CN112680828A - Preparation method of self-crimping fiber - Google Patents
Preparation method of self-crimping fiber Download PDFInfo
- Publication number
- CN112680828A CN112680828A CN202011469274.7A CN202011469274A CN112680828A CN 112680828 A CN112680828 A CN 112680828A CN 202011469274 A CN202011469274 A CN 202011469274A CN 112680828 A CN112680828 A CN 112680828A
- Authority
- CN
- China
- Prior art keywords
- component
- self
- elasticity
- fiber
- low
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 80
- 238000002788 crimping Methods 0.000 title claims abstract description 27
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 31
- 239000002131 composite material Substances 0.000 claims abstract description 25
- 239000002994 raw material Substances 0.000 claims abstract description 25
- 238000001291 vacuum drying Methods 0.000 claims abstract description 20
- 238000009998 heat setting Methods 0.000 claims abstract description 17
- 238000009987 spinning Methods 0.000 claims abstract description 17
- 230000005540 biological transmission Effects 0.000 claims abstract description 4
- 241000219122 Cucurbita Species 0.000 claims abstract description 3
- 235000009852 Cucurbita pepo Nutrition 0.000 claims abstract description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 30
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 30
- 238000002156 mixing Methods 0.000 claims description 29
- 229920001707 polybutylene terephthalate Polymers 0.000 claims description 27
- 239000004626 polylactic acid Substances 0.000 claims description 27
- 239000002202 Polyethylene glycol Substances 0.000 claims description 24
- 229920000747 poly(lactic acid) Polymers 0.000 claims description 24
- 229920001223 polyethylene glycol Polymers 0.000 claims description 24
- 238000002844 melting Methods 0.000 claims description 23
- 230000008018 melting Effects 0.000 claims description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- -1 polytrimethylene terephthalate Polymers 0.000 claims description 14
- 238000006116 polymerization reaction Methods 0.000 claims description 11
- 239000004814 polyurethane Substances 0.000 claims description 11
- 238000007334 copolymerization reaction Methods 0.000 claims description 10
- 238000011065 in-situ storage Methods 0.000 claims description 10
- 229920002215 polytrimethylene terephthalate Polymers 0.000 claims description 10
- 229920002635 polyurethane Polymers 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- 238000001125 extrusion Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 238000004804 winding Methods 0.000 claims description 7
- 230000004048 modification Effects 0.000 claims description 6
- 238000012986 modification Methods 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 4
- 239000005543 nano-size silicon particle Substances 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 2
- 239000004744 fabric Substances 0.000 abstract description 34
- 239000011148 porous material Substances 0.000 abstract description 23
- 230000008859 change Effects 0.000 abstract description 17
- 230000033228 biological regulation Effects 0.000 abstract description 11
- 230000006870 function Effects 0.000 abstract description 9
- 238000004321 preservation Methods 0.000 abstract description 3
- 230000017525 heat dissipation Effects 0.000 abstract description 2
- 238000001035 drying Methods 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 10
- 230000035945 sensitivity Effects 0.000 description 8
- 230000009975 flexible effect Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000002074 melt spinning Methods 0.000 description 6
- 230000008602 contraction Effects 0.000 description 5
- 239000002657 fibrous material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229910052681 coesite Inorganic materials 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 208000034530 PLAA-associated neurodevelopmental disease Diseases 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000012781 shape memory material Substances 0.000 description 2
- 206010063385 Intellectualisation Diseases 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000002134 carbon nanofiber Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010041 electrostatic spinning Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Abstract
The invention discloses a preparation method of self-crimping fibers, which is characterized in that the self-crimping fibers are of a parallel structure with a cross section in a shape of 8 or gourd, and the self-crimping fibers are prepared by vacuum drying two raw materials, namely a high-elasticity hydrophobic component A and a low-elasticity hydrophilic component B, and carrying out two-component melt preparation, transmission, composite spinning, drafting and heat setting. In the environment with human body surface humidity change, the self-crimping fiber can automatically control the thread pitch through the modulus ratio of dry and wet components in the fiber, adjust the radial stretching behavior of the yarn, further automatically control the pore change in the fabric, finally realize the intelligent regulation and control functions of expanding the pores of the fabric for heat dissipation when the body surface humidity is high and shrinking the pores of the fabric for heat preservation when the body surface humidity is low, and has good wearing comfort.
Description
Technical Field
The invention relates to the field of textile materials, in particular to a preparation method of self-crimping fibers.
Background
In recent years, with the improvement of living conditions, the wearing requirements of people are increasingly improved, and the requirements on the garment fabric tend to be more comfortable and intelligent. However, the current common fiber fabric has low added value, high homogenization degree, low intelligent degree and poor comfort. At present, the modes adopted for realizing the intelligent temperature adjustment of the garment fabric mainly comprise infrared heating regulation and control of the fabric temperature, shape memory fiber regulation of the fabric micropore size and the like. 202010087690.4 discloses a far infrared radiation heating fabric, which has heating function, is uniform, stable, safe and reliable, and can be applied to human body clothes, room temperature heat source, heat preservation and constant temperature material. However, one of the raw materials used by the far infrared radiation heating fabric is a flexible carbon nanofiber membrane, and the preparation process is very complex, expensive, poor in comfort level and difficult to industrially produce. In addition, the intellectualization of the infrared heating fabric is low. 201711450318.X discloses a method for preparing a shape memory fiber membrane with controllable fiber surface micropore structure, the shape memory fiber prepared by electrostatic spinning has uniform micropore structure, and the fiber can have shape memory behavior under environmental stimulation, thereby controlling the micropore size change of the fiber membrane. However, the cost of the fiber is high, the preparation difficulty is high, the fiber only stays in a theoretical level or a small experiment stage, and the shape memory material is often poor in fiber forming performance and difficult to realize large-scale preparation.
Regarding the production method of fiber, the fluffy fabric fiber used in the market at present is prepared by single-component spinning, drafting, twisting, heat setting and untwisting for a long time. When processing in this way, it is usually necessary to generate a permanent crimp profile by physical action of the fiber by external physical action of twisting the fiber by a fiber crimp generating device, but there are problems of long processing flow, high processing cost, and easy abrasion of the fiber. The parallel self-curling fiber precursor can directly obtain a highly-curled three-dimensional spiral structure through simple drafting-heat setting after composite spinning. And the size of the yarn can be effectively adjusted by controlling the spiral angle in the spiral structure, so that a new idea is provided for the development of intelligent fibers. However, the existing self-crimping fibers are all environment-inert materials, and intelligent regulation and control of the yarn length cannot be realized in the change of temperature and humidity in the human body surface environment.
In order to solve the problems faced by the current intelligent garment fabric development, a unique design is carried out by utilizing a fiber self-curling mechanism, and a novel parallel composite fiber which has strong humidity sensitivity and large size and can be used for weaving an intelligent microporous fabric is prepared by taking commercial products such as PTT, PU, PBT, PET, PLA and the like with large quantities and wide range as raw materials through melt spinning. Specifically, a component A with large difference between dry modulus and wet modulus and a component B with no obvious difference between the dry modulus and the wet modulus are designed, and the components are compounded in parallel by taking the cross section as a 8-shaped or gourd-shaped structure. After the two raw materials are subjected to parallel composite spinning by a melting method to prepare protofilaments, the intelligent self-crimping fibers can be prepared by simple drafting and heat setting.
Disclosure of Invention
The invention provides a self-crimping fiber which can adjust the size by self-regulating the change of the body surface humidity of a human body so as to overcome the defects that the existing double-component self-crimping parallel fiber is inert to the environment and the shape memory material is generally poor in fiber forming performance. The self-crimping fiber has the functions of intelligently regulating and controlling the body surface humidity sensitivity: the elastic modulus of the hydrophilic component in the fiber filament is reduced after moisture absorption, the elastic modulus of the hydrophobic component is unchanged, the fiber has a thread pitch difference, and then the length is changed, so that the intelligent regulation and control that the pores of the fabric are expanded to dissipate heat when the body surface humidity is high and the pores of the fabric are contracted to keep warm when the body surface humidity is low are finally realized.
In order to achieve the purpose, the technical scheme of the invention is as follows:
a preparation method of self-crimping fiber, the self-crimping fiber is a parallel structure with a cross section in a shape of 8 or gourd, and is realized by vacuum drying, two-component melt preparation and transmission, composite spinning, drafting and heat setting of two-component raw materials of a high-elasticity hydrophobic component A and a low-elasticity hydrophilic component B;
wherein the high-elasticity hydrophobic component A is prepared from polytrimethylene terephthalate (PTT) [ DuPont China group Co., Ltd.)]Or Polyurethane (PU) [ NatureWorks Corp., USA](ii) a The low-elasticity hydrophilic component B adopts polyethylene glycol (PEG) [ Aladdin Biotech Co., Ltd ]]Or nano-Silica (SiO)2) [ Aladdin Biochemical technology Co Ltd]Modified polylactic acid (PLA) [ NatureWorks Corp., USA ]]Polyethylene glycol (PEG) [ Aladdin Biotech Co Ltd]Or nano-Silica (SiO)2) [ Aladdin Biochemical technology Co Ltd]Modified polyethylene terephthalate (PET) [ BASF ]]Polyethylene glycol (PEG) [ Aladdin Biotech Co Ltd]Or nano-Silica (SiO)2) [ Aladdin Biochemical technology Co Ltd]Modified polybutylene terephthalate (PBT) [ BASF ]]One of (1);
the modification mode of polylactic acid (PLA), polyethylene terephthalate (PET) or polybutylene terephthalate (PBT) by polyethylene glycol (PEG) adopts physical mixing and chemical copolymerization;
the nano silicon dioxide (SiO)2) The modification mode of polylactic acid (PLA) or polyethylene terephthalate (PET) or polybutylene terephthalate (PBT) adopts physical mixing and in-situ polymerization.
The respective preparation and transmission of the two-component melt mean that two raw materials are added into respective screw extruders to be melted and extruded and transmitted in respective screws.
The composite spinning is that two raw materials of a high-elasticity hydrophobic component A and a low-elasticity hydrophilic component B with the mass ratio of (60:40) - (40:60) enter the same spinning box body through respective screws under the extrusion force of the screws, and are extruded by parallel composite spinning components to form parallel primary fibers.
The drafting and heat setting means that the dynamic drafting and tension heat setting of the primary fiber are realized by a drafting roller and a heat setting roller;
the drafting multiplying factor in the drafting process is 1.5-3.5, and the winding speed is 3000-4200 m.min-1。
The invention has the beneficial effects that: the invention adopts two components with different humidity sensitivities, namely a high-elasticity hydrophobic component and a low-elasticity hydrophilic component, which are compounded in parallel, and modifies the hydrophilic component, namely PEG modifies PLA, PET or PBT, or nano SiO by a physical mixing or chemical copolymerization method2The PLA or PET or PBT is modified by physical mixing or in-situ polymerization. In addition, in the environment of human body surface humidity change, the self-crimping fiber can automatically control the thread pitch through the modulus ratio of dry and wet components in the fiber, adjust the radial stretching behavior of the yarn, further automatically control the pore change in the fabric, finally realize the intelligent regulation and control functions of expanding the pores of the fabric for heat dissipation when the body surface humidity is high and shrinking the pores of the fabric for heat preservation when the body surface humidity is low, and has good wearing comfort.
Detailed Description
Example 1
In the preparation method of the self-crimping fiber of the embodiment, the used raw materials are as follows: a high-elastic hydrophobic component A; a low-elasticity hydrophilic component B.
The production process of this example is as follows: slicing the component A, vacuum drying for 8 hours, adding the slices into a screw extruder A for melting and plasticizing, slicing the component B, vacuum drying for 8 hours, adding the slices into a screw extruder B for melting and plasticizing, mixing the raw materials in the screw extruder A and the screw extruder B under the control of a metering pump, performing melt spinning, and performing traction, stretching and heat treatment on the obtained primary fiber to obtain the bi-component composite self-crimping fiber material.
In this example, a high elastic hydrophobic component PTT and a low elastic hydrophilic component PEG modified PET are selected, (physical mixing, i.e., molten PET and PEG are mixed by simple physical and mechanical mixing to reach a molecular level, so as to realize hydrophilic modification of PET by PEG);
slicing the high-elasticity hydrophobic component PTT, placing the slices in a drying box, carrying out vacuum drying for 8 hours at 165 ℃, and then adding the slices into a screw extruder A for melting and plasticizing; and (3) placing the PET slices modified by the low-elasticity hydrophilic component PEG into a drying box, drying for 8 hours in vacuum at the temperature of 165 ℃, and adding into a screw extruder B for melting and plasticizing. Screw extruder A and screw extruder BThe raw materials are as follows: 40, uniformly injecting the mixture into the same composite spinning component, and performing melt extrusion to obtain primary fibers; the raw fiber is subjected to 2 times of high-temperature drafting, tension heat setting and 4100 m-min-1The double-component parallel composite fiber with a spiral structure can be obtained by winding.
In this embodiment, two components with different moisture sensitivities, namely a high-elasticity hydrophobic component and a low-elasticity hydrophilic component, are compounded in parallel, and the hydrophilic component is modified, that is, PEG is used for modifying PLA, PET or PBT, or nano SiO by physical mixing or chemical copolymerization2The PLA or PET or PBT is modified by physical mixing or in-situ polymerization. In addition the self-curling fiber of this embodiment is in people's body surface humidity change environment, and the radial flexible action of yarn is adjusted to the modulus ratio of dry wet component in the accessible fibre than the self-control pitch, and then the pore change in the self-control fabric, and the intelligent regulation and control function that fabric pore expansion dispels the heat when finally realizing body surface humidity is high, fabric pore contraction carries out cold-proof when body surface humidity is low to have good snugness of fit.
Example 2
In the preparation method of the self-crimping fiber of the embodiment, the used raw materials are as follows: a high-elastic hydrophobic component A; a low-elasticity hydrophilic component B.
The production process of this example is as follows: slicing the component A, vacuum drying for 8 hours, adding the slices into a screw extruder A for melting and plasticizing, slicing the component B, vacuum drying for 8 hours, adding the slices into a screw extruder B for melting and plasticizing, mixing the raw materials in the screw extruder A and the screw extruder B under the control of a metering pump, performing melt spinning, and performing traction, stretching and heat treatment on the obtained primary fiber to obtain the bi-component composite self-crimping fiber material.
In the embodiment, the high elastic hydrophobic component PTT and the low elastic hydrophilic component nanometer SiO are selected2Modified PET (in-situ polymerization, namely adding nano silicon dioxide after melting the PET, and polymerizing at a certain temperature to obtain hydrophilic low-elasticity-component PET);
cutting the high-elastic hydrophobic component PTT into slices, placing the slices in a drying box, drying the slices in vacuum at 170 ℃ for 8 hours, and adding the slices into a screw extruder A for melting and plasticizing(ii) a Preparing low-elasticity hydrophilic component nano SiO2And placing the modified PET slices in a drying box, drying for 8 hours in vacuum at 163 ℃, and adding into a screw extruder B for melting and plasticizing. Mixing the raw materials in the screw extruder A and the screw extruder B according to the weight ratio of 50: 50, uniformly injecting the mixture into the same composite spinning component, and performing melt extrusion to obtain primary fibers; the raw fiber is subjected to 1.5 times of drafting, tension heat setting, 4200 m.min-1The double-component parallel composite fiber with a spiral structure can be obtained by winding.
In this embodiment, two components with different moisture sensitivities, namely a high-elasticity hydrophobic component and a low-elasticity hydrophilic component, are compounded in parallel, and the hydrophilic component is modified, that is, PEG is used for modifying PLA, PET or PBT, or nano SiO by physical mixing or chemical copolymerization2The PLA or PET or PBT is modified by physical mixing or in-situ polymerization. In addition the self-curling fiber of this embodiment is in people's body surface humidity change environment, and the radial flexible action of yarn is adjusted to the modulus ratio of dry wet component in the accessible fibre than the self-control pitch, and then the pore change in the self-control fabric, and the intelligent regulation and control function that fabric pore expansion dispels the heat when finally realizing body surface humidity is high, fabric pore contraction carries out cold-proof when body surface humidity is low to have good snugness of fit.
Example 3
In the preparation method of the self-crimping fiber of the embodiment, the used raw materials are as follows: a high-elastic hydrophobic component A; a low-elasticity hydrophilic component B.
The production process of this example is as follows: slicing the component A, vacuum drying for 8 hours, adding the slices into a screw extruder A for melting and plasticizing, slicing the component B, vacuum drying for 8 hours, adding the slices into a screw extruder B for melting and plasticizing, mixing the raw materials in the screw extruder A and the screw extruder B under the control of a metering pump, performing melt spinning, and performing traction, stretching and heat treatment on the obtained primary fiber to obtain the bi-component composite self-crimping fiber material.
In the embodiment, the high elastic hydrophobic component PTT and the low elastic hydrophilic component nanometer SiO are selected2Modified PBT (in-situ polymerization, namely adding nano silicon dioxide after the PBT is melted, keeping a certain temperature for polymerization,thus obtaining the hydrophilic PBT with low elastic component);
slicing the high-elasticity hydrophobic component PTT, placing the slices in a drying box, carrying out vacuum drying at 160 ℃ for 8 hours, and adding the slices into a screw extruder A for melting and plasticizing; preparing low-elasticity hydrophilic component nano SiO2And placing the modified PBT slices in a drying box, carrying out vacuum drying at the temperature of 120 ℃ for 8 hours, and adding the PBT slices into a screw extruder B for melting and plasticizing. Mixing the raw materials in the screw extruder A and the screw extruder B according to the ratio of 55: 45, uniformly injecting the mixture into the same composite spinning assembly, and performing melt extrusion to obtain primary fibers; 2.6 times drafting, tension heat setting, 3500 m.min for raw fiber-1The double-component parallel composite fiber with a spiral structure can be obtained by winding.
In this embodiment, two components with different moisture sensitivities, namely a high-elasticity hydrophobic component and a low-elasticity hydrophilic component, are compounded in parallel, and the hydrophilic component is modified, that is, PEG is used for modifying PLA, PET or PBT, or nano SiO by physical mixing or chemical copolymerization2The PLA or PET or PBT is modified by physical mixing or in-situ polymerization. In addition the self-curling fiber of this embodiment is in people's body surface humidity change environment, and the radial flexible action of yarn is adjusted to the modulus ratio of dry wet component in the accessible fibre than the self-control pitch, and then the pore change in the self-control fabric, and the intelligent regulation and control function that fabric pore expansion dispels the heat when finally realizing body surface humidity is high, fabric pore contraction carries out cold-proof when body surface humidity is low to have good snugness of fit.
Example 4
In the preparation method of the self-crimping fiber of the embodiment, the used raw materials are as follows: a high-elastic hydrophobic component A; a low-elasticity hydrophilic component B.
The production process of this example is as follows: slicing the component A, vacuum drying for 8 hours, adding the slices into a screw extruder A for melting and plasticizing, slicing the component B, vacuum drying for 8 hours, adding the slices into a screw extruder B for melting and plasticizing, mixing the raw materials in the screw extruder A and the screw extruder B under the control of a metering pump, performing melt spinning, and performing traction, stretching and heat treatment on the obtained primary fiber to obtain the bi-component composite self-crimping fiber material.
In this example, the high elastic hydrophobic component PU and the low elastic hydrophilic component nano SiO were selected2Modified PLA (physical mixing, i.e., molten PLA and Nano SiO)2Through simple physical and mechanical mixing, hydrophilic modification of PLA by PEG is realized);
slicing the high-elasticity hydrophobic component PU, placing the sliced high-elasticity hydrophobic component PU in a drying box, carrying out vacuum drying for 8 hours at the temperature of 100 ℃, and then adding the PU into a screw extruder A for melting and plasticizing; preparing low-elasticity hydrophilic component nano SiO2And placing the modified PLA slices in a drying box, performing vacuum drying at the temperature of 120 ℃ for 8 hours, and adding the PLA slices into a screw extruder B for melting and plasticizing. Mixing the raw materials in the screw extruder A and the screw extruder B according to a ratio of 48: 52, uniformly injecting the mixture into the same composite spinning component, and performing melt extrusion to obtain primary fibers; 2.3 times drafting, tension heat setting, 3000 m.min for the original fiber-1The double-component parallel composite fiber with a spiral structure can be obtained by winding.
In this embodiment, two components with different moisture sensitivities, namely a high-elasticity hydrophobic component and a low-elasticity hydrophilic component, are compounded in parallel, and the hydrophilic component is modified, that is, PEG is used for modifying PLA, PET or PBT, or nano SiO by physical mixing or chemical copolymerization2The PLA or PET or PBT is modified by physical mixing or in-situ polymerization. In addition the self-curling fiber of this embodiment is in people's body surface humidity change environment, and the radial flexible action of yarn is adjusted to the modulus ratio of dry wet component in the accessible fibre than the self-control pitch, and then the pore change in the self-control fabric, and the intelligent regulation and control function that fabric pore expansion dispels the heat when finally realizing body surface humidity is high, fabric pore contraction carries out cold-proof when body surface humidity is low to have good snugness of fit.
Example 5
In the preparation method of the self-crimping fiber of the embodiment, the used raw materials are as follows: a high-elastic hydrophobic component A; a low-elasticity hydrophilic component B.
The production process of this example is as follows: slicing the component A, vacuum drying for 8 hours, adding the slices into a screw extruder A for melting and plasticizing, slicing the component B, vacuum drying for 8 hours, adding the slices into a screw extruder B for melting and plasticizing, mixing the raw materials in the screw extruder A and the screw extruder B under the control of a metering pump, performing melt spinning, and performing traction, stretching and heat treatment on the obtained primary fiber to obtain the bi-component composite self-crimping fiber material.
In this example, a high-elasticity hydrophobic component PU and a low-elasticity hydrophilic component PEG-modified PLA (chemical copolymerization, i.e., a copolymerization reaction of a lactic acid monomer and a glycol monomer is performed to obtain a hydrophilic low-elasticity component PLA) are selected;
slicing the high-elasticity hydrophobic component PU, placing the sliced high-elasticity hydrophobic component PU in a drying box, carrying out vacuum drying for 8 hours at the temperature of 100 ℃, and then adding the PU into a screw extruder A for melting and plasticizing; slicing the low-elasticity hydrophilic component PEG modified PLA, placing the sliced PLA in a drying box, carrying out vacuum drying at the temperature of 120 ℃ for 8 hours, and adding the dried PLA into a screw extruder B for melting and plasticizing. Mixing the raw materials in the screw extruder A and the screw extruder B according to a ratio of 40:60, uniformly injecting the mixture into the same composite spinning component, and performing melt extrusion to obtain primary fibers; the raw fiber is subjected to 3 times of drafting, tension heat setting and 3600 m.min-1The double-component parallel composite fiber with a spiral structure can be obtained by winding.
In this embodiment, two components with different moisture sensitivities, namely a high-elasticity hydrophobic component and a low-elasticity hydrophilic component, are compounded in parallel, and the hydrophilic component is modified, that is, PEG is used for modifying PLA, PET or PBT, or nano SiO by physical mixing or chemical copolymerization2The PLA or PET or PBT is modified by physical mixing or in-situ polymerization. In addition the self-curling fiber of this embodiment is in people's body surface humidity change environment, and the radial flexible action of yarn is adjusted to the modulus ratio of dry wet component in the accessible fibre than the self-control pitch, and then the pore change in the self-control fabric, and the intelligent regulation and control function that fabric pore expansion dispels the heat when finally realizing body surface humidity is high, fabric pore contraction carries out cold-proof when body surface humidity is low to have good snugness of fit.
Claims (4)
1. A preparation method of self-crimping fiber is characterized in that the self-crimping fiber is of a parallel structure with a cross section in a shape of 8 or gourd, and is realized by vacuum drying, preparation and transmission of a two-component melt respectively, composite spinning, drafting and heat setting of two-component raw materials of a high-elasticity hydrophobic component A and a low-elasticity hydrophilic component B;
wherein the high-elasticity hydrophobic component A adopts polytrimethylene terephthalate or polyurethane; the low-elasticity hydrophilic component B is one of polyethylene glycol or nano-silica modified polylactic acid, polyethylene glycol or nano-silica modified polyethylene terephthalate, polyethylene glycol or nano-silica modified polybutylene terephthalate;
the modification mode of the polyethylene glycol to polylactic acid or polyethylene terephthalate or polybutylene terephthalate adopts physical mixing or chemical copolymerization;
the modification mode of the nano silicon dioxide to polylactic acid or polyethylene terephthalate or polybutylene terephthalate adopts physical mixing or in-situ polymerization.
2. The method of claim 1, wherein the separate preparation and transportation of the bicomponent melt means that the two materials are fed into separate screw extruders for melting and extrusion transportation in separate screws.
3. The method of claim 1, wherein the composite spinning is carried out by feeding two raw materials, i.e. the high-elasticity hydrophobic component A and the low-elasticity hydrophilic component B, into the same spinning manifold by respective screws under the extrusion force of the screws, and extruding the two raw materials through a parallel composite spinning assembly to form the parallel type proto-fibers.
4. The method for preparing self-curling fiber according to claim 1, wherein the drawing and heat setting are dynamic drawing and tension heat setting of the primary fiber by drawing rollers and heat setting rollers;
the drafting multiplying factor in the drafting process is 1.5-3.5, and the winding speed is 3000-4200 m.min-1。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011469274.7A CN112680828A (en) | 2020-12-14 | 2020-12-14 | Preparation method of self-crimping fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011469274.7A CN112680828A (en) | 2020-12-14 | 2020-12-14 | Preparation method of self-crimping fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
CN112680828A true CN112680828A (en) | 2021-04-20 |
Family
ID=75449472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202011469274.7A Pending CN112680828A (en) | 2020-12-14 | 2020-12-14 | Preparation method of self-crimping fiber |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112680828A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101215723A (en) * | 2008-01-11 | 2008-07-09 | 东华大学 | 8-shaped PET/PTT hollow fibre and preparing method thereof |
CN106149071A (en) * | 2016-08-31 | 2016-11-23 | 王家铭 | Outside bicomponent dies, compound parallel type is from Curl chopped fiber production method |
CN110565184A (en) * | 2019-08-27 | 2019-12-13 | 桐昆集团股份有限公司 | Preparation method of high-self-crimpability PET/PTT parallel composite filament |
CN111206300A (en) * | 2018-11-22 | 2020-05-29 | 厦门翔鹭化纤股份有限公司 | Elastic composite fiber and preparation method thereof |
-
2020
- 2020-12-14 CN CN202011469274.7A patent/CN112680828A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101215723A (en) * | 2008-01-11 | 2008-07-09 | 东华大学 | 8-shaped PET/PTT hollow fibre and preparing method thereof |
CN106149071A (en) * | 2016-08-31 | 2016-11-23 | 王家铭 | Outside bicomponent dies, compound parallel type is from Curl chopped fiber production method |
CN111206300A (en) * | 2018-11-22 | 2020-05-29 | 厦门翔鹭化纤股份有限公司 | Elastic composite fiber and preparation method thereof |
CN110565184A (en) * | 2019-08-27 | 2019-12-13 | 桐昆集团股份有限公司 | Preparation method of high-self-crimpability PET/PTT parallel composite filament |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111455483A (en) | Radiation refrigeration fiber and preparation method of fabric thereof | |
CN110258021B (en) | High-waterproof high-air-permeability nanofiber membrane and preparation method thereof | |
CN103388193A (en) | Preparation method of aerogel modified synthetic fiber and synthetic fiber prepared by same | |
CN104818543A (en) | Modified polylactic acid fiber excellent in performance | |
CN111020777B (en) | Heat-moisture comfortable double-ply yarn and preparation method thereof | |
CN103882547B (en) | A kind of flat acrylic fiber and production method thereof | |
CN111560663A (en) | Preparation method of cross-shaped skin-core moisture absorption and moisture removal fiber | |
CN113774501B (en) | Device for preparing sheath-core fiber based on microfluid coating technology and use method thereof | |
CN109706546B (en) | Graphene sea-island fiber and manufacturing method thereof | |
CN108385231A (en) | Cotton is set with the makeup of sub-micron fibers complex yarn wet guiding function and its application method | |
CN110714236A (en) | Preparation method of moisture-absorbing sweat-releasing antibacterial polyester filament yarn | |
KR20170014063A (en) | Twisted Composite Yarn Based Nanofibers and Method for Manufacturing the Same | |
CN109234820B (en) | Preparation method of polylactic acid short fibers | |
CN109023564B (en) | Preparation method of polylactic acid colored short fibers | |
CN113174647A (en) | Process for producing colored polyester cotton-like special yarn | |
CN112708947A (en) | Preparation method of self-crimping fiber with recycled polyester as raw material | |
CN114059191A (en) | Biodegradable antibacterial fiber and preparation method thereof | |
CN114351279A (en) | Preparation method of aerogel-containing special-shaped polyester staple fibers | |
CN115627559A (en) | Degradable filament and special material thereof | |
CN101165231A (en) | Thin denier flat polyester filament and producing method thereof | |
CN109706545B (en) | Microporous hollow graphene sea-island fiber and manufacturing method thereof | |
KR20170103281A (en) | Method for producing the 4-hole hollow-fiber used R-PET | |
CN112680828A (en) | Preparation method of self-crimping fiber | |
CN104674358B (en) | Specially-shaped spinneret plate | |
CN110804794A (en) | Bi-component heat-humidity comfortable fabric based on hollow polyester fibers and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20210420 |