CN109137127A - It is a kind of with anion, far infrared, healthcare function polyester fiber - Google Patents

It is a kind of with anion, far infrared, healthcare function polyester fiber Download PDF

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Publication number
CN109137127A
CN109137127A CN201810745742.5A CN201810745742A CN109137127A CN 109137127 A CN109137127 A CN 109137127A CN 201810745742 A CN201810745742 A CN 201810745742A CN 109137127 A CN109137127 A CN 109137127A
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Prior art keywords
filler
polyester fiber
nanoparticle
nife
zno
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罗鼎明
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Foshan Nanhai Beauty Underwear Co Ltd
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Foshan Nanhai Beauty Underwear Co Ltd
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Priority to CN201810745742.5A priority Critical patent/CN109137127A/en
Publication of CN109137127A publication Critical patent/CN109137127A/en
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent 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
    • D01F6/92Monocomponent 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 polyesters
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • D01F1/106Radiation shielding agents, e.g. absorbing, reflecting agents

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Artificial Filaments (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

This application involves it is a kind of with anion, far infrared, healthcare function polyester fiber, the polyester fiber is using polyester as substrate, using filler A, filler B, filler C as additive, blended is prepared by melting;The filler A includes: ZrO2Nano-powder and ZnO nanoparticle;The filler B includes: tourmaline nano particle and ZnO nanoparticle;The filler C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.

Description

It is a kind of with anion, far infrared, healthcare function polyester fiber
Technical field
This application involves polyester fiber technical field more particularly to it is a kind of with anion, far infrared, healthcare function it is poly- Ester fiber.
Background technique
Currently, the functionalization exploitation of textile is more and more important with the development of industrialization technology;By in fiber or spinning Addition has the substance of far infrared transmission property in fabric, can absorb the heat that solar energy and human body distribute, and be transmitted back to The far infrared that needed by human body is wanted plays positive warming effect using thermogenetic effect of the far infrared to human body, meanwhile, have Promote blood circulation of human body and metabolism, has the function of eliminating fatigue, regain one's strength;It is born further, it is also possible to add and have The substance of ion function.
In the prior art, usually the powder with anion or far-infrared transmitting function is added in fabric, makes its tool Standby certain anion or far-infrared transmitting function, however, in the prior art, it is common that by adding single substance, in realization Function is stated, the functionality of fabric is more single, and effect is undesirable.
Summary of the invention
The present invention is intended to provide it is a kind of with anion, far infrared, healthcare function polyester fiber, it is set forth above to solve Problem.
Provided in the embodiment of the present invention it is a kind of with anion, far infrared, healthcare function polyester fiber, the polyester Fiber is using polyester as substrate, using filler A, filler B, filler C as additive, by melting blended be prepared;The filler A packet It includes: ZrO2Nano-powder and ZnO nanoparticle;The filler B includes: tourmaline nano particle and ZnO nanoparticle;It is described to fill out Expect that C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.
The technical solution that the embodiment of the present invention provides can include the following benefits:
The invention using zinc oxide nano-particle as the dispersing agent of filler, achieve unexpected technology effect Fruit;Also, in filler C, ZnO nanoparticle and NiFe2O4Nanoparticle synergistic effect, the performance for electro-magnetic screen function Play good effect.
The additional aspect of the application and advantage will be set forth in part in the description, and will partially become from the following description It obtains obviously, or recognized by the practice of the application.It should be understood that above general description and following detailed description are only Be it is exemplary and explanatory, the application can not be limited.
Specific embodiment
Example embodiments are described in detail here, embodiment described in following exemplary embodiment Do not represent all embodiments consistented with the present invention.On the contrary, they be only with as being described in detail in the appended claims , the examples of the device and method that some aspects of the invention are consistent.
Embodiments herein be related to it is a kind of with anion, far infrared, healthcare function polyester fiber, by polyester Nanocomposite is added in fiber, so that polyester functional fibre has anion, far infrared transmission and electro-magnetic screen function.
Specifically, the polyester fiber is using polyester as substrate, it is mixed by melting using filler A, filler B, filler C as additive Spinning is prepared;In terms of content, raw material according to the filler A that weight percent includes: 3~9%, 8~12% filler B, 4 ~10% filler C, surplus are polyester.
Filler A includes: ZrO2Nano-powder and ZnO nanoparticle;Filler B includes: tourmaline nano particle and ZnO Nanoparticle;Filler C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.
In the prior art, have and carry out melting spinning by the way that tourmaline powder, sepiolite, pearl powder to be added in polyester fondant Silk, is made polyester fiber with health care function;However, those skilled in the art understand that, the partial size of usual nano material Smaller, surface-active and free energy are higher, cause the nano particle of addition to have agglomeration tendency, this will largely effect on functionality Particle plays a role;Meanwhile causing polyester fiber modified effect unobvious.
In technical solution of the present invention, using filler A, filler B and filler C as additive, by melt it is blended be prepared it is poly- Ester fiber, by controlling mass ratio, above-mentioned filler A, filler B and filler C synergistic effect, so that the polyester functional fibre has Anion, far infrared transmission, electro-magnetic screen function, have expanded the application range of polyester fiber significantly;In addition, the filler It A, include dispersing agent ZnO nanoparticle in filler B and filler C, which can be effective in polyester fiber preparation process The reunion for preventing additive is conducive to the performance of anion, far infrared, electromagnetic shielding performance, achieves unexpected beneficial Effect.
In a kind of preferred embodiment, above-mentioned ZnO nanoparticle partial size is 20-50nm, preferably 30nm.
Zinc oxide is a kind of important semiconductor material, is widely used in plastics, silicate product, synthetic rubber, profit In the production of the products such as lubricating oil, paint, ointment, adhesive, food, battery, fire retardant.The band gap and exciton of zinc oxide Binding energy is larger, and transparency is high, there is excellent room temperature luminescent properties, the liquid crystal display of semiconductor field, thin film transistor (TFT), There is application in the products such as light emitting diode.It is creative using zinc oxide nano-particle as filler in technical scheme Dispersing agent, unexpected technical results have been achieved;Also, in filler C, ZnO nanoparticle and NiFe2O4Nanoparticle Synergistic effect, plays good effect for the performance of electro-magnetic screen function.
It is related to above-mentioned filler separately below:
Filler A is far infrared additive, wherein the ZrO2Nano-powder is to be prepared by ultrasonic microemulsion liquid method.
Currently, the exploitation about far-infrared material is concentrated mainly on far-infrared ceramic powder, far-infrared ceramic powder master If containing Mn, Fe, Co and its oxide, however, currently, the average particle size of room temperature far-infrared ceramic powder still in micron order, Its far infrared radiation rate is relatively low.ZrO2Powder is production zirconium oxide special cermacis, high grade refractory, optical communication device, new energy The basic material of source material, ZrO2With low-temperature sintering, ZrO2Nano-powder is as a kind of non-toxic and non-radioactive and has low The material of warm far infrared transmission performance is a kind of important far infrared additive;However, if by above-mentioned ZrO2Nano-powder is straight It connects and is added in polyester fiber, due to nanometer reuniting effect, ZrO2Nano-powder disperses unevenly in polyester fiber, can significantly Reduce the performance of far infrared performance;In technical scheme, by by ZrO2Nano-powder and ZnO nanoparticle dispersing agent are mixed It closes, calcining, has obtained filler A, be then added into polyester fiber again.In above-mentioned mixing, calcination process, so that ZrO2It receives Rice flour body can effectively adsorb and be incorporated in ZnO nanoparticle surface, substantially increase the uniformity of far infrared transmission, generate Unexpected technical effect.
Preferably, in filler A, the mass fraction of each substance are as follows: ZrO215 parts of nano-powder, 4 parts of ZnO nanoparticle;It should ZrO2The partial size of nano-powder is 20nm.
Filler B is anionic additive, wherein the tourmaline nano particle diameter is 100nm.
Tourmaline is a kind of natural electrode with similar to magnet poles, and tourmaline is widely used in environmental protection, day The often numerous areas such as life, for example, tourmaline powder is added in artificial silk, since tourmaline powder has positive and negative electrode, After human contact, countless weak currents can be generated in skin surface, stimulate blood circulation, form negative ion effect;However, In this field, tourmaline is directly used in textile, electronegative ion can not be played well.Technical solution of the present invention In, by having obtained tourmaline nano particle and ZnO nanoparticle dispersant, calcining filler B, then having been added again Enter in polyester fiber.By above-mentioned mixing, calcination process, the uniformity of anion emission is substantially increased, produces expectation not The technical effect arrived.
Preferably, in filler B, the mass fraction of each substance are as follows: 17 parts of tourmaline nano particle, 11 parts of ZnO nanoparticle.
Filler C is electromagnetic shielding filler, wherein the NiFe2O4The partial size of nanoparticle is 30~50nm;
Preferably, in filler C, the mass fraction of each substance are as follows: NiFe2O45 parts of nanoparticle, 2 parts of ZnO nanoparticle;
The NiFe2O4Nanoparticle is synthesized by hydro-thermal method, specifically: weigh 10g polyethylene glycol and 7g dodecyl Ammonium benzene sulfonate is dissolved in 20ml distilled water, and the Fe (NO of 2mol is then added3)3·9H2O, the Ni (NO of 1mol3)2·6H2O, with urine It is 11.5 that element, which adjusts pH value, stirs evenly, mixed liquor is transferred in autoclave, 20h is reacted at 270 DEG C, then natural cooling, After separation of solid and liquid, washing, drying, solid matter is calcined into 10h in the case where 400min is warming up to 870 DEG C, obtains NiFe2O4Nanometer Particle.
Further explanation is made to the present invention below with reference to embodiment.
Embodiment 1
It is a kind of with anion, far infrared, healthcare function polyester fiber, the polyester fiber is using polyester as substrate, to fill out Expect that A, filler B, filler C are additive, by melting blended be prepared;In terms of content, raw material is according to weight percent Include: 3% filler A, 8% filler B, 4% filler C, surplus be polyester.
Filler A includes: ZrO2Nano-powder and ZnO nanoparticle;Filler B includes: tourmaline nano particle and ZnO Nanoparticle;Filler C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.
Above-mentioned ZnO nanoparticle partial size is 30nm.
Filler A is far infrared additive, wherein the ZrO2Nano-powder is to be prepared by ultrasonic microemulsion liquid method;It should ZrO2The partial size of nano-powder is 20nm;In filler A, the mass fraction of each substance are as follows: ZrO215 parts of nano-powder, ZnO nano grain 4 parts of son.
Filler B is anionic additive, wherein the tourmaline nano particle diameter is 100nm;In filler B, each object The mass fraction of matter are as follows: 17 parts of tourmaline nano particle, 11 parts of ZnO nanoparticle.
Filler C is electromagnetic shielding filler, wherein the NiFe2O4The partial size of nanoparticle is 30~50nm;In filler C, The mass fraction of each substance are as follows: NiFe2O45 parts of nanoparticle, 2 parts of ZnO nanoparticle.
The preparation process of the filler A, filler B, filler C are as follows:
Step 1, NiFe is prepared2O4Nanoparticle
It weighs 10g polyethylene glycol and 7g dodecyl benzene sulfonic acid ammonium is dissolved in 20ml distilled water, the Fe of 2mol is then added (NO3)3·9H2O, the Ni (NO of 1mol3)2·6H2O, adjusting pH value with urea is 11.5, stirs evenly, mixed liquor is transferred to height It presses in kettle, 20h is reacted at 270 DEG C, then natural cooling, after separation of solid and liquid, washing, drying, solid matter is existed 400min is warming up at 870 DEG C and calcines 10h, obtains NiFe2O4Nanoparticle;
Step 2 prepares zirconium oxide presoma
By the ZrOCl of 720g/L2·8H2The ethylenediamine tetra-acetic acid of O and 94g/L is mixed according to volume ratio 2:1, is vigorously stirred 30min make its be uniformly mixed, obtain transparent micro emulsion, then with ammonium hydroxide adjust pH value be 11.4, the ultrasound 14min at 84 DEG C, Ultrasonic power is 20KHz, obtains clear gel, is then washed with distilled water to AgNO3Solution inspection does not measure Cl?, then use Ethanol washing 3 times, the zirconium oxide presoma after washing is put into thermostatic drying chamber, in 60 DEG C of dry 15h;
Step 3 prepares filler
Zirconium oxide presoma, ZnO nanoparticle and titanate coupling agent are add to deionized water, are sufficiently stirred It is even, obtain far infrared additive slurry, be then baked to, under nitrogen protection in 360 DEG C of calcining 5h, pulverize to get Filler A;
Tourmaline nano particle, ZnO nanoparticle and titanate coupling agent are add to deionized water, are sufficiently stirred It is even, obtain anionic additive slurry, be then baked to, under nitrogen protection in 480 DEG C of calcining 6h, pulverize to get Filler B;
By NiFe2O4Nanoparticle, ZnO nanoparticle and titanate coupling agent are add to deionized water, and are sufficiently stirred It is even, electromagnetic shielding additive slurry is obtained, is then baked to, under nitrogen protection in 450 DEG C of calcining 5h, pulverizes, i.e., Obtain filler C;
The preparation process of the polyester fiber are as follows:
Firstly, filler A, filler B, filler C and ethylene glycol are mixed, ultrasound 5h at room temperature after stirring obtains mixed liquor; Then mixed liquor and p-phthalic acid, catalyst aid are esterified, polymerize, obtains polyester master particle;Wherein, esterification temperature is 280 DEG C, pressure 270kPa, polycondensation reaction is carried out when esterification yield reaches greater than 95.5%, condensation temperature is 2850 DEG C, is evacuated to 22MPa, when polycondensation to inherent viscosity is 0.74 deciliter/gram, discharging, blank;
Polyester master particle is melted, filter is then fed into and is filtered, after metering, into spinning pack, then will be sprayed Tow carry out it is cooling, oil, preoriented yarn is wound into after deflector roll, wherein spinning temperature is 290 DEG C, and spinning speed is 3200m/min;
Polyester preoriented yarn can be prepared into the polyester fiber after a roller, hot tank, two rollers, scroll tube, winding, wherein Draft speed is 480m/min, and draw ratio 3.1, a roll temperature is 90 DEG C, and two roll temperatures are 140 DEG C.
The far-infrared radiated property of fiber is characterized by measuring the normal emittance of polyester fiber in the present embodiment, is examined The result shows that its normal emittance is 0.94, quasi- about the assessment of bids of far infrared performance according to this field, normal emittance is more than or equal to 0.8 can be assessed as far-infrared textiles, and the composite fibre in the present embodiment is met the requirements of the standard;
Measure the anionic property of polyester fiber in the present embodiment:
It is detected using air ion concentration relative standard's measuring device, the polyester fiber that the application is obtained and common Polyester fiber is cut into 10 × 10cm respectively2Size, apart from above-mentioned detection device 6.5cm2Air inlet 2mm or so, measure air Middle negative ion concentration, the polyester fiber anion emission number for obtaining the application is 4683 anion/cm3, and conventional polyester The negative ion concentration of fiber is substantially zeroed, illustrates that the polyester fiber of the application has good anion emission performance.
The absorbing property of polyester fiber in the present embodiment is measured, maximum absorption peak is -24.6dB, and the bandwidth of -5dB is 2500MHz has good electromagnetic shielding performance.
Embodiment 2
It is a kind of with anion, far infrared, healthcare function polyester fiber, the polyester fiber is using polyester as substrate, to fill out Expect that A, filler B, filler C are additive, by melting blended be prepared;In terms of content, raw material is according to weight percent Include: 9% filler A, 12% filler B, 10% filler C, surplus be polyester.
Filler A includes: ZrO2Nano-powder and ZnO nanoparticle;Filler B includes: tourmaline nano particle and ZnO Nanoparticle;Filler C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.
Above-mentioned ZnO nanoparticle partial size is 30nm.
Filler A is far infrared additive, wherein the ZrO2Nano-powder is to be prepared by ultrasonic microemulsion liquid method;It should ZrO2The partial size of nano-powder is 20nm;In filler A, the mass fraction of each substance are as follows: ZrO215 parts of nano-powder, ZnO nano grain 4 parts of son.
Filler B is anionic additive, wherein the tourmaline nano particle diameter is 100nm;In filler B, each object The mass fraction of matter are as follows: 17 parts of tourmaline nano particle, 11 parts of ZnO nanoparticle.
Filler C is electromagnetic shielding filler, wherein the NiFe2O4The partial size of nanoparticle is 30~50nm;In filler C, The mass fraction of each substance are as follows: NiFe2O45 parts of nanoparticle, 2 parts of ZnO nanoparticle.
The preparation process of the filler A, filler B, filler C are as follows:
Step 1, NiFe is prepared2O4Nanoparticle
It weighs 10g polyethylene glycol and 7g dodecyl benzene sulfonic acid ammonium is dissolved in 20ml distilled water, the Fe of 2mol is then added (NO3)3·9H2O, the Ni (NO of 1mol3)2·6H2O, adjusting pH value with urea is 11.5, stirs evenly, mixed liquor is transferred to height It presses in kettle, 20h is reacted at 270 DEG C, then natural cooling, after separation of solid and liquid, washing, drying, solid matter is existed 400min is warming up at 870 DEG C and calcines 10h, obtains NiFe2O4Nanoparticle;
Step 2 prepares zirconium oxide presoma
By the ZrOCl of 720g/L2·8H2The ethylenediamine tetra-acetic acid of O and 94g/L is mixed according to volume ratio 2:1, is vigorously stirred 30min make its be uniformly mixed, obtain transparent micro emulsion, then with ammonium hydroxide adjust pH value be 11.4, the ultrasound 14min at 84 DEG C, Ultrasonic power is 20KHz, obtains clear gel, is then washed with distilled water to AgNO3Solution inspection does not measure Cl?, then use Ethanol washing 3 times, the zirconium oxide presoma after washing is put into thermostatic drying chamber, in 60 DEG C of dry 15h;
Step 3 prepares filler
Zirconium oxide presoma, ZnO nanoparticle and titanate coupling agent are add to deionized water, are sufficiently stirred It is even, obtain far infrared additive slurry, be then baked to, under nitrogen protection in 360 DEG C of calcining 5h, pulverize to get Filler A;
Tourmaline nano particle, ZnO nanoparticle and titanate coupling agent are add to deionized water, are sufficiently stirred It is even, obtain anionic additive slurry, be then baked to, under nitrogen protection in 480 DEG C of calcining 6h, pulverize to get Filler B;
By NiFe2O4Nanoparticle, ZnO nanoparticle and titanate coupling agent are add to deionized water, and are sufficiently stirred It is even, electromagnetic shielding additive slurry is obtained, is then baked to, under nitrogen protection in 450 DEG C of calcining 5h, pulverizes, i.e., Obtain filler C;
The preparation process of the polyester fiber are as follows:
Firstly, filler A, filler B, filler C and ethylene glycol are mixed, ultrasound 5h at room temperature after stirring obtains mixed liquor; Then mixed liquor and p-phthalic acid, catalyst aid are esterified, polymerize, obtains polyester master particle;Wherein, esterification temperature is 280 DEG C, pressure 270kPa, polycondensation reaction is carried out when esterification yield reaches greater than 95.5%, condensation temperature is 2850 DEG C, is evacuated to 22MPa, when polycondensation to inherent viscosity is 0.74 deciliter/gram, discharging, blank;
Polyester master particle is melted, filter is then fed into and is filtered, after metering, into spinning pack, then will be sprayed Tow carry out it is cooling, oil, preoriented yarn is wound into after deflector roll, wherein spinning temperature is 290 DEG C, and spinning speed is 3200m/min;
Polyester preoriented yarn can be prepared into the polyester fiber after a roller, hot tank, two rollers, scroll tube, winding, wherein Draft speed is 480m/min, and draw ratio 3.1, a roll temperature is 90 DEG C, and two roll temperatures are 140 DEG C.
The far-infrared radiated property of fiber is characterized by measuring the normal emittance of polyester fiber in the present embodiment, is examined The result shows that its normal emittance is 0.93, quasi- about the assessment of bids of far infrared performance according to this field, normal emittance is more than or equal to 0.8 can be assessed as far-infrared textiles, and the composite fibre in the present embodiment is met the requirements of the standard;
Measure the anionic property of polyester fiber in the present embodiment:
It is detected using air ion concentration relative standard's measuring device, the polyester fiber that the application is obtained and common Polyester fiber is cut into 10 × 10cm respectively2Size, apart from above-mentioned detection device 6.5cm2Air inlet 2mm or so, measure air Middle negative ion concentration, the polyester fiber anion emission number for obtaining the application is 4521 anion/cm3, and conventional polyester The negative ion concentration of fiber is substantially zeroed, illustrates that the polyester fiber of the application has good anion emission performance.
The absorbing property of polyester fiber in the present embodiment is measured, maximum absorption peak is -23.9dB, and the bandwidth of -5dB is 2600MHz has good electromagnetic shielding performance.
Embodiment 3
It is a kind of with anion, far infrared, healthcare function polyester fiber, the polyester fiber is using polyester as substrate, to fill out Expect that A, filler B, filler C are additive, by melting blended be prepared;In terms of content, raw material is according to weight percent Include: 7% filler A, 11% filler B, 7% filler C, surplus be polyester.
Filler A includes: ZrO2Nano-powder and ZnO nanoparticle;Filler B includes: tourmaline nano particle and ZnO Nanoparticle;Filler C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.
Above-mentioned ZnO nanoparticle partial size is 30nm.
Filler A is far infrared additive, wherein the ZrO2Nano-powder is to be prepared by ultrasonic microemulsion liquid method;It should ZrO2The partial size of nano-powder is 20nm;In filler A, the mass fraction of each substance are as follows: ZrO215 parts of nano-powder, ZnO nano grain 4 parts of son.
Filler B is anionic additive, wherein the tourmaline nano particle diameter is 100nm;In filler B, each object The mass fraction of matter are as follows: 17 parts of tourmaline nano particle, 11 parts of ZnO nanoparticle.
Filler C is electromagnetic shielding filler, wherein the NiFe2O4The partial size of nanoparticle is 30~50nm;In filler C, The mass fraction of each substance are as follows: NiFe2O45 parts of nanoparticle, 2 parts of ZnO nanoparticle.
The preparation process of the filler A, filler B, filler C are as follows:
Step 1, NiFe is prepared2O4Nanoparticle
It weighs 10g polyethylene glycol and 7g dodecyl benzene sulfonic acid ammonium is dissolved in 20ml distilled water, the Fe of 2mol is then added (NO3)3·9H2O, the Ni (NO of 1mol3)2·6H2O, adjusting pH value with urea is 11.5, stirs evenly, mixed liquor is transferred to height It presses in kettle, 20h is reacted at 270 DEG C, then natural cooling, after separation of solid and liquid, washing, drying, solid matter is existed 400min is warming up at 870 DEG C and calcines 10h, obtains NiFe2O4Nanoparticle;
Step 2 prepares zirconium oxide presoma
By the ZrOCl of 720g/L2·8H2The ethylenediamine tetra-acetic acid of O and 94g/L is mixed according to volume ratio 2:1, is vigorously stirred 30min make its be uniformly mixed, obtain transparent micro emulsion, then with ammonium hydroxide adjust pH value be 11.4, the ultrasound 14min at 84 DEG C, Ultrasonic power is 20KHz, obtains clear gel, is then washed with distilled water to AgNO3Solution inspection does not measure Cl?, then use Ethanol washing 3 times, the zirconium oxide presoma after washing is put into thermostatic drying chamber, in 60 DEG C of dry 15h;
Step 3 prepares filler
Zirconium oxide presoma, ZnO nanoparticle and titanate coupling agent are add to deionized water, are sufficiently stirred It is even, obtain far infrared additive slurry, be then baked to, under nitrogen protection in 360 DEG C of calcining 5h, pulverize to get Filler A;
Tourmaline nano particle, ZnO nanoparticle and titanate coupling agent are add to deionized water, are sufficiently stirred It is even, obtain anionic additive slurry, be then baked to, under nitrogen protection in 480 DEG C of calcining 6h, pulverize to get Filler B;
By NiFe2O4Nanoparticle, ZnO nanoparticle and titanate coupling agent are add to deionized water, and are sufficiently stirred It is even, electromagnetic shielding additive slurry is obtained, is then baked to, under nitrogen protection in 450 DEG C of calcining 5h, pulverizes, i.e., Obtain filler C;
The preparation process of the polyester fiber are as follows:
Firstly, filler A, filler B, filler C and ethylene glycol are mixed, ultrasound 5h at room temperature after stirring obtains mixed liquor; Then mixed liquor and p-phthalic acid, catalyst aid are esterified, polymerize, obtains polyester master particle;Wherein, esterification temperature is 280 DEG C, pressure 270kPa, polycondensation reaction is carried out when esterification yield reaches greater than 95.5%, condensation temperature is 2850 DEG C, is evacuated to 22MPa, when polycondensation to inherent viscosity is 0.74 deciliter/gram, discharging, blank;
Polyester master particle is melted, filter is then fed into and is filtered, after metering, into spinning pack, then will be sprayed Tow carry out it is cooling, oil, preoriented yarn is wound into after deflector roll, wherein spinning temperature is 290 DEG C, and spinning speed is 3200m/min;
Polyester preoriented yarn can be prepared into the polyester fiber after a roller, hot tank, two rollers, scroll tube, winding, wherein Draft speed is 480m/min, and draw ratio 3.1, a roll temperature is 90 DEG C, and two roll temperatures are 140 DEG C.
The far-infrared radiated property of fiber is characterized by measuring the normal emittance of polyester fiber in the present embodiment, is examined The result shows that its normal emittance is 0.91, quasi- about the assessment of bids of far infrared performance according to this field, normal emittance is more than or equal to 0.8 can be assessed as far-infrared textiles, and the composite fibre in the present embodiment is met the requirements of the standard;
Measure the anionic property of polyester fiber in the present embodiment:
It is detected using air ion concentration relative standard's measuring device, the polyester fiber that the application is obtained and common Polyester fiber is cut into 10 × 10cm respectively2Size, apart from above-mentioned detection device 6.5cm2Air inlet 2mm or so, measure air Middle negative ion concentration, the polyester fiber anion emission number for obtaining the application is 3674 anion/cm3, and conventional polyester The negative ion concentration of fiber is substantially zeroed, illustrates that the polyester fiber of the application has good anion emission performance.
The absorbing property of polyester fiber in the present embodiment is measured, maximum absorption peak is -22.9dB, and the bandwidth of -5dB is 2400MHz has good electromagnetic shielding performance.
The foregoing is merely preferred modes of the invention, are not intended to limit the invention, all in spirit and original of the invention Within then, any modification, equivalent replacement, improvement and so on be should all be included in the protection scope of the present invention.

Claims (10)

1. it is a kind of with anion, far infrared, healthcare function polyester fiber, the polyester fiber is using polyester as substrate, with filler A, filler B, filler C are additive, by melting blended be prepared;It is characterized in that, the filler A includes: ZrO2Nanometer Powder and ZnO nanoparticle;The filler B includes: tourmaline nano particle and ZnO nanoparticle;The filler C includes: NiFe2O4Nanoparticle and ZnO nanoparticle.
2. polyester fiber according to claim 1, which is characterized in that the polyester fiber, in terms of content, raw material is pressed According to weight percent include: 3~9% filler A, 8~12% filler B, 4~10% filler C, surplus be polyester.
3. polyester fiber according to claim 2, which is characterized in that the filler A, filler B, in filler C, ZnO nano Particle diameter is 30nm.
4. polyester fiber according to claim 3, which is characterized in that in filler A, the ZrO2Nano-powder is to pass through The preparation of ultrasonic microemulsion liquid method;The ZrO2The partial size of nano-powder is 20nm.
5. polyester fiber according to claim 4, which is characterized in that in filler A, the mass fraction of each substance are as follows: ZrO2It receives 15 parts of rice flour body, 4 parts of ZnO nanoparticle.
6. polyester fiber according to claim 5, which is characterized in that the preparation process of the filler A are as follows:
Step 1 prepares zirconium oxide presoma
By the ZrOCl of 720g/L2·8H2The ethylenediamine tetra-acetic acid of O and 94g/L is mixed according to volume ratio 2:1, is vigorously stirred 30min It is uniformly mixed it, obtains transparent micro emulsion, then adjusting pH value with ammonium hydroxide is 11.4, ultrasound 14min, ultrasonic function at 84 DEG C Rate is 20KHz, obtains clear gel, is then washed with distilled water to AgNO3Solution inspection does not measure Cl?, then washed with ethyl alcohol It washs 3 times, the zirconium oxide presoma after washing is put into thermostatic drying chamber, in 60 DEG C of dry 15h;
Step 2 prepares filler A
Zirconium oxide presoma, ZnO nanoparticle and titanate coupling agent are add to deionized water, stirred, is obtained It to far infrared additive slurry, is then baked to, under nitrogen protection in 360 DEG C of calcining 5h, pulverizes to get filler A.
7. polyester fiber according to claim 3, which is characterized in that in filler B, the tourmaline nano particle diameter is 100nm。
8. polyester fiber according to claim 7, which is characterized in that in filler B, the mass fraction of each substance are as follows: electrical 17 parts of stone nano particle, 11 parts of ZnO nanoparticle.
9. polyester fiber according to claim 3, which is characterized in that in filler C, the NiFe2O4The partial size of nanoparticle For 30~50nm;In filler C, the mass fraction of each substance are as follows: NiFe2O45 parts of nanoparticle, 2 parts of ZnO nanoparticle.
10. polyester fiber according to claim 9, which is characterized in that the preparation process of the filler C are as follows:
Step 1, NiFe is prepared2O4Nanoparticle
It weighs 10g polyethylene glycol and 7g dodecyl benzene sulfonic acid ammonium is dissolved in 20ml distilled water, the Fe of 2mol is then added (NO3)3·9H2O, the Ni (NO of 1mol3)2·6H2O, adjusting pH value with urea is 11.5, stirs evenly, mixed liquor is transferred to height It presses in kettle, 20h is reacted at 270 DEG C, then natural cooling, after separation of solid and liquid, washing, drying, solid matter is existed 400min is warming up at 870 DEG C and calcines 10h, obtains NiFe2O4Nanoparticle;
Step 2 prepares filler C
By NiFe2O4Nanoparticle, ZnO nanoparticle and titanate coupling agent are add to deionized water, and are stirred, Electromagnetic shielding additive slurry is obtained, is then baked to, under nitrogen protection in 450 DEG C of calcining 5h, pulverizes to get filling out Expect C.
CN201810745742.5A 2018-07-09 2018-07-09 It is a kind of with anion, far infrared, healthcare function polyester fiber Pending CN109137127A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115197543A (en) * 2021-04-14 2022-10-18 上海沪正实业有限公司 Filling master batch with anti-mite far infrared emission function and application thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104045336A (en) * 2014-07-04 2014-09-17 西北师范大学 Preparation method of nickel ferrite magnetic nanofiber material
CN105820796A (en) * 2016-04-25 2016-08-03 中国科学院西安光学精密机械研究所 Preparation method of magnetic-alloy-loaded porous carbon sphere composite wave-absorbing material
CN107083579A (en) * 2017-06-07 2017-08-22 广州市中诚新型材料科技有限公司 Anion, far infrared, antibiosis anti-acarien composite polyester fiber and its manufacture method
CN107142546A (en) * 2017-06-07 2017-09-08 广州市中诚新型材料科技有限公司 The compound polyester functional fibre of a kind of far infrared, antibacterial mite-removing and its manufacture method

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104045336A (en) * 2014-07-04 2014-09-17 西北师范大学 Preparation method of nickel ferrite magnetic nanofiber material
CN105820796A (en) * 2016-04-25 2016-08-03 中国科学院西安光学精密机械研究所 Preparation method of magnetic-alloy-loaded porous carbon sphere composite wave-absorbing material
CN107083579A (en) * 2017-06-07 2017-08-22 广州市中诚新型材料科技有限公司 Anion, far infrared, antibiosis anti-acarien composite polyester fiber and its manufacture method
CN107142546A (en) * 2017-06-07 2017-09-08 广州市中诚新型材料科技有限公司 The compound polyester functional fibre of a kind of far infrared, antibacterial mite-removing and its manufacture method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
欧阳兆辉: ""镍铁氧体与二氧化钛孔材料的研究"", 《中国博士学位论文全文数据库 工程科技Ⅰ辑》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115197543A (en) * 2021-04-14 2022-10-18 上海沪正实业有限公司 Filling master batch with anti-mite far infrared emission function and application thereof

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Application publication date: 20190104