin material capable of electrospinning, in a suitable solvent, and the type of solvent is not limited as long as it can dissolve the polymer. For example, methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, isopropyl, n-butyl, isobutyl, sec-butyl, Isobutyl alcohol, isopropyl alcohol, methyl alcohol, ethanol, aliphatic compounds such as hexane, tetrachlorethylene, acetone, and glycol groups such as propylene glycol, diethylene glycol, isobutyl ketone, methyl ethyl ketone, aliphatic hydroxyl group, m- Ethylene glycol, and halogen compounds such as trichlorethylene, dichloromethane, aromatic compounds toluene, xylene, alicyclic compounds such as cyclohexanone, cyclohexane and esters such as n-butyl acetate, ethyl acetate, aliphatic ether Butyl cellosolve, acetic acid 2-ethoxy ethanol, 2-ethoxy ethanol, amide dimethyl formamide, dimethylacetamide, etc. And, it is possible to use a mixture of a plurality kinds of solvents. The polymer spinning solution preferably contains, but is not limited to, an additive such as a conductivity improver.
In the present invention, it is preferable that an additive such as an antimicrobial agent is contained in the polymer spinning solution. When the polymer spinning solution is electrospun, the antimicrobial agent is spun together to prevent the problem of microbial growth which is a problem of the bedding nano fiber fabric.
Antimicrobial agents can be broadly divided into organic antimicrobial agents and inorganic antimicrobial agents. Organic antimicrobial agents are mainly in liquid form and are added to products that require antimicrobial activity in a short time. Organic antimicrobial agents are temporarily higher in antibacterial activity than inorganic antibacterial agents, but have a very short persistence of antibacterial activity. In addition, there are concerns about generation of resistant bacteria and acute toxicity, resulting in problems in human safety. Due to these problems, the use area of organic antibacterial agents is being reduced.
Inorganic antibacterial agent is a product made by replacing metal ions such as silver, zinc, copper, etc., which are antibacterial effects on minerals such as zeolite, calcium phosphate, zirconium phosphate and silica gel, and is currently used in various fields such as plastic products, paper and textile . Inorganic antimicrobial agents have a lower temporary antimicrobial activity than organic antimicrobial agents, but have high human safety, do not show resistant bacteria, and have a semi-persistent period of antimicrobial use.
These inorganic antimicrobial agents mainly include zeolite, calcium phosphate and zirconium phosphate. Most of them are zeolite inorganic antibacterial agents.
Inorganic antibacterial agents based on calcium phosphate are disadvantageous in that the concentration of substitution metal ions is lower than that of zeolite inorganic antibacterial agents, and the antibacterial activity is lower than that of zeolite agents. Inorganic antibacterial agents of zirconium phosphate also have low antibacterial activity, high unit cost, And has a disadvantage of high hardness.
In contrast, zeolite-based inorganic antimicrobial agents have many advantages such as no discoloration problem, high antibacterial activity and low particle hardness compared with other antimicrobial agents, and are excellent in application method and safety problem since they are the most widely applied antimicrobial agents It is an antibacterial agent.
It is also possible to prepare a bedding nanofiber fabric having antimicrobial properties by adding the antibacterial agent as described above to the polymer spinning solution.
In the present invention, the polymer spinning solution filled in the spinning solution
Each of the nozzle blocks 13 and 33 of the present invention includes a
Here, the
At this time, a supply pipe adjusting means (not shown) is provided in the supply piping which is communicated to the
In this way, valves are respectively provided in the supply liquid piping leading to the
That is, when the polymer solution is supplied from the spinning solution
By using the structure as described above, the waste liquid
That is, each of the
The radiation amount regulating means is constituted by a valve. In this way, the supply of the polymer spinning solution supplied to the
In the present invention, if the amount of the spinning solution of the polymer spinning solution is easily controlled and controlled after the spinning amount control means is provided as a valve but is supplied to the
In the present invention, a valve is provided in the supply piping so that the
The bedding nanofiber fabric end manufactured according to the present invention is characterized in that it has a different basis weight in the width direction, that is, in the CD direction or in the lateral direction, and is electrospun electrically deposited in the longitudinal direction, that is, in the MD direction. The CD direction is the cross direction, which means the direction perpendicular to the MD direction (Machine Direction). The MD direction is the longitudinal direction / longitudinal direction, and the CD direction is the width direction / transverse direction.
Basis Weight or Grammage, on the other hand, is defined as the mass per unit area, that is, the preferred unit, grams per square meter (g / m 2).
In the production of the bedclothes nanofiber fabric of the present invention, the basis weight of the total stacked nanofiber web is preferably 0.1 g / m 2 or more and 20.0 g / m 2 or less, more preferably 0.1 g / m 2 or more and less than 1.0 g / m 2 . Here, when the basis weight of the total nanofiber web is less than 0.1 g / m < 2 > or 1.0 g / m < 2 >, there is a disadvantage in that mechanical properties and antibacterial effect are not large.
7 is a plan view showing a state in which the
A laminating apparatus for laminating each of the nanofiber webs and the
The bottom-up
That is, the rotary device is characterized in that the support rotates 180 degrees or vertically rotates in the U-turn direction by the flip device.
Meanwhile, in an embodiment of the present invention, a
A feeding roller for feeding another substrate (not shown) is provided on the upper side of the
Hereinafter, a method of fabricating the bedding nano fiber fabric through the operation of the nanofiber manufacturing apparatus of the present invention will be described.
First, the
On the other hand, the
Here, the spinning liquid to be filled in the spinning liquid
As described above, the
The
The supporting
The high voltage of the voltage generator is generated in the
Each of the voltage generators has a structure similar to that of a general electrospinning device and generates a high voltage in the
On the other hand, the spinning liquid to be filled in the spinning liquid
The polymer constituting the first nanofiber web and the second nanofiber web is preferably one selected from the group consisting of polyurethane, polyvinylidene fluoride and nylon. Particularly, when a polyurethane is used as a nanofiber web and a thermoplastic polyurethane base is used as a base material, due to the similarity of materials of the base material and the nanofiber web, separation between the base material and the nanofiber is not easily caused by the laminating process There is an advantage in that the thermoplastic polyurethane base acts as an adhesive layer even if a raw material used for cellulose or bedding is placed on the outer surface of the substrate and laminated together.
At this time, the conveyance of the
In the present invention, it is preferable that the bottom-up
That is, the rotary device is characterized in that the support rotates 180 degrees or vertically rotates in the U-turn direction by the flip device.
As described above, by repeating the process of successively laminating the nanofibers on one surface of the
In the present invention, the spinning liquid
That is, the polymer solution sprayed from the bottom-up
As described above, the nanofibers are manufactured by the
Here, the
Also, it is possible to further include an air
In the case of the bedding nanofiber fabric prepared according to the present invention, it is preferable that the fabric is used by placing and laminating cellulose, cloth, cloth, knitted fabric, nonwoven fabric, scrim fabric and the like. In the case of cellulose, cloth, cloth, knitted fabric, nonwoven fabric, scrim fabric and the like which can be laminated on the fabric, it is preferable that the basis weight is 100 to 400 g / m 2.
While the present invention has been particularly shown and described with reference to specific embodiments thereof, it will be understood by those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the invention as defined in the appended claims. Anyone with it will know easily.
[Example 1]
13% by weight of polyurethane (Pellethane 2363-80AE from DOW, USA) was dissolved in 87% by weight of NN-dimethylacetamide (DMAc) to prepare a polymer solution having a concentration of 13% And the same polymer spinning solution was provided in the raw material tank of the top-down electrospinning device at the rear end. Thereafter, the first polyurethane nanofiber web was laminated on a TPU base material (IOH10UM4 manufactured by Bluecher) having a basis weight of 30 g / m < 2 > in a bottom-up electrospinning device positioned at the front end, The laminate is rotated 180 degrees. The second polyurethane nanofiber web is electrospun on the first polyurethane nanofiber web to form a laminate in the top-down electrospinning device located at the rear end. At this time, the distance between the nozzle block and the collector was 20 cm and the applied voltage was 15 kV. The basis weight of total nanofiber web was 0.5 g / m2. Thereafter, a cloth fabric having a basis weight of 150 g / m < 2 > was placed on the TPU substrate, and then laminated to produce a bedding nanofiber fabric.
[Example 2]
The polymer spinning solution used for the bottom-up electrospinning device at the front end contains polyurethane to have a concentration of 13%, and the polymer spinning solution used for the top-down electrospinning device at the rear end contains polyvinylidene fluoride The fabric of the bedding nanofiber was prepared in the same manner as in Example 1,
[Example 3]
A bedding nanofiber fabric was prepared in the same manner as in Example 1, except that silver nitrate was contained as an inorganic antibacterial agent, which is an antibacterial substance, in the polymer spinning solution.
[Example 4]
13% by weight of polyurethane (Pellethane 2363-80AE from DOW, USA) was dissolved in 87% by weight of N-dimethylacetamide (DMAc) to prepare a polymer spinning solution having a concentration of 13% Off system designed to inject into each of the spinning liquid main tanks of the bottom-up electrospinning device and the top-down electrospinning device and to separate the nozzle block into two parts in the CD direction and to be connected to the independent main tanks, 15 kV, and electrospun on a TPU substrate (IOH10UM4, manufactured by Bluecher) having a basis weight of 30 g / m < 2 > On the electrospun collector, the basis weight of the polyurethane nanofiber web is 1 g / m 2 in one direction in the CD direction, and the remaining 1 m in one direction is the polyurethane nanosheet having a CD width of 2 m with a basis weight of 0.5 g / A fibrous web was laminated on the TPU substrate, and a cloth weave having a basis weight of 150 g / m < 2 > was placed on the TPU substrate and laminated to produce a bedding nanofiber fabric.
[Example 5]
A bedding nanofiber fabric was prepared in the same manner as in Example 1, except that the electrospinning environment was changed to a temperature of 75 캜 and spinning at a high temperature.
[Example 6]
13% by weight of polyurethane (Pellethane 2363-80AE from DOW, USA) was dissolved in 87% by weight of NN-dimethylacetamide (DMAc) solvent to prepare a polymer spinning solution having a concentration of 13% , And the same polymer spinning solution was provided in the raw material tank of the top-down electrospinning apparatus. Thereafter, a first polyurethane nanofiber web was laminated on a TPU substrate (IOH10UM4 manufactured by Bluecher) having a basis weight of 50 g / m < 2 > in a bottom-up electrospinning apparatus located at the front end, The laminate is rotated 180 degrees. In the top down electrospinning device located at the rear end, the second polyurethane nanofiber web is electrospun on the first polyurethane nanofiber web, and the laminate is rotated 180 degrees through the rotating device. Thereafter, in the bottom-up electrospinning device located at the rear end, the third polyurethane nanofiber web is electrospun on the second polyurethane nanofiber web to form a laminate. At this time, the distance between the nozzle block and the collector was 20 cm and the applied voltage was 15 kV. The basis weight of total nanofiber web was 0.9 g / m2. Thereafter, a cloth fabric having a basis weight of 150 g / m < 2 > was placed on the TPU substrate, and then laminated to produce a bedding nanofiber fabric.
[Comparative Example 1]
After the polyurethane adhesive solution was applied, the bedding fabrics prepared by electrospinning and calendering the nylon 6,6 nanofiber web in a downward direction were used so that a basis weight of the fabric was 150 g / m < 2 > on a basis weight of 0.5 g / .
1) Comparison of production time
The nanofiber webs of Example 1 and Comparative Example 1 were weighed to a basis weight of 0.5 g / m < 2 >, and the time taken for the entire support to wrap around the winding roller was measured and compared.
The bedding-type nanofiber fabric according to the embodiment was found to be free from desorption of nanofibers even though a separate adhesive was not used because the TPU base was used. Also, after 5 times of washing the bedding nanofiber fabric prepared according to Examples 1 to 6, the air permeability efficiencies were all 90% or more, indicating excellent durability. In addition, by using both the bottom-up type and the bottom-up type simultaneously to manufacture the nanofibers, the quality of the nanofiber web, which is an advantage of the bottom-up type, is high and the production efficiency is higher than that of Comparative Example 1 by using the top-down type.
As described above, the method of fabricating the bedding nanofiber fabric according to the present invention is not limited to the configuration and method of the embodiments described above, but the embodiments can be applied to various implementations All or some of the examples may be selectively combined.
1: a nanofiber manufacturing apparatus, 3: a support,
5: feed roller, 7: feed roller,
9: take-up roller, 10: bottom-up electrospinning device,
11: tank main tank, 13: nozzle block,
14: voltage generating device, 15: nozzle,
17: collector, 20: rotating device,
20-1: Flip device,
21, 21 ': left and right guide members,
22, 22 ': left and right guide grooves,
30: top-down electrospinning device, 31: spinning fluid main tank,
33: nozzle block, 35: nozzle
37: collector, 50: laminating device,
60: Temperature control device,
70: air permeability measuring device,
112, 112a, 112b, 112c, 112d, 112e, 112f, 112g, 112h, 112i:
113: Heat line.
Claims (11)
Forming a nanofiber web on the lower surface of the support by electrospinning a polymer spinning solution with a bottom-up electrospinning device; And
And a step of sequentially laminating a nanofiber web by electrospinning the polymer spinning solution with a top-down electrospinning device on the nanofiber web laminated on the support,
The step of electrospinning the polymer spinning solution with the bottom-up electrospinning device to laminate the nanofiber webs and the step of electrospinning the polymer spinning solution with the top-down electrospinning device to laminate the nanofiber webs are alternately performed in two or more stages Respectively,
The step of rotating the lower surface of the supporter through the rotating device by 180 degrees to the upper surface during the step of forming the nanofiber web by the electrospinning device,
Wherein each of the nanofiber webs has a different basis weight on the same plane in the longitudinal direction or in the width direction of the support.
Wherein the total basis weight of each nanofiber web is from 0.1 g / m < 2 > to 20.0 g / m < 2 >.
Wherein the total basis weight of each nanofiber web is from 0.1 g / m < 2 > to less than 1.0 g / m < 2 >.
Wherein the support is one or more selected from the group consisting of a cellulose base, a polyethylene terephthalate base, a bicomponent base, and a thermoplastic polyurethane base.
Wherein each of the polymer spinning solution is the same or different and is characterized in that it is made of polypropylene (PP), polyethylene terephthalate (PET), polyvinylidene fluoride, nylon, polymethylmethacrylate, polyacrylonitrile (PAN) (PUR), polybutylene terephthalate (PBT), polyvinyl butyral, polyvinyl chloride, polyethyleneimine, polylactic acid (PLA), polyvinyl acetate (PVAc), polyethylene naphthalate (PEN), polyvinyl alcohol Characterized in that it is at least one selected from the group consisting of polyvinylidene fluoride (PVA), polyethylene imide (PEI), polycaprolactone (PCL), polylactic glycolic acid (PLGA), and chitosan A method of manufacturing a fabric.
Wherein each polymer spinning solution is one or more selected from the group consisting of polyurethane, polyvinylidene fluoride, and nylon.
Wherein each polymer spinning solution comprises an antibacterial substance.
Further comprising the step of separating the support on which the nanofiber webs are laminated from the support and separately positioning and laminating the support on a substrate after the step of forming the nanofiber webs continuously, A method of manufacturing a textile fabric.
Wherein each of the polymer spinning solution is electrospun through a temperature controller at a temperature of 45 to 120 ° C.
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KR101154212B1 (en) * | 2011-03-20 | 2012-06-18 | 신슈 다이가쿠 | An apparatus for manufacturing separator |
KR101478942B1 (en) * | 2014-01-23 | 2015-01-02 | 해성엔터프라이즈 주식회사 | Method of antibacterial Monofilament and antibacterial Monofilament |
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KR101154212B1 (en) * | 2011-03-20 | 2012-06-18 | 신슈 다이가쿠 | An apparatus for manufacturing separator |
JP2012197526A (en) | 2011-03-20 | 2012-10-18 | Shinshu Univ | Separator manufacturing apparatus |
KR101478942B1 (en) * | 2014-01-23 | 2015-01-02 | 해성엔터프라이즈 주식회사 | Method of antibacterial Monofilament and antibacterial Monofilament |
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