CN105297169A - Colored special-shaped super fine denier polyester monofilaments and production method thereof - Google Patents

Colored special-shaped super fine denier polyester monofilaments and production method thereof Download PDF

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CN105297169A
CN105297169A CN201510685136.5A CN201510685136A CN105297169A CN 105297169 A CN105297169 A CN 105297169A CN 201510685136 A CN201510685136 A CN 201510685136A CN 105297169 A CN105297169 A CN 105297169A
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denier polyester
polyester monofilament
superfine denier
colored
production method
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张志明
陈龙
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ZHEJIANG JINXIA NEW MATERIALS TECHNOLOGY Co Ltd
JINXIA CHEMICAL FIBERS CO Ltd SHANGHAI
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ZHEJIANG JINXIA NEW MATERIALS TECHNOLOGY Co Ltd
JINXIA CHEMICAL FIBERS CO Ltd SHANGHAI
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Abstract

The invention relates to colored special-shaped super fine denier polyester monofilaments and a production method thereof. The colored special-shaped super fine denier polyester monofilaments are prepared from, by mass, 1-5% of anti-aging capsules, 5-10% of pigment, 5-10% of PEN slices, 1-3% of a dispersing agent and the balance polyester slices. The PEN slices, the polyester slices, the anti-aging capsules, the pigment and the dispersing agent are extruded and mixed together through a screw machine and then melted, melt is prepared and subjected to melt spinning through a special-shaped spinneret plate, and the colored special-shaped super fine denier polyester monofilaments are obtained. Due to the fact that PEN is added, the heat resistance of fibers is improved, and thus the roll sticking phenomenon is avoided when the heat setting temperature is higher than 245 DEG C; meanwhile, due to the higher heat setting temperature, disorientation of an orientation structure of an amorphous area is accelerated, the internal stress of the fibers is reduced, and thus the dimension stability of the fibers is improved; the setting temperature is raised, the mobility of macromolecular chains in the fiber structure is enhanced, the degree of crystallinity is increased, the content of an amorphous area is reduced, and the boiling water shrinkage is reduced.

Description

A kind of colored profiled superfine denier polyester monofilament and production method thereof
[technical field]
The present invention relates to polyester monofilament technical field, specifically, is a kind of colored profiled superfine denier polyester monofilament and production method thereof.
[background technology]
Chinese Patent Application No. 200910027027.9 relates to a kind of melt direct spinning superfine denier terylene FDY filament and preparation technology thereof, this superfine denier terylene FDY filament is according to fused mass directly spinning One-step production route, pore diameter is used to be 0.15-0.2MM, L/D=2.6-3.6, plate surface diameter is the spinnerets of 70-90MM, fiber cooling zone is installed radome fairing and is adopted twice oil feeding system directly to produce ultra-fine FDY silk, and gained filament number DPF is 0.3-0.6, and a synnema hole count is 144F-192F; The process route adopted makes processing cost significantly reduce while the inherent quality of improving product, has the ability replacing import like product.
Chinese Patent Application No. 201120546341.0 relates to superfine denier polyester elastic filament, and feature is: its cross sectional shape is V-shaped or T-shaped, and its filament number is 0.25-0.45dtex; Advantage is: superfine denier polyester elastic filament, has warming, the advantage such as good permeability, feel are smooth, light weight, waterproof.
Chinese Patent Application No. 200710026149.7 relates to a kind of preparation method of ultra-fine denier polyester filament yarn.The process employs lateral blowing process for cooling, by the height of adjustment zone of silence, the arrangement mode increasing annealer and improvement spinneret hole and oiling method in spinning process, the ultra-fine denier polyester filament yarn that a kind of filament number is 0.2 ~ 0.5D.P.F successfully can be produced; Gained polyester filament has physical characteristic and the processing characteristics of excellent spinnability and excellence.
Chinese Patent Application No. 201310090354.5 relates to a kind of production method of colored superfine denier polyester pre-oriented yarn, polyethylene terephthalate and terylene Color master batch are carried out crystallization and drying respectively, then by its melting, then by pre-filtering and secondary filter, ring quenching, oil, seal wire, increase internet pricing, coiling and molding; Terylene Color master batch and polyethylene terephthalate are combined, eliminate the step of follow-up dyeing, decrease in dyeing course the sewage needing electric energy and the discharge consumed, reach the object of environmental protection, the call that response national energy-saving reduces discharging, obtained ultra-fine denier polyester filament yarn has preferably soft feel, there is wax-like sense simultaneously, even comparable wool, silk also want soft, and have fine gas permeability and warmth retention property after woven into fabric, its product is mainly used in high-grade fabric.
Chinese Patent Application No. 201110380484.3 relates to a kind of manufacturing technique of hollow micro-fine terylene denier fiber, it is characterized in that comprising the following steps: a) raw material are terylene chips; B) terylene chips is carried out drying through crystallizing and drying machine; C) dried terylene chips is expelled in screw extruder by calibrated shot machine and carries out melting; D) volume of melt is controlled by spinning oil measuring pump and spinning pump; E) on spinning machine, spinning is carried out; Undertaken being wound into spinning cake by fully automatic high-speed up-coiler after spinning; F) spinning cake after winding is placed between balance and balances; G) spinning cake after balance carries out adding bullet on conventional elasticizer; The filament number achieving fiber is less than 0.5dpf.
Chinese Patent Application No. 201120483660.1 relates to synthetic fiber field, has greatly light terylene six leaf special-shaped monofilament specifically for one, solves in prior art aspect problems such as there is dyeing difference.In monofilament, be provided with core bore, the cross section of monofilament is sexfoil, and six leaves of cross section distribute at circumferencial direction by the order of leaf I, leaf II, leaf III, leaf IV, leaf V, leaf VI.Core bore is that room is in monofilament center, the cross section of core bore is hexagon, each end of blade of sexfoil is semicircle, and the area of the cross section of core bore is 1/10 ~ 1/20 of monofilament total cross sectional area, and the angle between adjacent two leaves of this cross section is 10 ° ~ 150 °.Orthohexagonal spinnerets direct fabrics make greatly light terylene six leaf special-shaped monofilament by be sexfoil and intermediate cross-section be singe screw and cross section to adopt one-component to have greatly light polyester raw material; This fiber has the advantages such as dyeing is fast through weaving the fabric made.
Chinese Patent Application No. 201410754263.1 relates to the production method of the flat special-shaped polyester industrial filament yarn of a kind of fused mass directly spinning, adopt spinneret orifice cross section to be that special " one " font spinnerets processes, obtain product by melt liquid-phase tackifying-melt spinning-stretching and winding molding production process; The production method adopted shortens the reaction time, effectively shorten technological process, raise the efficiency, reduce energy consumption, the basis keeping general industry silk advantage substantially increases coherent, and owing to having approximate rectangular cross section, the space between strand is little, contact area increases, arrange more smooth compact, make strand have outstanding hair orthostatic and high coherent, preferably bending rigidity and pliability.This product is due to close-packed arrays between monofilament, and flatness improves, and the aesthetics after blade coating also improves greatly, and reduces production process, simplifies production technology.
Poly-NDA second two (alcohol) ester (PEN) is a kind of high-performance novel polyester that a kind of performance is more better than polyethylene terephthalate (PET).PEN has excellent barrier properties for gases, water proofing property, uvioresistant, heat resistance, and chemical proofing and radiation resistance, can be used as PET, the activeness and quietness agent of the high polymers such as PC, and purposes is very extensive.China Patent Publication No. CN102660018A and China Patent Publication No. CN202968797U discloses the application in the fibre of this material to improve heat resistance or the barrier property of fiber, but does not relate to it and PET is blended prepares colored non-conventional fiber; Chinese patent CN1211204C discloses the production method of the blended or copolymerization film of a kind of PET/PEN, but does not relate to the preparation of fiber.
[summary of the invention]
The object of the invention is to overcome the deficiencies in the prior art, a kind of colored profiled superfine denier polyester monofilament and production method thereof are provided.
The object of the invention is to be achieved through the following technical solutions:
A kind of colored profiled superfine denier polyester monofilament, its material quality percentage is:
Described PEN section is poly-NDA diethylester section, and PEN is writing a Chinese character in simplified form of poly-NDA diethylester.
The mass percent of described anti-aging capsule is 3%.
The mass percent of described pigment is 7%.
The mass percent of described dispersant is 2%.
Described pigment is carbon black, AZO pigments, one or more in phthalocyanine color or Heterocyclics Pigments.
Described dispersant is Tissuemat E, the one in fatty acid ester or calcium stearate.
The preparation method of described anti-aging capsule, its concrete steps are:
A () is to the preparation of dihydroxy Pyrogentisinic Acid base phosphine
With Phenylphosphine and paraformaldehyde for raw material, with water and isopropyl alcohol mixture for solvent, under catalyst action, affine addition reaction occurs, controlling reaction temperature is 35 ~ 50 DEG C, and the reaction time is 3 ~ 4h, prepare dihydroxymethyl phenyl phosphine, again at 85 ~ 95 DEG C, the mixed solution adding hydrogen peroxide and the concentrated sulfuric acid is strong oxidizer, oxidation 45 ~ 60min, prepare dihydroxymethyl phenyl phosphine oxide, by the hydroquinol base phosphine of synthesis, bromine water and iron powder add in reaction vessel, filter after being heated to 65 ~ 75 DEG C of reaction 0.5 ~ 1.75h and obtain kermesinus product, in the potassium hydroxide it being joined at normal temperatures 0.2mol/L and potassium ethoxide solution, in 80 ~ 95 DEG C of reaction 1 ~ 3h after dissolving completely, again product is recrystallized in steam bath, in triplicate, obtain white to dihydroxy Pyrogentisinic Acid base phosphine,
Described Phenylphosphine and the mol ratio of paraformaldehyde are 1: 2.2;
Catalyst is vanadic anhydride, and described Phenylphosphine and catalyst molar ratio value are 1: 0.035;
Described water and the volume ratio of isopropyl alcohol are 1: 0.95;
The mass fraction of described paraformaldehyde is 12%;
Described strong oxidizer and the mass values of Phenylphosphine are 1: 2.9;
The mass fraction of described hydrogen peroxide is 22%;
In described hydrogen peroxide and concentrated sulfuric acid solution, hydrogen peroxide and concentrated sulfuric acid volume ratio are 1: 2;
Described hydroquinol base phosphine, the mol ratio 1: 1.2: 0.01 of bromine water and iron powder;
Described potassium hydroxide and the mol ratio of potassium ethoxide are 1: 3.5;
The preparation of (b) ortho-nitraniline diazol
By ortho-nitraniline strong agitation be quickly cooled to 0 DEG C in the red fuming nitric acid (RFNA) of 12mol/L, after 1.5h, add the 4mol/L potassium nitrite aqueous solution, filter react 0.5 ~ 1.0h at 0 ~ 5 DEG C after, obtain ortho-nitraniline diazol;
The preparation of (c) azo-compound
That step (a) is prepared is added in the mixed solution of isopropyl alcohol and distilled water to dihydroxy Pyrogentisinic Acid base phosphine, keep solution temperature 5 ~ 10 DEG C, ortho-nitraniline diazol prepared by gradation instillation step (b), suction filtration, washing, dry azo-compound, it is rediance crystal;
Isopropyl alcohol in described isopropyl alcohol and the mixed solution of distilled water and the volume ratio of distilled water are 1: 0.75;
Described is 4% to dihydroxy Pyrogentisinic Acid base phosphine at the mass fraction of the mixed solution of isopropyl alcohol and distilled water;
Described is 1: 1 to the mol ratio of dihydroxy Pyrogentisinic Acid base phosphine and ortho-nitraniline diazol;
(d) ageing-resistant preparation
Under nitrogen protection, azo-compound step (c) prepared joins in the water of the NaOH of 3.0mol/L and the mixed solution of ethanol, stir also gradation and add reductant thiourea dioxide, room temperature is cooled to react 2h at 60 ~ 65 DEG C after, add nitric acid pH to regulate between 5 ~ 6, suction filtration, dry in the shade, dry again after recrystallization, obtain functional modifier crude product, then by functional modifier crude product, hydrofluoric acid and red fuming nitric acid (RFNA) add in reaction vessel, after being heated to 65 ~ 75 DEG C of reaction 0.5 ~ 1.0h, filtration obtains Off-white product, through cooling suction filtration, dry in the shade, recrystallization and drying, obtain age resister,
Water in described water and the mixed solution of ethanol and the volume ratio of ethanol are 1: 1;
Described thiourea dioxide and the mol ratio of azo-compound are 1: 0.5;
Described functional modifier crude product, the mol ratio 1: 1.2: 0.01 of hydrofluoric acid and red fuming nitric acid (RFNA);
The preparation of (e) anti-aging capsule
Take deionized water as solvent, age resister dispersion in a solvent, whipping temp is normal temperature, controlling whipping process medium-rate is 800 ~ 1200r/min, the dispersed with stirring time is 30 ~ 45min, age resister molecule is enable to form suspension system in aqueous, and then add hydroxyethylcellulose and dissolve, carry out high-speed stirred dispersion again, whipping temp is 45 ~ 55 DEG C, stir speed (S.S.) is 2000 ~ 3300r/min, mixing time is 20 ~ 30min, and then add BTCA carry out chitin be cross-linked, slaking 30min is carried out again under 65 ~ 80 DEG C of conditions, filtration obtains thick modification capsule, after carrying out vacuumize 24h at 60 DEG C again, obtain ageing-resistant anti-aging capsule, its sandwich layer is age resister, and cystoblast is hydroxyethylcellulose materials, and wherein, the Thickness Ratio of cystoblast and sandwich layer is 1: 15.
Described age resister addition is 4.5% relative to the mass fraction of water;
Described hydroxyethylcellulose addition is 2.7% relative to the mass fraction of water;
The weight average molecular weight of described hydroxyethylcellulose is 20000 ~ 25000, and molar substitution is 1.8 ~ 1.9.
Described BTCA is 0.45% relative to the mass fraction of chitin.
A production method for colored profiled superfine denier polyester monofilament, its concrete steps are:
Cut into slices by PEN, terylene chips, anti-aging capsule, pigment, dispersant, melting after screw machine extruding is blended, makes melt, carries out melt spinning through profile spinneret, obtain colored profiled superfine denier polyester monofilament.
The shape of described spinnerets is selected from in-line, trilobal, triangle, the one in cross or five blade profiles.
Profile spinneret is triangle spinnerets, and its imitative triangle spinneret orifice is evenly distributed on triangle spinnerets, the cross sectional shape of imitative triangle spinneret orifice be equilateral triangle change circular arc into, circular arc is connected with leg-of-mutton both sides.
The number of degrees of described circular arc are 120 degree.
Compared with prior art, good effect of the present invention is:
PEN adds, and improves the heat resistance of fiber, does not occur roll banding phenomenon when making heat setting temperature more than 245 degree, for the preparation of the section of fiber without the need to solid-phase tack producing, also can use conventional method spinning without the need to changing equipment; Higher heat setting temperature makes the orientation texture disorientation of amorphous region accelerate simultaneously, and the internal stress of fiber is relaxed, and then improves the DIMENSIONAL STABILITY of fiber; The increase of setting temperature, the macromolecular chain mobility in fibre structure strengthens, and degree of crystallinity increases, and amorphous area content declines, and boiling water shrinkage reduces.
[accompanying drawing explanation]
Fig. 1 ageing-resistant preparation technology's schematic flow sheet of the present invention;
Fig. 2 ageing-resistant hydrogen nuclear magnetic resonance spectrogram of the present invention;
Fig. 3 ageing-resistant nuclear magnetic resonance of carbon spectrogram of the present invention;
The schematic diagram of Fig. 4 imitative triangle spinneret orifice of the present invention.
[detailed description of the invention]
The detailed description of the invention of a kind of colored profiled superfine denier polyester monofilament of the present invention and production method thereof is below provided.
Embodiment 1
A kind of colored profiled superfine denier polyester monofilament, its material quality percentage is:
The preparation method of described anti-aging capsule, its concrete steps are:
A () is to the preparation of dihydroxy Pyrogentisinic Acid base phosphine
With Phenylphosphine and paraformaldehyde for raw material, with water and isopropyl alcohol mixture for solvent, under catalyst action, affine addition reaction occurs, controlling reaction temperature is 35 ~ 50 DEG C, and the reaction time is 3 ~ 4h, prepare dihydroxymethyl phenyl phosphine, again at 85 ~ 95 DEG C, the mixed solution adding hydrogen peroxide and the concentrated sulfuric acid is strong oxidizer, oxidation 45 ~ 60min, prepare dihydroxymethyl phenyl phosphine oxide, by the hydroquinol base phosphine of synthesis, bromine water and iron powder add in reaction vessel, filter after being heated to 65 ~ 75 DEG C of reaction 0.5 ~ 1.75h and obtain kermesinus product, in the potassium hydroxide it being joined at normal temperatures 0.2mol/L and potassium ethoxide solution, in 80 ~ 95 DEG C of reaction 1 ~ 3h after dissolving completely, again product is recrystallized in steam bath, in triplicate, obtain white to dihydroxy Pyrogentisinic Acid base phosphine,
Described Phenylphosphine and the mol ratio of paraformaldehyde are 1: 2.2;
Catalyst is vanadic anhydride, and described Phenylphosphine and catalyst molar ratio value are 1: 0.035;
Described water and the volume ratio of isopropyl alcohol are 1: 0.95;
The mass fraction of described paraformaldehyde is 12%;
Described strong oxidizer and the mass values of Phenylphosphine are 1: 2.9;
The mass fraction of described hydrogen peroxide is 22%;
In described hydrogen peroxide and concentrated sulfuric acid solution, hydrogen peroxide and concentrated sulfuric acid volume ratio are 1: 2;
Described hydroquinol base phosphine, the mol ratio 1: 1.2: 0.01 of bromine water and iron powder;
Described potassium hydroxide and the mol ratio of potassium ethoxide are 1: 3.5;
The preparation of (b) ortho-nitraniline diazol
By ortho-nitraniline strong agitation be quickly cooled to 0 DEG C in the red fuming nitric acid (RFNA) of 12mol/L, after 1.5h, add the 4mol/L potassium nitrite aqueous solution, filter react 0.5 ~ 1.0h at 0 ~ 5 DEG C after, obtain ortho-nitraniline diazol;
The preparation of (c) azo-compound
That step (a) is prepared is added in the mixed solution of isopropyl alcohol and distilled water to dihydroxy Pyrogentisinic Acid base phosphine, keep solution temperature 5 ~ 10 DEG C, ortho-nitraniline diazol prepared by gradation instillation step (b), suction filtration, washing, dry azo-compound, it is rediance crystal;
Isopropyl alcohol in described isopropyl alcohol and the mixed solution of distilled water and the volume ratio of distilled water are 1: 0.75;
Described is 4% to dihydroxy Pyrogentisinic Acid base phosphine at the mass fraction of the mixed solution of isopropyl alcohol and distilled water;
Described is 1: 1 to the mol ratio of dihydroxy Pyrogentisinic Acid base phosphine and ortho-nitraniline diazol;
(d) ageing-resistant preparation
See Fig. 1, under nitrogen protection, azo-compound step (c) prepared joins in the water of the NaOH of 3.0mol/L and the mixed solution of ethanol, stir also gradation and add reductant thiourea dioxide, room temperature is cooled to react 2h at 60 ~ 65 DEG C after, add nitric acid pH to regulate between 5 ~ 6, suction filtration, dry in the shade, dry again after recrystallization, obtain functional modifier crude product, then by functional modifier crude product, hydrofluoric acid and red fuming nitric acid (RFNA) add in reaction vessel, after being heated to 65 ~ 75 DEG C of reaction 0.5 ~ 1.0h, filtration obtains Off-white product, through cooling suction filtration, dry in the shade, recrystallization and drying, obtain age resister,
Water in described water and the mixed solution of ethanol and the volume ratio of ethanol are 1: 1;
Described thiourea dioxide and the mol ratio of azo-compound are 1: 0.5;
Described functional modifier crude product, the mol ratio 1: 1.2: 0.01 of hydrofluoric acid and red fuming nitric acid (RFNA);
In fig. 2, the characteristic peak of amino (4.0ppm) is found no in the hydrogen nuclear magnetic resonance collection of illustrative plates of ageing-resistant molecule, after its generation nitrine coupling of corresponding ortho-nitraniline simultaneously, its molecular structure is symmetrical, therefore corresponding chemical shift (its unit is ppm) moves to (a and a ') 7.98ppm by original 7.94ppm and 6.72ppm, simultaneously 6.88ppm and 7.40ppm moves to (b and b ') 7.45ppm, and the hydrogen adjacent with phenolic hydroxy that on phenyl ring, 6.7ppm is corresponding is ripple hydrogen of living, be easy to the ortho-nitraniline generation coupling reaction of Azide, therefore corresponding chemical shift is that the number of hydrogen atoms of 6.7ppm reduces, existing chemical shift is (c and c ') 6.7ppm be the peak area ratio that (d) 7.1ppm is corresponding with chemical shift is 1: 2, namely a hydrogen atom is had to react, therefore illustrate that reaction is undertaken by design direction, its industry obtained is design and synthesis product.
In figure 3, for reaction monomers, to hydroxymethylphenol phosphine oxide, it only has five class carbon atoms, and due to the ortho-nitraniline generation coupling reaction with Azide, generate new carbon atom (d), its corresponding chemical shift moves to 131.0ppm by original 134.0ppm, simultaneously for (h) and (h ') carbon atom, it is symmetrical structure in reaction monomers, chemical shift is 116.0ppm, affect by adjacent nitrogen atom after there is coupling reaction, h () carbon atom cloud density increases it and moves to 115.8ppm by 116.0ppm, simultaneously corresponding (a) carbon atom is by adjacent (h) and (h ') carbon atom impact, chemical shift moves to 160.0ppm by 161.5ppm.Simultaneously for ortho-nitraniline, in reaction monomers, it is by six class carbon atoms, after Azide, coupling, reduction, its synthesis molecular structure of compounds is symmetrical, carbon atom kind in molecule is made to reduce to three classes, the carbon atom chemical shift of its correspondence by 119.7ppm and 135.7ppm move to (e ' and e) 127.4ppm, 121.9ppm and 117.2ppm moves to (g ' and g) 118.3ppm, 135.0ppm and 141.8ppm move to (b ' and b) 147.6ppm.Therefore ortho-nitraniline be described and chemical reaction be there occurs to hydroxymethylphenol phosphine oxide, and carrying out according to the direction of synthesis, obtaining required material.
The organic reagent of the group of the BTA of the application has the ageing resistace of excellent absorption living radical, age resister preparation technology synthesized by the present invention is simple, productive rate is high, and is easy to be separated, the raw material adopted in preparation process and solvent environmental protection; In age resister building-up process, adopt stable paraformaldehyde to be reaction raw materials, simultaneously paraformaldehyde is powder reagent, and be beneficial to transport and store, security is high, avoids the problems such as the Form aldehyde release that brings with formalin and solution transport difficult; Adopt the age resister with reactive end hydroxy functional group simultaneously, by the method for microcapsules, carry out coated with hydroxyethylcellulose, both ageing-resistant dispersiveness and stability had been improve, also achieve organic aging dose of dispersiveness in the material simultaneously, realize the ageing-resistant dispersed and high performance object of few additive; Simultaneously in age resister molecule because BTA functional group has excellent ageing resistace, especially because radiation makes material producing liveliness proof free radical, under ageing-resistant effect, make living radical inactivation, thus improve the ageing-resistant performance of material; The compatibility of hydroxyethylcellulose wall material and matrix material is better, is beneficial in modified microcapsule material fiber material and disperses, and affects few, on the basis ensureing fibre property, improve the ageing resistace of material to spinning and fibrous mechanical property;
The preparation of (e) anti-aging capsule
Take deionized water as solvent, age resister dispersion in a solvent, whipping temp is normal temperature, controlling whipping process medium-rate is 800 ~ 1200r/min, the dispersed with stirring time is 30 ~ 45min, age resister molecule is enable to form suspension system in aqueous, and then add hydroxyethylcellulose and dissolve, carry out high-speed stirred dispersion again, whipping temp is 45 ~ 55 DEG C, stir speed (S.S.) is 2000 ~ 3300r/min, mixing time is 20 ~ 30min, and then add BTCA carry out chitin be cross-linked, slaking 30min is carried out again under 65 ~ 80 DEG C of conditions, filtration obtains thick modification capsule, after carrying out vacuumize 24h at 60 DEG C again, obtain ageing-resistant anti-aging capsule, its sandwich layer is age resister, and cystoblast is hydroxyethylcellulose materials, and wherein, the Thickness Ratio of cystoblast and sandwich layer is 1: 15.
Described age resister addition is 4.5% relative to the mass fraction of water;
Described hydroxyethylcellulose addition is 2.7% relative to the mass fraction of water;
The weight average molecular weight of described hydroxyethylcellulose is 20000 ~ 25000, and molar substitution is 1.8 ~ 1.9.
Described BTCA is 0.45% relative to the mass fraction of chitin.
A production method for colored profiled superfine denier polyester monofilament, its concrete steps are:
Cut into slices by PEN, terylene chips, anti-aging capsule, pigment, dispersant, through the blended and melting of screw machine extruding, makes melt, carries out melt spinning through profile spinneret, obtain colored profiled superfine denier polyester monofilament.
Concrete technique is:
(1) cut into slices by PET, the section of blended preparation, through the blended granulation of screw rod, was heated at 8 ~ 12 hours to 120 ~ 160 DEG C and is dehydrated by PEN section, and insulation 8 ~ 10 hr aqueous amounts are at below 35PPM; Obtain mixed polyester section;
(2) pigment was heated at 8 ~ 12 hours to 120 ~ 160 DEG C and is carried out drying and dehydrating, and be incubated 8 ~ 10 hours, moisture is at below 35PPM;
(3) mixed polyester section and anti-aging capsule, pigment, dispersant, through the blended and melting of screw machine extruding, makes melt, spinning is carried out through spinnerets, temperature wherein through screw machine extruding is:: 270 ~ 280 DEG C, a district, two 275 ~ 285 DEG C, districts, three 280 ~ 290 DEG C, districts, four 280 ~ 295 DEG C, districts, five 275 ~ 290 DEG C, districts, six 275 ~ 290 DEG C, districts, screw pressure is 95 ~ 105kg/Cm2;
The shape of described spinnerets is selected from in-line, trilobal, triangle, the one in cross or five blade profiles.
See accompanying drawing 4, profile spinneret is triangle spinnerets, and its imitative triangle spinneret orifice is evenly distributed on triangle spinnerets, the cross sectional shape of imitative triangle spinneret orifice be equilateral triangle change circular arc into, circular arc is connected with leg-of-mutton both sides.
The number of degrees of described circular arc are 120 degree.
(4) strand that step (3) obtains is become spun filament fiber through lateral blowing cooled and solidified, lateral blowing temperature is 16 ~ 25 DEG C, and relative humidity is 80 ~ 90%;
(5) oil on the spun filament fiber solidified, finish weight concentration is 10 ~ 18%, and oil tanker rotating speed is 4 ~ 6 revs/min;
(6) spun filament fiber is after oiling, and batches shaping by up-coiler, and temperature is 24 ~ 28 DEG C, and relative humidity is 45 ~ 65%;
(7) the precursor bobbin batching shaping adopts stretching-machine to carry out heating secondary drawing, first step draft temperature is 125 ~ 135 DEG C, draw ratio is 3.5 ~ 4.5, second step draft temperature is 235 ~ 255 DEG C, and draw ratio is 1.2 ~ 1.5, and total stretching ratio is 4.2 ~ 6.75, heat setting temperature is 140 ~ 255 DEG C, lax ratio is 10% ~ 15%, and between stretching, temperature controls is 22 ~ 28 DEG C, and relative humidity is 55 ~ 75%; Examination of fibers after adding hot-stretch is classified as finished silk;
Every a branch of monofilament is 1 ~ 5, is preferably 1 ~ 3;
Filament number was 5 ~ 150 dawn, was preferably for 5 ~ 120 dawn;
This fiber single at 30 DEG C, single fiber 30 DEG C time, percentage elongation 15% ~ 35%, fracture strength is 2 ~ 8cN/dtex, and boiling water shrinkage is 1 ~ 5%; Colored non-conventional dimensionally stable polyester fiber, compared with identical fiber number circular fiber, described heterotypic fibre reaches same color can add the Masterbatch that mass ratio is 10 ~ 55% less.This fiber can be used for woven screen window and prepares the field of silk screen.
Embodiment 2
A kind of colored profiled superfine denier polyester monofilament, its material quality percentage is:
A kind of production method of colored profiled superfine denier polyester monofilament is with embodiment 1.
Embodiment 3
A kind of colored profiled superfine denier polyester monofilament, its material quality percentage is:
A kind of production method of colored profiled superfine denier polyester monofilament is with embodiment 1.
The above is only the preferred embodiment of the present invention; it should be pointed out that for those skilled in the art, without departing from the inventive concept of the premise; can also make some improvements and modifications, these improvements and modifications also should be considered within the scope of protection of the present invention.

Claims (10)

1. a colored profiled superfine denier polyester monofilament, is characterized in that, its material quality percentage is:
2. a kind of colored profiled superfine denier polyester monofilament as claimed in claim 1, is characterized in that, the mass percent of described anti-aging capsule is 3%.
3. a kind of colored profiled superfine denier polyester monofilament as claimed in claim 1, is characterized in that, the mass percent of described pigment is 7%.
4. a kind of colored profiled superfine denier polyester monofilament as claimed in claim 1, is characterized in that, the mass percent of described dispersant is 2%.
5. a kind of colored profiled superfine denier polyester monofilament as claimed in claim 1, it is characterized in that, described pigment is carbon black, AZO pigments, one or more in phthalocyanine color or Heterocyclics Pigments.
6. a kind of colored profiled superfine denier polyester monofilament as claimed in claim 1, it is characterized in that, the preparation method of described anti-aging capsule, its concrete steps are:
A () is to the preparation of dihydroxy Pyrogentisinic Acid base phosphine
The preparation of (b) ortho-nitraniline diazol
By ortho-nitraniline strong agitation be quickly cooled to 0 DEG C in the red fuming nitric acid (RFNA) of 12mol/L, after 1.5h, add the 4mol/L potassium nitrite aqueous solution, filter react 0.5 ~ 1.0h at 0 ~ 5 DEG C after, obtain ortho-nitraniline diazol;
The preparation of (c) azo-compound
That step (a) is prepared is added in the mixed solution of isopropyl alcohol and distilled water to dihydroxy Pyrogentisinic Acid base phosphine, keep solution temperature 5 ~ 10 DEG C, ortho-nitraniline diazol prepared by gradation instillation step (b), suction filtration, washing, dry azo-compound, it is rediance crystal;
Described is 4% to dihydroxy Pyrogentisinic Acid base phosphine at the mass fraction of the mixed solution of isopropyl alcohol and distilled water;
Described is 1 to the mol ratio of dihydroxy Pyrogentisinic Acid base phosphine and ortho-nitraniline diazol :1;
(d) ageing-resistant preparation
The preparation of (e) anti-aging capsule
Take deionized water as solvent, age resister dispersion in a solvent, whipping temp is normal temperature, controlling whipping process medium-rate is 800 ~ 1200r/min, the dispersed with stirring time is 30 ~ 45min, age resister molecule is enable to form suspension system in aqueous, and then add hydroxyethylcellulose and dissolve, carry out high-speed stirred dispersion again, whipping temp is 45 ~ 55 DEG C, stir speed (S.S.) is 2000 ~ 3300r/min, mixing time is 20 ~ 30min, and then add BTCA carry out chitin be cross-linked, slaking 30min is carried out again under 65 ~ 80 DEG C of conditions, filtration obtains thick modification capsule, after carrying out vacuumize 24h at 60 DEG C again, obtain containing ageing-resistant anti-aging capsule, its sandwich layer is age resister, and cystoblast is hydroxyethylcellulose materials, and wherein, the Thickness Ratio of cystoblast and sandwich layer is 1: 15.
Described age resister addition is 4.5% relative to the mass fraction of water;
Described hydroxyethylcellulose addition is 2.7% relative to the mass fraction of water;
Described BTCA is 0.45% relative to the mass fraction of chitin.
7. the production method of a kind of colored profiled superfine denier polyester monofilament as claimed in claim 1, it is characterized in that, its concrete steps are: cut into slices by PEN, terylene chips, anti-aging capsule, pigment, dispersant, melting after screw machine extruding is blended, makes melt, carry out melt spinning through profile spinneret, obtain colored profiled superfine denier polyester monofilament.
8. the production method of a kind of colored profiled superfine denier polyester monofilament as claimed in claim 7, it is characterized in that, the shape of described spinnerets is selected from in-line, trilobal, triangle, the one in cross or five blade profiles.
9. the production method of a kind of colored profiled superfine denier polyester monofilament as claimed in claim 8, it is characterized in that, profile spinneret is triangle spinnerets, its imitative triangle spinneret orifice is evenly distributed on triangle spinnerets, the cross sectional shape of imitative triangle spinneret orifice be equilateral triangle while change circular arc into, circular arc is connected with leg-of-mutton both sides.
10. the production method of a kind of colored profiled superfine denier polyester monofilament as claimed in claim 9, is characterized in that, the number of degrees of described circular arc are 120 degree.
CN201510685136.5A 2015-10-20 2015-10-20 Colored special-shaped super fine denier polyester monofilaments and production method thereof Pending CN105297169A (en)

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