CN106350932B - Flocking lace fabric - Google Patents
Flocking lace fabric Download PDFInfo
- Publication number
- CN106350932B CN106350932B CN201610708959.XA CN201610708959A CN106350932B CN 106350932 B CN106350932 B CN 106350932B CN 201610708959 A CN201610708959 A CN 201610708959A CN 106350932 B CN106350932 B CN 106350932B
- Authority
- CN
- China
- Prior art keywords
- health care
- layer
- antibiotic health
- flocking
- nylon
- 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.)
- Active
Links
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04B—KNITTING
- D04B21/00—Warp knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
- D04B21/14—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes
- D04B21/16—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes incorporating synthetic threads
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/08—Melt spinning methods
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/08—Melt spinning methods
- D01D5/088—Cooling filaments, threads or the like, leaving the spinnerettes
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/12—Stretch-spinning methods
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D7/00—Collecting the newly-spun products
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D01F1/103—Agents inhibiting growth of microorganisms
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D01F1/106—Radiation shielding agents, e.g. absorbing, reflecting agents
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/90—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyamides
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/04—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of halogenated hydrocarbons
- D10B2321/042—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of halogenated hydrocarbons polymers of fluorinated hydrocarbons, e.g. polytetrafluoroethene [PTFE]
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/06—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of unsaturated alcohols, e.g. polyvinyl alcohol, or of their acetals or ketals
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/02—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Knitting Of Fabric (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention relates to a flocking lace fabric which comprises from the top to the bottom a flocking layer, an antimicrobial acarus prevention layer, a waterproof layer and a support payer. The raw material for the flocking layer is the antimicrobial health care nylon fiber, the fabric for the antimicrobial acarus prevention layer is antimicrobial acarus prevention nylon fiber, the fabric for the waterproof layer is Polytetrafluoroethylene fiber, the fabric for the support layer is polyvinyl alcohol fiber; the antimicrobial health care nylon fiber of the flocking layer and the antimicrobial acarus prevention nylon fiber of the antimicrobial acarus prevention layer are interlocking each other, the antimicrobial acarus prevention nylon fiber of the antimicrobial acarus prevention layer and the Polytetrafluoroethylene fiber of the waterproof layer are interlocking each other. The use of three dimensional warp processing provides the fabric with fabric structure, retains and enhances the strength of the flocking lace fabric to the maximum, possesses good lodging resistance, flame retardant, antimicrobial and waterproof effects; the fabric has broad application potential in the field of warp knitting fabric.
Description
【Technical field】
The present invention relates to lace fabric technical field, is a kind of flocking roses and lace fabric specifically.
【Background technology】
With cloth as base fabric, upper nylon fine hair or viscose glue fine hair are planted in front to flocked fabric, then through steaming and washing processing
Form, matte is plentiful, soft touch, bright color, novel in style, wins the favor of consumer.Flocked fabric is due to hair
The effect of floss, therefore with the warming of certain lint, elasticity, soft effect, nylon fiber is used as the main of flocked fabric
Composition, because nylon fiber has amide structure, has similar structure, nylon fiber and human body skin with the aminoacid of human body
Skin have due to contact parent's clothes sense, therefore in the meaningful advantage of lint application, while nylon fiber itself is with excellent
Elasticity, therefore there is excellent elasticity and skin-friendly on flocked fabric as lint matrix using nylon.
Chinese Patent Application No. 2014106991756 is related to the method for the flocking on uneven, dilute close uneven fabric,
Including：Shorn wool → fine hair dyeing → fine hair electricity process → binding agent prepare → binding agent painting is carried out to base fabric by flocking plate-making
→ electrostatic spinning is covered, feature is first to carry out parent to base fabric before binding agent coating is carried out to uneven, dilute close uneven base fabric
Oiliness process, while in electrostatic spinning, the voltage for controlling flocking machine is 100～120kV；Advantage be due to it is concavo-convex not
Flat, dilute close uneven base fabric carries out first carrying out lipophile process to base fabric before binding agent coating, and in electrostatic spinning, fine hair can
Equably anchored on base fabric by binding agent so that the whole structure after flocking is clean uniform clean and tidy, while in electrostatic spinning,
Using specific voltage so that the cashmere density and fastness after flocking on base fabric all reaches most preferably, improves flocking lace fabric
Deng the class of product.
Chinese Patent Application No. 2011101504774 is related to a kind of spiral-flower flocked lace fabric, belongs to field of textile.
It includes fabric body (1), and in the upper surface of the fabric body (1) disc floret layer (2) is provided with, and disc floret layer (2) surface recombination has
Lace layer (4), in the lower surface of the fabric body (1) cashmere-planted layer (3), the lace layer (4), disc floret layer (2), flocking are provided with
Layer (3) and fabric body (1) are connected as an entirety, and the disc floret layer (2) is provided with disc floret, and the cashmere-planted layer (3) is provided with floss
Spend, the disc floret and velvet flowers are symmetrical.Raised disc floret and velvet flowers enhances the stereovision of spiral-flower flocked lace fabric, and
It is soft comfortable.The hollow out effect of lace brings visual change, dim sensation for fabric.
【The content of the invention】
It is an object of the invention to overcome the deficiencies in the prior art, there is provided a kind of flocking roses and lace fabric.
The purpose of the present invention is achieved through the following technical solutions：
A kind of flocking roses and lace fabric, it is divided into four-layer structure, is followed successively by cashmere-planted layer from top to bottom, antibiosis anti-acarien layer,
Waterproof layer and supporting layer；The raw material of cashmere-planted layer is antibiotic health care nylon fiber, and the raw material of antibiosis anti-acarien layer is antibiosis anti-acarien nylon
Fiber, the raw material of waterproof layer is polytetrafluoroethylene fibre, and the raw material of supporting layer is vinal；The antibiotic health care of cashmere-planted layer
Nylon fiber interweaves with the antibiosis anti-acarien nylon fiber warp knit in antibiosis anti-acarien layer and is connected, the antibiosis anti-acarien Buddhist nun in antibiosis anti-acarien layer
Imperial fiber interweaves with the polytetrafluoroethylene fibre warp knit in waterproof layer and is connected, the polytetrafluoroethylene fibre and supporting layer in waterproof layer
In vinal warp knit interweave connection.
The thickness of described cashmere-planted layer is 300～600 microns.
The thickness of described antibiosis anti-acarien layer is 200～300 microns.
The thickness of described waterproof layer is 200～300 microns.
The thickness of described supporting layer is 200～300 microns.
The grammes per square metre of described flocking roses and lace fabric is 300～800g/m2。
The bursting strength of described flocking roses and lace fabric is 1500～5000N.
Described antibiosis anti-acarien nylon fiber is that by mite-proof agent, antibacterial and nylon chips Jing melt spinning are prepared into
Arrive, be conventional Technology.
Described flocking roses and lace fabric is with antibiotic health care nylon fiber, antibiosis anti-acarien nylon fiber, politef
Fiber, vinal prepares flocking roses and lace fabric using Three-dimensional warp knitting technique.
The flocking roses and lace fabric that multiple structure is arranged, and vinal is used as Rotating fields are supported, to ground,
Glass and plank have it is excellent grab with joint efforts, therefore prevent the skidding of fabric；Simultaneously with waterproof and fire resistance poly- four
Fluorothene is waterproof layer material, using the water proof and anti-flammability of politef, enables flocking roses and lace fabric to intercept water
Infiltration；And antibacterial piles the nylon fiber of layer, in the similar fabric of Three-dimensional warp knitting, flocking roses and lace fabric is imparted excellent
Different antibacterial and the function of anti-mite, while with the thickening nylon with high viscosity and high intensity as raw material in cashmere-planted layer, system
Getting everything ready has the nylon fiber of antibiotic health care and high intensity, imparts the excellent lodging resistance of cashmere-planted layer, uvioresistant performance and antibacterial
Effect；
The preparation method of described antibiotic health care nylon fiber, it is concretely comprised the following steps：
The preparation of first step antibiotic health care nylon master batch
It is 0.25～0.35MPa in pressure with concentrated sulphuric acid as catalyst with trimesic acid and methanol as raw material, reacts
Temperature obtains esterification products trimesic acid under the conditions of 105～120 DEG C, to carry out esterification after 2.5～3.5h of esterification
Methyl ester, after esterification terminates, esterification products go out unreacted methanol in 100 DEG C of vacuum distillations, then add tribromo new penta
Alcohol, then at ambient pressure, carries out ester exchange reaction under the conditions of 125～135 DEG C of reaction temperature, and the ester exchange reaction time is 1.5～
2.5h, prepares solid-phase tack producing modifying agent, then using the method for solid-phase tack producing, with low viscosity nylon chips as raw material, leads to
High temperature thickening is crossed, fine vacuum technics of enhancing viscosity prepares antibiotic health care nylon master batch；
Described trimesic acid is 1 with the molar ratio of methanol:3.5～1:4.5.
The mass concentration of described catalyst concentrated sulphuric acid is 98%, and described catalyst mass fraction in the feed is
1.5～2.5%.
Described trimesic acid is 1 with the molar ratio of tribromoneoamyl alcohol:0.95～1:1.05.
Mass fraction of the described solid-phase tack producing modifying agent in function nylon chips is 10～20%.
The intrinsic viscosity of described low viscosity nylon chips is 1.6～1.8dL/g.
Described solid-phase tack producing process high temperature technics of enhancing viscosity is nitrogen protection normal pressure thickening process, and its high temperature viscosifies temperature
For 210～220 DEG C, the high temperature thickening time is 8～10h, content of carboxyl end group control in section during high temperature thickening for 35～
50mmol/g；
It is 300～60Pa to control vacuum during thickening during described fine vacuum thickening, and fine vacuum viscosifies temperature
For 160～180 DEG C, the fine vacuum thickening time is 8～12h, and it is 15 that content of carboxyl end group in section is controlled during fine vacuum thickening
～25mmol/g；
Described antibiotic health care nylon fiber has antibacterial and far-infrared transmitting function, while with high-viscosity nylon to cut
Piece, prepares and has high intensity, and the nylon of lodging resistance is warp knit fibrous raw material, therefore with excellent mechanical performance.
Used as thermoplastic polymer, it releases in combustion substantial amounts of heat, and the combustion heat is long-range for nylon behavior
In its melting heat, the heat for producing in combustion causes substantial amounts of molten drop, and molten drop does not only result in flame to be continued to spread and pass
Broadcast, while the tissue also to contacting human body causes wound, current nylon fiber flame-retardant system, mainly around the fire-retardant of phosphorus system
Agent, and the blending addition for realizing phosphorus flame retardant in the method being blended, first phosphorus flame retardant is in blend melt spinning process
In, due to the precipitation of phosphorus flame retardant, the spinning and dyeing of nylon are affected, cause lousiness excessive, dyeing quality is poor, and phosphorus system
It mainly accelerates molten drop to fire retardant, takes away heat and flame, it is to avoid nylon burns away the flame retardant effect for playing；Therefore can not
What is avoided causes the expansion of molten drop, and brominated flame-retardant has excellent radical-scavenging ability, using brominated flame-retardant itself
The hydrogen bromide that can carry out radical-scavenging is formed after burning, fire retardant material is then formed, its fire resistance is further lifted,
Improve into carbon；The present invention adopts trimesic acid for raw material, is reacted using methanol and carboxylic esterification, so as to purify equal benzene front three
Acid, it is to avoid due to the high reaction activity of trimesic acid itself, while the more low reason of purity, it is difficult to directly and tribromoneoamyl alcohol
Reaction, causes its further esterification, and reduces the structure of functional groups of itself, it is difficult to carry out ester exchange with later stage esterification products anti-
Should；The trimesic acid methyl ester of methoxy group is prepared by methanol, using trimesic acid methyl ester and tribromoneoamyl alcohol
Ester exchange reaction is carried out, the flame retardant mechanism containing radical-scavenging function is prepared, it is brominated in its flame retardant molecule structure
Measure as 45.14%, benzene ring structure further improves it into carbon in flame retardant molecule, flame retardant effect is improved, using brominated official
Can group and the synergistic effect of benzene ring structure, lifted fire-retardant and into carbon effect, further strengthen thawing resistance energy；Contain in molecule simultaneously
The methoxy functional group of ester exchange reaction can be carried out, methanol is small molecule in Exchange Ester Process, and its boiling point is less than hydrone, and waves
The property sent out is good, and saturated vapour pressure is far below vapour molecule, therefore the methanol that ester exchange is formed beneficial to the de- of polycondensation process small molecular
Remove, especially later stage segment increases, during viscosity increases, small molecule removing is difficult, it is difficult to reach segment propagation process；
Prepared solid-phase tack producing modifying agent contains low molecule ester bond structure for end group, and it is under high temperature and fine vacuum
With contain amide, ester bond and carboxyl structure carry out amidatioon, ester exchange reaction and esterification, so as to improve the molecule of nylon
Amount, lifts the degree of polymerization of nylon；
Solid-phase tack producing is the main method of the high polymer for preparing high molecular, by Solid State Tackifing Technique, realizes that nylon is cut
The molecule propagation process of piece, while by using high temperature ester exchange reaction, enabling solid-phase tack producing modifying agent when faster
Between realize ester exchange reaction, so as to be beneficial to the thickening process of nylon, at the same using fine vacuum viscosify process, make carboxylic in nylon molecules
Acid groups carry out amide reaction with amino, so as to improve the molecular weight of nylon, improve the degree of polymerization of nylon, and due to nylon sheet
The caprolactam of body residual would generally affect the molecular weight of polymer, hence with low-temperature high-vacuum technics of enhancing viscosity, with solid phase increasing
Adhered modification agent and caprolactam ring-opening reaction, not only reduce content of monomer, while also improving the degree of polymerization of nylon itself, improve
The intensity of fiber and fabric；
The preparation of second step antibiotic health care nylon chips
The antibiotic health care nylon master batch obtained with the first step as raw material, with four acicular type zinc oxide crystal whisker and carborundum as anti-purple
Outer modifying agent, by the way of twin screw blending, Jing Screw Extrusion pelletizes prepare antibiotic health care nylon chips；
The mean diameter of described four acicular type zinc oxide crystal whisker is 50～80 nanometers, and the mean diameter of carborundum is 60～80
Nanometer；
Mass fraction of the described four acicular type zinc oxide crystal whisker in antibiotic health care nylon chips is 0.5～1.0%；
Mass fraction of the described carborundum in antibiotic health care nylon chips is 0.5～1.0%；
Four acicular type zinc oxide crystal whisker has excellent antibacterial, uvioresistant and far-infrared transmitting function, can absorb far infrared
Line and be transmitted in surrounding, while the needle point structure of four-needle-like zinc oxide itself, with good electrostatic enrichment performance, because
Tricot lace fabric prepared by this has excellent antibacterial uvioresistant and far-infrared transmitting function and anlistatig effect, makees
There is excellent lodging resistance for flocking roses and lace fabric；Simultaneously carborundum sheet is as rigid structural material, in the fibre
With the rigid purpose for improving fiber, therefore the flocking roses and lace fabric prepared by improving has excellent rigidity, is lifted anti-
Lodging intensity；
Simultaneously after solid-phase tack producing, the strength enhancing of nylon, its lodging resistance increases；
The preparation of the 3rd step antibiotic health care nylon fiber
The antibiotic health care nylon chips that prepared with second step and cut into slices as raw material with high visocity nylon, by melting altogether
Blended ratio technique, Jing high pressure extrusion, side-blown air cooling oils, and stretching and winding prepare antibiotic health care nylon fiber；
The intrinsic viscosity of described high visocity nylon section is 2.45～2.65dL/g；
Mass fraction of the described antibiotic health care nylon chips in antibiotic health care nylon fiber is 20～30%；
Described spinning temperature be 245～265 DEG C, spinning pressure be 15～16MPa, cross air blasting pathogenic wind-warm 28～30
DEG C, cross air blasting wind speed is 1.5～2.0m/min；Draw ratio is 2.5～3.5 times, and draft temperature is 120～135 DEG C, winding speed
Spend for 4500～4800m/min；
So that with material based on high-viscosity nylon, prepared modification of nylon intensity is high, and rigidity is good, therefore for carrying
The intensity and lodging resistance for rising flocked fabric has excellent effect.
Compared with prior art, the positive effect of the present invention is：
It adopts the technique of Three-dimensional warp knitting to flocking roses and lace fabric, by arranging supporting layer, so as to glass, timber has
It is excellent to grab that to close the vinal of intensity be raw material, flocking roses and lace fabric grabbing with joint efforts to glass and plank is improved,
Flocking roses and lace fabric is avoided to skid in use；The politef simultaneously with waterproof and anti-flaming function is anti-
Water layer material, using the water proof and anti-flammability of politef, enables flocking roses and lace fabric to intercept the infiltration of water；Simultaneously
With the nylon fiber with antibiosis anti-acarien function as the raw material of antibiosis anti-acarien layer, excellent anti-of flocking roses and lace fabric is imparted
Bacterium and the function of anti-mite, while being protected as antibacterial with the section of the modification of nylon with high-viscosity nylon chips and Jing solid-phase tack producings
Strong nylon raw fiber, it has intensity high, and lodging resistance is good, and has antibacterial, uvioresistant and far infrared transmission by addition
The four acicular type zinc oxide crystal whisker of function and the carborundum of rigid structure are uvioresistant modifying agent, impart excellent anti-fall of cashmere-planted layer
Fu Xing, uvioresistant performance and antibacterial action；And the lace warp knit technique of Three-dimensional warp knitting, with excellent three dimensional fabric knot of tissue
Structure, the reservation of its maximum possible and the intensity of lifting flocking roses and lace fabric, prepared flocking roses and lace fabric has
The excellent effects such as excellent lodging resistance, fire-retardant, antibacterial, waterproof；Before the fields such as tricot lace fabric have a wide range of applications
Scape.
【Description of the drawings】
The structural representation of Fig. 1 flocking roses and lace fabrics；
Fig. 2 is the preparation reaction equation of solid-phase tack producing modifying agent；
Fig. 3 is the hydrogen nuclear magnetic resonance collection of illustrative plates of the application flocking roses and lace fabric trimesic acid methyl ester；
The hydrogen nuclear magnetic resonance collection of illustrative plates of Fig. 4 solid-phase tack producing modifying agent；
The nuclear magnetic resonance of carbon collection of illustrative plates of Fig. 5 solid-phase tack producing modifying agent；
Labelling in accompanying drawing for：Wherein 1 is supporting layer, and 2 is waterproof layer, and 3 is antibiosis anti-acarien layer, and 4 is cashmere-planted layer.
【Specific embodiment】
A kind of specific embodiment of flocking roses and lace fabric of the invention presented below.
Embodiment 1
Refer to accompanying drawing 1, a kind of flocking roses and lace fabric, it is divided into four-layer structure, and cashmere-planted layer is followed successively by from top to bottom
4, antibiosis anti-acarien layer 3, waterproof layer 2 and supporting layer 1；The raw material of cashmere-planted layer be antibiotic health care nylon fiber, the original of antibiosis anti-acarien layer
Expect for antibiosis anti-acarien nylon fiber, the raw material of waterproof layer is polytetrafluoroethylene fibre, and the raw material of supporting layer is vinal；
The antibiotic health care nylon fiber of cashmere-planted layer interweaves with the antibiosis anti-acarien nylon fiber warp knit in antibiosis anti-acarien layer and is connected, antibiosis anti-acarien
Antibiosis anti-acarien nylon fiber in layer interweaves with the polytetrafluoroethylene fibre warp knit in waterproof layer and is connected, the polytetrafluoro in waterproof layer
Vinyl fiber interweaves with the vinal warp knit in supporting layer and is connected.
The thickness of described cashmere-planted layer is 300～micron.
The thickness of described antibiosis anti-acarien layer is 200 microns.
The thickness of described waterproof layer is 200 microns.
The thickness of described supporting layer is 200 microns.
The grammes per square metre of described flocking roses and lace fabric is 300g/m2。
The bursting strength of described flocking roses and lace fabric is 1500N.
Described antibiosis anti-acarien nylon fiber is that by mite-proof agent, antibacterial and nylon chips Jing melt spinning are prepared into
Arrive, be conventional Technology.
Described flocking roses and lace fabric is with antibiotic health care nylon fiber, antibiosis anti-acarien nylon fiber, politef
Fiber, vinal prepares flocking roses and lace fabric using Three-dimensional warp knitting technique.
The preparation method of described antibiotic health care nylon fiber, it is concretely comprised the following steps：
The preparation of first step antibiotic health care nylon master batch
It is 0.25～0.35MPa in pressure with concentrated sulphuric acid as catalyst with trimesic acid and methanol as raw material, reacts
Temperature obtains esterification products trimesic acid under the conditions of 105～120 DEG C, to carry out esterification after 2.5～3.5h of esterification
Methyl ester, after esterification terminates, esterification products go out unreacted methanol in 100 DEG C of vacuum distillations, then add tribromo new penta
Alcohol, then at ambient pressure, carries out ester exchange reaction under the conditions of 125～135 DEG C of reaction temperature, and the ester exchange reaction time is 1.5～
2.5h, prepares solid-phase tack producing modifying agent, then using the method for solid-phase tack producing, with low viscosity nylon chips as raw material, leads to
High temperature thickening is crossed, fine vacuum technics of enhancing viscosity prepares antibiotic health care nylon master batch；Refer to accompanying drawing 2.
Described trimesic acid is 1 with the molar ratio of methanol：3.5.
The mass concentration of described catalyst concentrated sulphuric acid is 98%, and described catalyst mass fraction in the feed is
1.5%.
Described trimesic acid is 1 with the molar ratio of tribromoneoamyl alcohol：0.95.
Mass fraction of the described solid-phase tack producing modifying agent in function nylon chips is 10%.
The intrinsic viscosity of described low viscosity nylon chips is 1.6dL/g.
Described solid-phase tack producing process high temperature technics of enhancing viscosity is nitrogen protection normal pressure thickening process, and its high temperature viscosifies temperature
For 210～220 DEG C, the high temperature thickening time is 8～10h, and it is 35mmol/ that content of carboxyl end group in section is controlled during high temperature thickening
g；
It is 300～60Pa to control vacuum during thickening during described fine vacuum thickening, and fine vacuum viscosifies temperature
For 160～180 DEG C, the fine vacuum thickening time is 8～12h, content of carboxyl end group in section is controlled during fine vacuum thickening and is
15mmol/g；
Wherein Fig. 3 is the hydrogen nuclear magnetic resonance collection of illustrative plates of the application flocking roses and lace fabric trimesic acid methyl ester, utilizes equal
Benzenetricarboxylic acid reacts under the conditions of sulfuric acid catalyst with methanol and is not detected by generation esterification products, therefore resulting compound
There is a characteristic absorption peak of carboxylic acid and alcoholic extract hydroxyl group, and the characteristic absorption peak of hydrogen on phenyl ring is only detected in collection of illustrative plates, and (δ is
8.90ppm) with hydrogen characteristic absorption peak (δ is 3.90ppm) on methoxyl group, therefore react in esterification reaction process, due to alcohol
It is excessive, make the feature carboxylic acid in reaction on trimesic acid participate in esterification completely；
The simultaneously hydrogen nuclear magnetic resonance collection of illustrative plates of Fig. 4 solid-phase tack producing modifying agent, the hydrogen atom in molecule on each group is corresponding
Chemical shift is as shown in Fig. 4 is composed；Wherein produce because trimesic acid and methanol react generation esterification under the conditions of sulfuric acid catalyst
Thing trimesic acid methyl ester carries out ester exchange reaction with tribromoneoamyl alcohol, so that the alcoholic extract hydroxyl group in tribromoneoamyl alcohol is converted to ester
Key, therefore the characteristic peak (δ is 2.05ppm) of the hydroxyl of tribromoneoamyl alcohol itself is not detected by collection of illustrative plates, and only detect
The characteristic absorption peak of methyl functional group in the tribromo neopentyl oxygen group of tribromoneoamyl alcohol itself, and its corresponding chemical shift by
3.45ppm is transferred to 3.17ppm (b '), therefore illustrates that tribromoneoamyl alcohol has carried out ester exchange reaction with trimesic acid methyl ester；
Methoxyl group itself characteristic absorption peak c ' (δ is 3.89ppm), and c ' groups characteristic peak correspondence hydrogen are also detected that in collection of illustrative plates simultaneously
The ratio of atom peak area peak area corresponding with b ' group characteristic peaks is 3：Hydrogen number ratio on 1, therefore corresponding functional group
For 3:1, existing tribromoneoamyl alcohol carries out 1 with trimesic acid methyl ester:The ester exchange reaction of 1 mol ratio；
Fig. 5 is the nuclear magnetic resonance of carbon collection of illustrative plates of prepared solid-phase tack producing modifying agent, and tribromoneoamyl alcohol is also occurred in that in collection of illustrative plates
With the characteristic absorption peak of the flame-proof modifier that trimesic acid methyl ester carries out ester exchange reaction generation, the corresponding chemistry of wherein d and f
Displacement is respectively δ for the feature suction of the methoxy functional group of trimesic acid methyl ester in 68.5ppm and 35.8ppm, and molecule
Receive peak yet suffer from, and it is corresponding chemistry peak value ratio with；The peak value ratio of the quaternary carbon atom in tribromo neopentyl oxygen ester
For 2:1, therefore illustrate that trimesic acid methyl ester has only carried out 1 with tribromoneoamyl alcohol:1 reaction.
The preparation of second step antibiotic health care nylon chips
The antibiotic health care nylon master batch obtained with the first step as raw material, with four acicular type zinc oxide crystal whisker and carborundum as anti-purple
Outer modifying agent, by the way of twin screw blending, Jing Screw Extrusion pelletizes prepare antibiotic health care nylon chips；
The mean diameter of described four acicular type zinc oxide crystal whisker is 50～80 nanometers, and the mean diameter of carborundum is 60～80
Nanometer；
Mass fraction of the described four acicular type zinc oxide crystal whisker in antibiotic health care nylon chips is 0.5%；
Mass fraction of the described carborundum in antibiotic health care nylon chips is 0.5%；
The preparation of the 3rd step antibiotic health care nylon fiber
The antibiotic health care nylon chips that prepared with second step and cut into slices as raw material with high visocity nylon, by melting altogether
Blended ratio technique, Jing high pressure extrusion, side-blown air cooling oils, and stretching and winding prepare antibiotic health care nylon fiber；
The intrinsic viscosity of described high visocity nylon section is 2.45dL/g；
Mass fraction of the described antibiotic health care nylon chips in antibiotic health care nylon fiber is 20%；
Described spinning temperature be 245～265 DEG C, spinning pressure be 15～16MPa, cross air blasting pathogenic wind-warm 28～30
DEG C, cross air blasting wind speed is 1.5～2.0m/min；Draw ratio is 2.5～3.5 times, and draft temperature is 120～135 DEG C, winding speed
Spend for 4500～4800m/min；
Embodiment 2
A kind of flocking roses and lace fabric, it is divided into four-layer structure, is followed successively by cashmere-planted layer from top to bottom, antibiosis anti-acarien layer,
Waterproof layer and supporting layer；The raw material of cashmere-planted layer is antibiotic health care nylon fiber, and the raw material of antibiosis anti-acarien layer is antibiosis anti-acarien nylon
Fiber, the raw material of waterproof layer is polytetrafluoroethylene fibre, and the raw material of supporting layer is vinal；The antibiotic health care of cashmere-planted layer
Nylon fiber interweaves with the antibiosis anti-acarien nylon fiber warp knit in antibiosis anti-acarien layer and is connected, the antibiosis anti-acarien Buddhist nun in antibiosis anti-acarien layer
Imperial fiber interweaves with the polytetrafluoroethylene fibre warp knit in waterproof layer and is connected, the polytetrafluoroethylene fibre and supporting layer in waterproof layer
In vinal warp knit interweave connection.
The thickness of described cashmere-planted layer is 600 microns.
The thickness of described antibiosis anti-acarien layer is 300 microns.
The thickness of described waterproof layer is 300 microns.
The thickness of described supporting layer is 300 microns.
The grammes per square metre of described flocking roses and lace fabric is 800g/m2。
The bursting strength of described flocking roses and lace fabric is 5000N.
Described antibiosis anti-acarien nylon fiber is that by mite-proof agent, antibacterial and nylon chips Jing melt spinning are prepared into
Arrive, be conventional Technology.
Described flocking roses and lace fabric is with antibiotic health care nylon fiber, antibiosis anti-acarien nylon fiber, politef
Fiber, vinal prepares flocking roses and lace fabric using Three-dimensional warp knitting technique.
The preparation method of described antibiotic health care nylon fiber, it is concretely comprised the following steps：
The preparation of first step antibiotic health care nylon master batch
It is 0.25～0.35MPa in pressure with concentrated sulphuric acid as catalyst with trimesic acid and methanol as raw material, reacts
Temperature obtains esterification products trimesic acid under the conditions of 105～120 DEG C, to carry out esterification after 2.5～3.5h of esterification
Methyl ester, after esterification terminates, esterification products go out unreacted methanol in 100 DEG C of vacuum distillations, then add tribromo new penta
Alcohol, then at ambient pressure, carries out ester exchange reaction under the conditions of 125～135 DEG C of reaction temperature, and the ester exchange reaction time is 1.5～
2.5h, prepares solid-phase tack producing modifying agent, then using the method for solid-phase tack producing, with low viscosity nylon chips as raw material, leads to
High temperature thickening is crossed, fine vacuum technics of enhancing viscosity prepares antibiotic health care nylon master batch；
Described trimesic acid is 1 with the molar ratio of methanol：4.5.
The mass concentration of described catalyst concentrated sulphuric acid is 98%, and described catalyst mass fraction in the feed is
2.5%.
Described trimesic acid is 1 with the molar ratio of tribromoneoamyl alcohol：1.05.
Mass fraction of the described solid-phase tack producing modifying agent in function nylon chips is 20%.
The intrinsic viscosity of described low viscosity nylon chips is 1.8dL/g.
Described solid-phase tack producing process high temperature technics of enhancing viscosity is nitrogen protection normal pressure thickening process, and its high temperature viscosifies temperature
For 210～220 DEG C, the high temperature thickening time is 8～10h, and it is 50mmol/ that content of carboxyl end group in section is controlled during high temperature thickening
g；
It is 300～60Pa to control vacuum during thickening during described fine vacuum thickening, and fine vacuum viscosifies temperature
For 160～180 DEG C, the fine vacuum thickening time is 8～12h, content of carboxyl end group in section is controlled during fine vacuum thickening and is
25mmol/g；
The preparation of second step antibiotic health care nylon chips
The antibiotic health care nylon master batch obtained with the first step as raw material, with four acicular type zinc oxide crystal whisker and carborundum as anti-purple
Outer modifying agent, by the way of twin screw blending, Jing Screw Extrusion pelletizes prepare antibiotic health care nylon chips；
The mean diameter of described four acicular type zinc oxide crystal whisker is 50～80 nanometers, and the mean diameter of carborundum is 60～80
Nanometer；
Mass fraction of the described four acicular type zinc oxide crystal whisker in antibiotic health care nylon chips is 1.0%；
Mass fraction of the described carborundum in antibiotic health care nylon chips is 1.0%；
The preparation of the 3rd step antibiotic health care nylon fiber
The antibiotic health care nylon chips that prepared with second step and cut into slices as raw material with high visocity nylon, by melting altogether
Blended ratio technique, Jing high pressure extrusion, side-blown air cooling oils, and stretching and winding prepare antibiotic health care nylon fiber；
The intrinsic viscosity of described high visocity nylon section is 2.65dL/g；
Mass fraction of the described antibiotic health care nylon chips in antibiotic health care nylon fiber is 30%；
Described spinning temperature be 245～265 DEG C, spinning pressure be 15～16MPa, cross air blasting pathogenic wind-warm 28～30
DEG C, cross air blasting wind speed is 1.5～2.0m/min；Draw ratio is 2.5～3.5 times, and draft temperature is 120～135 DEG C, winding speed
Spend for 4500～4800m/min；
Embodiment 3
A kind of flocking roses and lace fabric, it is divided into four-layer structure, is followed successively by cashmere-planted layer from top to bottom, antibiosis anti-acarien layer,
Waterproof layer and supporting layer；The raw material of cashmere-planted layer is antibiotic health care nylon fiber, and the raw material of antibiosis anti-acarien layer is antibiosis anti-acarien nylon
Fiber, the raw material of waterproof layer is polytetrafluoroethylene fibre, and the raw material of supporting layer is vinal；The antibiotic health care of cashmere-planted layer
Nylon fiber interweaves with the antibiosis anti-acarien nylon fiber warp knit in antibiosis anti-acarien layer and is connected, the antibiosis anti-acarien Buddhist nun in antibiosis anti-acarien layer
Imperial fiber interweaves with the polytetrafluoroethylene fibre warp knit in waterproof layer and is connected, the polytetrafluoroethylene fibre and supporting layer in waterproof layer
In vinal warp knit interweave connection.
The thickness of described cashmere-planted layer is 400 microns.
The thickness of described antibiosis anti-acarien layer is 250 microns.
The thickness of described waterproof layer is 250 microns.
The thickness of described supporting layer is 250 microns.
The grammes per square metre of described flocking roses and lace fabric is 600g/m2。
The bursting strength of described flocking roses and lace fabric is 4500N.
Described antibiosis anti-acarien nylon fiber is that by mite-proof agent, antibacterial and nylon chips Jing melt spinning are prepared into
Arrive, be conventional Technology.
Described flocking roses and lace fabric is with antibiotic health care nylon fiber, antibiosis anti-acarien nylon fiber, politef
Fiber, vinal prepares flocking roses and lace fabric using Three-dimensional warp knitting technique.
The preparation method of described antibiotic health care nylon fiber, it is concretely comprised the following steps：
The preparation of first step antibiotic health care nylon master batch
It is 0.25～0.35MPa in pressure with concentrated sulphuric acid as catalyst with trimesic acid and methanol as raw material, reacts
Temperature obtains esterification products trimesic acid under the conditions of 105～120 DEG C, to carry out esterification after 2.5～3.5h of esterification
Methyl ester, after esterification terminates, esterification products go out unreacted methanol in 100 DEG C of vacuum distillations, then add tribromo new penta
Alcohol, then at ambient pressure, carries out ester exchange reaction under the conditions of 125～135 DEG C of reaction temperature, and the ester exchange reaction time is 1.5～
2.5h, prepares solid-phase tack producing modifying agent, then using the method for solid-phase tack producing, with low viscosity nylon chips as raw material, leads to
High temperature thickening is crossed, fine vacuum technics of enhancing viscosity prepares antibiotic health care nylon master batch；
Described trimesic acid is 1 with the molar ratio of methanol：4.0.
The mass concentration of described catalyst concentrated sulphuric acid is 98%, and described catalyst mass fraction in the feed is
2.0%.
Described trimesic acid is 1 with the molar ratio of tribromoneoamyl alcohol：1.
Mass fraction of the described solid-phase tack producing modifying agent in function nylon chips is 15%.
The intrinsic viscosity of described low viscosity nylon chips is 1.75dL/g.
Described solid-phase tack producing process high temperature technics of enhancing viscosity is nitrogen protection normal pressure thickening process, and its high temperature viscosifies temperature
For 210～220 DEG C, the high temperature thickening time is 8～10h, and it is 45mmol/ that content of carboxyl end group in section is controlled during high temperature thickening
g；
It is 300～60Pa to control vacuum during thickening during described fine vacuum thickening, and fine vacuum viscosifies temperature
For 160～180 DEG C, the fine vacuum thickening time is 8～12h, content of carboxyl end group in section is controlled during fine vacuum thickening and is
20mmol/g；
The preparation of second step antibiotic health care nylon chips
The antibiotic health care nylon master batch obtained with the first step as raw material, with four acicular type zinc oxide crystal whisker and carborundum as anti-purple
Outer modifying agent, by the way of twin screw blending, Jing Screw Extrusion pelletizes prepare antibiotic health care nylon chips；
The mean diameter of described four acicular type zinc oxide crystal whisker is 50～80 nanometers, and the mean diameter of carborundum is 60～80
Nanometer；
Mass fraction of the described four acicular type zinc oxide crystal whisker in antibiotic health care nylon chips is 0.75%；
Mass fraction of the described carborundum in antibiotic health care nylon chips is 0.75%；
The preparation of the 3rd step antibiotic health care nylon fiber
The antibiotic health care nylon chips that prepared with second step and cut into slices as raw material with high visocity nylon, by melting altogether
Blended ratio technique, Jing high pressure extrusion, side-blown air cooling oils, and stretching and winding prepare antibiotic health care nylon fiber；
The intrinsic viscosity of described high visocity nylon section is 2.50dL/g；
Mass fraction of the described antibiotic health care nylon chips in antibiotic health care nylon fiber is 25%；
Described spinning temperature be 245～265 DEG C, spinning pressure be 15～16MPa, cross air blasting pathogenic wind-warm 28～30
DEG C, cross air blasting wind speed is 1.5～2.0m/min；Draw ratio is 2.5～3.5 times, and draft temperature is 120～135 DEG C, winding speed
Spend for 4500～4800m/min；
The above is only the preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art
Member, without departing from the inventive concept of the premise, can also make some improvements and modifications, and these improvements and modifications also should be regarded as
In protection scope of the present invention.
Claims (9)
1. a kind of flocking roses and lace fabric, it is characterised in that it is divided into four-layer structure, and cashmere-planted layer is followed successively by from top to bottom, resists
The anti-mite layer of bacterium, waterproof layer and supporting layer；The raw material of cashmere-planted layer is antibiotic health care nylon fiber, and the raw material of antibiosis anti-acarien layer is antibacterial
Anti-mite nylon fiber, the raw material of waterproof layer is polytetrafluoroethylene fibre, and the raw material of supporting layer is vinal；Cashmere-planted layer
Antibiotic health care nylon fiber interweaves with the antibiosis anti-acarien nylon fiber warp knit in antibiosis anti-acarien layer and is connected, anti-in antibiosis anti-acarien layer
The anti-mite nylon fiber of bacterium interweaves with the polytetrafluoroethylene fibre warp knit in waterproof layer and is connected, the polytetrafluoroethylene fibre in waterproof layer
Interweave with the vinal warp knit in supporting layer and be connected；
The preparation method of described antibiotic health care nylon fiber, it is concretely comprised the following steps：
The preparation of first step antibiotic health care nylon master batch
With trimesic acid and methanol as raw material, with concentrated sulphuric acid as catalyst, pressure be 0.25～0.35MPa, reaction temperature
Under the conditions of for 105～120 DEG C, esterification is carried out, esterification products trimesic acid first is obtained after 2.5～3.5h of esterification
Ester, after esterification terminates, esterification products go out unreacted methanol in 100 DEG C of vacuum distillations, then add tribromoneoamyl alcohol,
Then at ambient pressure, ester exchange reaction is carried out under the conditions of 125～135 DEG C of reaction temperature, the ester exchange reaction time is 1.5～
2.5h, prepares solid-phase tack producing modifying agent, then using the method for solid-phase tack producing, with low viscosity nylon chips as raw material, leads to
High temperature thickening is crossed, fine vacuum technics of enhancing viscosity prepares antibiotic health care nylon master batch；
Described solid-phase tack producing process high temperature technics of enhancing viscosity is nitrogen protection normal pressure thickening process, and its high temperature thickening temperature is
210～220 DEG C, the high temperature thickening time is 8～10h, and it is 35～50 that content of carboxyl end group in section is controlled during high temperature thickening
mmol/g；
It is 300～60Pa that vacuum during thickening is controlled during described fine vacuum thickening, and fine vacuum thickening temperature is 160
～180 DEG C, the fine vacuum thickening time is 8～12h, and it is 15～25 that content of carboxyl end group in section is controlled during fine vacuum thickening
mmol/g；
The preparation of second step antibiotic health care nylon chips
The antibiotic health care nylon master batch obtained with the first step is changed with four acicular type zinc oxide crystal whisker and carborundum as raw material as uvioresistant
Property agent, using twin screw blending by the way of, Jing Screw Extrusion pelletizes prepare antibiotic health care nylon chips；
The preparation of the 3rd step antibiotic health care nylon fiber
The antibiotic health care nylon chips that prepared with second step and cut into slices as raw material with high visocity nylon, spun by melt blending
Silk technique, Jing high pressure extrusion, side-blown air cooling oils, and stretching and winding prepare antibiotic health care nylon fiber.
2. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that described flocking roses and lace fabric
Grammes per square metre be 300～800 g/m2。
3. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that described flocking roses and lace fabric
Bursting strength be 1500～5000N.
4. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that in the system of antibiotic health care nylon master batch
In standby, described trimesic acid and the molar ratio of methanol is 1:3.5～1:4.5.
5. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that in the system of antibiotic health care nylon master batch
In standby, described trimesic acid and the molar ratio of tribromoneoamyl alcohol is 1:0.95～1:1.05.
6. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that in the system of antibiotic health care nylon master batch
In standby, the mass fraction of described solid-phase tack producing modifying agent in antibiotic health care nylon master batch is 10～20%.
7. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that in the system of antibiotic health care nylon chips
In standby, the mass fraction of described four acicular type zinc oxide crystal whisker in antibiotic health care nylon chips is 0.5～1.0%.
8. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that in the system of antibiotic health care nylon chips
In standby, the mass fraction of described carborundum in antibiotic health care nylon chips is 0.5～1.0%.
9. a kind of flocking roses and lace fabric as claimed in claim 1, it is characterised in that in the system of antibiotic health care nylon chips
In standby, the mass fraction of described antibiotic health care nylon chips in antibiotic health care nylon fiber is 20～30%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610708959.XA CN106350932B (en) | 2016-08-24 | 2016-08-24 | Flocking lace fabric |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610708959.XA CN106350932B (en) | 2016-08-24 | 2016-08-24 | Flocking lace fabric |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106350932A CN106350932A (en) | 2017-01-25 |
| CN106350932B true CN106350932B (en) | 2017-05-03 |
Family
ID=57844614
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610708959.XA Active CN106350932B (en) | 2016-08-24 | 2016-08-24 | Flocking lace fabric |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106350932B (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107419532A (en) * | 2017-06-19 | 2017-12-01 | 江苏宏圣达花边有限公司 | A kind of handling process of the anti-mite lace fabric of antibacterial |
| CN109111642A (en) * | 2018-06-08 | 2019-01-01 | 苏州西玛家具股份有限公司 | One kind having waterproof anti-corrosion Environment-friendlyplastic plastic flitch |
| CN109480350A (en) * | 2018-12-11 | 2019-03-19 | 广州凯乐石运动用品有限公司 | With a cube wind coat for empty Nest architecture |
| CN110152956A (en) * | 2019-05-31 | 2019-08-23 | 锦州希尔达汽车零部件有限公司 | A kind of production method of the high light shine implanted article of automotive upholstery |
| CN111016347A (en) * | 2019-11-25 | 2020-04-17 | 江苏惟妙纺织科技有限公司 | Anti-ultraviolet colorful color-changing fiber lace |
| CN111850799A (en) * | 2020-06-03 | 2020-10-30 | 福州标顺信息科技有限公司 | Preparation method of antibacterial wear-resistant apocynum venetum fiber lace |
| WO2022146689A1 (en) * | 2020-12-28 | 2022-07-07 | University Of Massachusetts | Antibacterial/viral disinfecting-effective air scrubber/purifier filter material and filters |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3772131A (en) * | 1971-10-01 | 1973-11-13 | Burlington Industries Inc | Flocked spunlaced blanket |
| CN201381410Y (en) * | 2009-02-19 | 2010-01-13 | 江苏浩华纺织有限公司 | Modal fiber dyed fabric |
| CN203792824U (en) * | 2014-04-15 | 2014-08-27 | 福建省百凯经编实业有限公司 | Breathable knitted lace shell fabric with four-layer structure |
| CN203792823U (en) * | 2014-04-15 | 2014-08-27 | 福建省百凯经编实业有限公司 | Anti-microbial glossy shell fabric with knitted lace |
| KR20150086965A (en) * | 2014-01-21 | 2015-07-29 | 정승원 | Method of manufacturing lace cloth |
| CN105015089A (en) * | 2014-04-26 | 2015-11-04 | 孙建良 | Spiral flocking elastic fabric |
| CN205989546U (en) * | 2016-08-24 | 2017-03-01 | 福建省百凯经编实业有限公司 | Flocking roses and lace fabric |
-
2016
- 2016-08-24 CN CN201610708959.XA patent/CN106350932B/en active Active
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3772131A (en) * | 1971-10-01 | 1973-11-13 | Burlington Industries Inc | Flocked spunlaced blanket |
| CN201381410Y (en) * | 2009-02-19 | 2010-01-13 | 江苏浩华纺织有限公司 | Modal fiber dyed fabric |
| KR20150086965A (en) * | 2014-01-21 | 2015-07-29 | 정승원 | Method of manufacturing lace cloth |
| CN203792824U (en) * | 2014-04-15 | 2014-08-27 | 福建省百凯经编实业有限公司 | Breathable knitted lace shell fabric with four-layer structure |
| CN203792823U (en) * | 2014-04-15 | 2014-08-27 | 福建省百凯经编实业有限公司 | Anti-microbial glossy shell fabric with knitted lace |
| CN105015089A (en) * | 2014-04-26 | 2015-11-04 | 孙建良 | Spiral flocking elastic fabric |
| CN205989546U (en) * | 2016-08-24 | 2017-03-01 | 福建省百凯经编实业有限公司 | Flocking roses and lace fabric |
Also Published As
| Publication number | Publication date |
|---|---|
| CN106350932A (en) | 2017-01-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106350932B (en) | Flocking lace fabric | |
| CN107385545B (en) | A kind of preparation method and application of the copolyesteramide and its fiber that graphene oxide is modified | |
| CA3005917C (en) | Modified fiber and preparation method therefor | |
| CN106350894B (en) | Graphene polyester monofilament | |
| CN101792578B (en) | Polyester fiber with functions of wetting, moisture transmitting and quick drying and fabric thereof | |
| CN106367884B (en) | Antibacterial warp-knitted lace fabric and preparation method thereof | |
| CN105839220B (en) | A kind of AABB type Long carbon chain polyetheramide elastomeric fibers and its preparation method and application | |
| CN107502974A (en) | A kind of method that covering yarn of chopped fiber bag micropore alkali soluble polyester long filament prepares hollow woven product | |
| JP2011162907A (en) | Crimped yarn and fibrous structure | |
| CN106498542B (en) | It is a kind of without dye environmental protection flame retardant fiber and preparation method thereof | |
| CN105177748A (en) | Colored flame-retardant flashing profiled polyester filament and preparation method thereof | |
| CN111910285A (en) | Graphene biological composite fiber and preparation method and application thereof | |
| CN108866668A (en) | A kind of nano flame-retardant fiber and preparation method thereof | |
| CN106400175A (en) | Production method of pre-spinning colored high-shrinkage polyester FDYs (Fully Drawn Yarns) | |
| CN106521690A (en) | Microcrystalline cellulose-modified polyester fiber and preparation method thereof | |
| CN104831466B (en) | A kind of manufacture method of the screen cloth for bedding | |
| CN106337249B (en) | Low-elastic-yarn warp-knitted lace fabric | |
| CN103122500B (en) | A kind of Splittable conjugate fiber and obtained Superfine Fibre Fabric thereof | |
| CN106350892B (en) | Anti-flaming tricot lace fabric and production method thereof | |
| CN106319749B (en) | Wool-imitated tricot lace fabric | |
| CN102585187B (en) | Modified copolyester and preparation method as well as application thereof | |
| CN101967757A (en) | Composite nonwoven fabric | |
| CN109321999A (en) | A kind of efficient far infrared, 6 fiber of ultraviolet resistant nylon and preparation method thereof | |
| CN104420073A (en) | Lotus fiber non-woven fabric | |
| CN109837763A (en) | A kind of preparation method of pearl powder base uvioresistant fabric |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |