CN106283259B - Porous imitative hair polyester fiber of one kind and preparation method thereof - Google Patents

Porous imitative hair polyester fiber of one kind and preparation method thereof Download PDF

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Publication number
CN106283259B
CN106283259B CN201610781179.8A CN201610781179A CN106283259B CN 106283259 B CN106283259 B CN 106283259B CN 201610781179 A CN201610781179 A CN 201610781179A CN 106283259 B CN106283259 B CN 106283259B
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tpa
terephthalic acid
modified poly
poly ester
spinneret
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CN106283259A (en
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王彦芳
王丽丽
李文刚
王建根
史宁
张烨
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Jiangsu Hengli Chemical Fiber Co Ltd
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Jiangsu Hengli Chemical Fiber Co Ltd
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    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/92—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/181—Acids containing aromatic rings
    • C08G63/183—Terephthalic acids
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/08—Melt spinning methods
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/24—Formation of filaments, threads, or the like with a hollow structure; Spinnerette packs therefor
    • D01D5/247—Discontinuous hollow structure or microporous structure
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/253—Formation of filaments, threads, or the like with a non-circular cross section; Spinnerette packs therefor
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/10—Other agents for modifying properties

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Artificial Filaments (AREA)

Abstract

The present invention relates to a kind of porous imitative hair polyester fibers and preparation method thereof, and porous imitative hair polyester fiber is made using porous spinneret spinning in modified poly ester；The arrangement mode of spinneret orifice is oval shaped arrangements on porous spinneret, i.e. the hole center of spinneret orifice is located on concentration ellipse, and concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.Porous imitative hair polyester fiber is made by the FDY processing of modified poly ester POY and modified poly ester, and the preparation method of modified poly ester is：Ethylene glycol terephthalate is made with glycol reaction in terephthalic acid (TPA), and terephthalic acid (TPA) is added and reacts terephthalic acid (TPA) binary alcohol esters obtained with the propylene glycol containing branch, the reaction was continued obtains modified poly ester.Fibre property produced by the present invention is excellent, line density deviation ratio≤2.0%, fracture strength CV value≤4.0%, extension at break CV value≤8.0%, crimp contraction coefficient of variation CV value≤8.0%.

Description

Porous imitative hair polyester fiber of one kind and preparation method thereof
Technical field
The invention belongs to field of polyester fiber, are related to porous imitative hair polyester fiber of one kind and preparation method thereof.
Background technology
Polyethylene terephthalate (PET fiber or polyester fiber) fiber since the advent of the world, have fracture strength and Elasticity modulus is high, and resilience is moderate, and thermal finalization is excellent, and heat-resisting light resistance is good and acid-fast alkali-proof corrosion resistance etc. is a series of excellent Performance, and fabric has many advantages, such as wash and wear, stiffness is good, is widely used in the fields such as clothes, home textile.
But due to the crystallinity of PET height, compact structure, and the functional group not being combined with dyestuff on strand cause Dye molecule hardly enters fibrous inside, and dyeing is difficult.People be cannot be satisfied to bright-coloured beautiful, unique style fabric demand.
The reason for causing PET dyeing difficult is the straight chain macromolecular that PET belongs to symmetry, and strand does not contain side chain radical Group, regularity is very good, its main chain contains rigid phenyl ring and alkyl flexible, and the ester group being directly connected with phenyl ring with Phenyl ring constitutes rigid conjugated system again, to constrain rotating freely for its soft segment.Such a structure increases molecules The wall ridge of sub-chain motion, causes the glass transition temperature of PET higher, needs to promote dye molecule under very high temperature condition Staining procedure is completed in diffusion to fibrous inside.In addition, the strand of PET is regular, good crystallinity, strand arrangement is close, and And the polar group not having an effect with dye molecule on strand, keep the colouring of PET fiber more difficult.
Therefore, under the general high temperature and pressure of the dyeing of common PET fiber, disperse dyeing is selected, when temperature reaches PET When fiber obtains glass transition temperature or more, gap increases between PET fiber polymer molecule, but the increased degree of its free volume is small, Dyeing rate is not high, but it is the main problem faced now that energy consumption and dye-uptake caused by high temperature and high pressure method are low.In addition, PET fiber melt viscosity is higher, is unfavorable for processing.
There are many method for preparing PET fiber, and wherein melt spinning method is one kind more in current industrial production application.It is molten Melt many of spinning process parameter, these parameters determine the course of fiberizing and spin the structure and performance of fiber, production Upper is exactly the fiber for being made by controlling these parameters required performance.The main spinning that can will be controlled in production according to technical process Silk summary of parameters.An is melting condition, spinning conditions, condition of cure, wrapping wire condition etc., and wherein strand cools and solidifies condition to fiber Structure has conclusive influence with performance, and the cooling velocity and its uniformity of polyester fondant thread, are generally adopted in production in order to control Take cooling blowing.Cooling blowing can accelerate the cooling velocity of melt stream, be conducive to improve spinning speed；Reinforce empty around strand The convection current of gas keeps the cooling of ectonexine strand uniform, to create condition using porous spinneret；Cooling blowing can make as-spun fibre Quality advance, tensile property improve, and are conducive to the production capacity for improving equipment.
Experimental branch line all uses cross air blasting as the type of cooling for a long time, and energy consumption accounts for long filament production cost very Most of, as people increasingly improve chemical fibre performance and quality requirements, the exploitation of chemical-fibres filaments new product is to high added value Fibre in differentiation direction is developed, it is desirable that higher cooling blowing condition then proposes ring blowing device.Ring blowing device is not only Have a uniform advantage of every synnema wind-engaging, and energy consumption is compared to relatively low, effective solution cross air blasting since blowing area is big and Caused by wind energy lose problem.
In spinning process, although ring blowing has apparent advantage, problem is still remained：Due to spun silk from After round spinneret squeezes out, by ring wind quenching, since the round spinneret number of turns is more so that ring blowing hardly enters most interior Layer, leads to that the silk of innermost layer may be also uncolled after cooling in outermost silk, so that fiber number occur irregular for the silk of gained, The problems such as intensity is irregular, uneven dyeing causes the further processing subsequently to silk difficulty occur.
Wool-Like abnormal contraction composite filament is the long filament with different potential shrinkages, i.e. high-shrinkage filament POY and lower shrinkage Composite filaments of the silk FDY through mixed fine processing composition, the main feature of the different contraction mixed fiber composite silks of PET：High loft and soft hand Sense.PET Wool-Like abnormal contraction composite filaments it is outer existing similar with common long filament.It is thermally treated due to the difference of two component shrinking percentages Afterwards, high convergency part forms clear-cut core filaments, becomes the skeleton of silk, and lower shrinkage part forms tiny wire ring and is wound on core filaments Around, it is exactly like textured filament in appearance.Gloss is soft.Due to bulk and surface many of PET Wool-Like abnormal contraction composite filaments Wire ring eliminates the aurora defect of chemical fibre silk fabrics.Excellent warmth retention property.The high loft of the different contraction mixed fiber composite silks of PET increases Gap between big fiber.The air content in the different contraction mixed fiber composite silk fabrics of PET is caused to increase.
Invention content
The purpose of the present invention is overcoming the problems such as existing dyeing polyester fibers are irregular, mechanical property is poor, realize extensive The production spinning of change provides porous imitative hair polyester fiber of one kind and preparation method thereof.The raw material of the polyester fiber of the present invention is to change Property polyester, the propylene glycol segment containing branch, porous imitative hair polyester prepared by modified polyester are introduced in the strand of modified poly ester Fiber, under the conditions of certain temperature, the increasing degree of the spatial joint clearance of porous imitative hair polyester fiber interior molecules interchain is far longer than Unbranched conventional polyester fiber at same temperature, is conducive to the molecules such as coloring agent and enters internal degree, improve dyeing Rate；The melt viscosity of porous imitative hair polyester fiber reduces, and reduces processing temperature, reduces degradation rate, is conducive to process；In addition The destruction not big to the structural regularity of porous imitative hair polyester fiber of propylene glycol segment containing branch, maintains polyester fiber Excellent performance.The spinneret that spinneret orifice oval shaped arrangements are used in spinning process of the present invention, is conducive to fiber in spinning process It is uniform, be fully cooled, performance between fiber and structure difference are smaller, improve the dyeing uniformity and mechanical property of fiber Energy.
In order to achieve the above objectives, the technical solution adopted by the present invention is：
The material of a kind of porous imitative hair polyester fiber, the porous imitative hair polyester fiber is modified poly ester, and the modification is poly- Ester is made of terephthalic acid (TPA) segment, ethylene glycol segment and propylene glycol segment containing branch, the propylene glycol segment containing branch Refer on a non-end group carbon that branch is located in propylene glycol segment and branch is the linear carbon chain containing 5-10 carbon atom Propylene glycol segment；
The fiber number of the porous imitative hair polyester fiber is 150-300dtex, initial modulus≤85cN/dtex, fracture strength >=2.1cN/dtex, elongation at break be 15.0 ± 2.0%, crimp contraction be 5.50 ± 3.0%, internet pricing be 90 ± 5/ m；The porous imitative hair polyester fiber in the case where temperature is 80~130 DEG C, the spatial joint clearance of fibrous inside molecule interchain increases 10~ 30v/v%；Line density deviation ratio≤2.0% of the porous imitative hair polyester fiber, fracture strength CV value≤4.0%, fracture are stretched Long CV value≤8.0%, crimp contraction coefficient of variation CV value≤8.0%, boiling water shrinkage are 5.0 ± 1.0%.
The present invention also provides a kind of preparation methods of porous imitative hair polyester fiber, and modified poly ester is used porous spinneret Porous imitative hair polyester fiber is made in spinning；The arrangement mode of spinneret orifice is oval shaped arrangements on the porous spinneret, described ellipse Circular arrangement refers to that the hole center of spinneret orifice is located on concentration ellipse, and the concentration ellipse is that series is oval, all elliptical length Axis is conllinear, and short axle is conllinear；
The preparation method of the porous imitative hair polyester fiber is：By modified poly ester through metering, extrusion, cooling, oil and roll up Around obtained modified poly ester POY；By Modified polyester chips through metering, extrusion, cooling, oil, stretch, thermal finalization and winding, system Obtain modified poly ester FDY；Then by modified poly ester POY and modified poly ester FDY through combining network, heating stretching, false twisting, heat Sizing and coiling and molding；
The preparation process of the modified poly ester is：
(1) preparation of terephthalic acid (TPA) binary alcohol esters；
After terephthalic acid (TPA) and the propylene glycol containing branch are made into slurry, under the catalytic action of the concentrated sulfuric acid, it is esterified Terephthalic acid (TPA) binary alcohol esters are obtained by the reaction；The propylene glycol containing branch refers to that be located in propylene glycol segment one of branch is non- On end group carbon and branch be the linear carbon chain containing 5-10 carbon atom propylene glycol；
For the propylene glycol containing branch, branch is alkyl, is electron-withdrawing group, in the presence of branch, makes strand Spatial volume increases, and solvation becomes smaller, and proton is not easy to dissociate in dihydric alcohol so that the propylene glycol containing branch and terephthaldehyde The reactivity of acid is less than ethylene glycol, mixes according to same ethylene glycol and reacts with terephthalic acid (TPA), can cause the third two containing branch Alcohol reaction is imperfect, to influence ratio of the propylene glycol containing branch in polyester macromolecule, and then influences the performance of polyester.This Using the propylene glycol containing branch is first carried out esterification under the catalytic action of sulfuric acid with terephthalic acid (TPA), product exists for invention It is added after ethylene glycol and p phthalic acid esterification, ensure that the stability of the propylene glycol proportioning containing branch；
(2) preparation of ethylene glycol terephthalate；
After terephthalic acid (TPA) and ethylene glycol are made into slurry, esterification is carried out, ethylene glycol terephthalate is obtained；
(3) preparation of modified poly ester；
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, stir Mix mixing, under the action of catalyst and stabilizer, under conditions of negative pressure, successively carry out low vacuum stage polycondensation reaction and Modified poly ester is made in the polycondensation reaction of high vacuum stage of Fig.
As preferred technical solution：
A kind of preparation method of porous imitative hair polyester fiber as described above, the specific preparation process of the modified poly ester For：
(1) preparation of terephthalic acid (TPA) binary alcohol esters；
Terephthalic acid (TPA) and the propylene glycol containing branch are made into slurry, under the catalytic action of the concentrated sulfuric acid, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure is normal pressure~0.3MPa, and temperature is 180~240 DEG C, works as ester It is esterification terminal to change when the water quantity of distillate in reaction reaches 90% of theoretical value or more, obtains terephthalic acid (TPA) dihydric alcohol Ester；
(2) preparation of ethylene glycol terephthalate；
After terephthalic acid (TPA) and ethylene glycol are made into slurry, esterification is carried out, esterification is pressurizeed in nitrogen atmosphere Reaction, moulding pressure are normal pressure~0.3MPa, and temperature is 250~260 DEG C, when the water quantity of distillate in esterification reaches theoretical value 90% or more when be esterification terminal, obtain ethylene glycol terephthalate；
(3) preparation of modified poly ester；
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, stir Mixing 15-20 minutes is mixed, under the action of catalyst and stabilizer, the polycondensation for starting low vacuum stage under conditions of negative pressure is anti- It answers, which by normal pressure is steadily evacuated to absolute pressure 500Pa hereinafter, temperature control is at 260~270 DEG C, and the reaction time is 30~50 minutes；It then proceedes to vacuumize, carries out the polycondensation reaction of high vacuum stage of Fig, so that reaction pressure is down to absolute pressure and be less than Modified poly ester is made in 275~280 DEG C, 50~90 minutes reaction time in 100Pa, reaction temperature control；
Described modified poly ester POY main spinning technology parameters are：
Spinning temperature：280-290℃；
Cooling temperature：18-22℃；
Winding speed：3200-3600m/min；
Described modified poly ester FDY main spinning technology parameters are：
Spinning temperature：280-290℃；
Cooling temperature：20-25℃；
Network pressure：0.20-0.30MPa；
One roller speed：2200-2600m/min；
One roll temperature：75-85℃；
Two roller speeds：3650-3850m/min；
Two roll temperatures：115-135℃；
Winding speed：3600-3800m/min；
The main spinning technology parameter of the porous imitative hair polyester fiber is：
Spin speed：400-800m/min；
Sizing over feed rate(OFR)：3.5-5.50%；
Wind over feed rate(OFR)：2.5-5.0%；
T1：180-220℃；
T2：150-180℃；
DR：1.6-1.8；
D/Y:1.6-2.0；
Network pressure：0.05-0.3MPa.
A kind of preparation method of porous imitative hair polyester fiber as described above, in step (1), terephthalic acid (TPA) with contain branch Propylene glycol molar ratio be 1:1.3-1.5；Concentrated sulfuric acid addition is the 0.3-0.5% of terephthalic acid (TPA) weight；The dense sulphur A concentration of 50-60wt% of acid；
In step (2), the molar ratio of terephthalic acid (TPA) and ethylene glycol is 1:1.2~2.0；
In step (3), the Mole percent ratio of the terephthalic acid (TPA) binary alcohol esters and ethylene glycol terephthalate is 2 ~5%；The catalyst is antimony oxide, antimony glycol or antimony acetate, and catalyst charge is terephthalic acid (TPA) total weight 0.01%~0.05%；The stabilizer is triphenyl phosphate, trimethyl phosphate or Trimethyl phosphite, stabilizer addition It is the 0.01%~0.05% of the terephthalic acid (TPA) total weight；
The number-average molecular weight of the modified poly ester is 15000~30000.
A kind of preparation method of porous imitative hair polyester fiber as described above, the propylene glycol containing branch are 2- amyls- 1,3 propylene glycol, -1,3 propylene glycol of 2- hexyls, -1,3 propylene glycol of 2- heptyl, -1,3 propylene glycol of 2- octyls, -1,3 propylene glycol of 2- nonyls Or one or more of -1,3 propylene glycol of 2- decyls.
A kind of preparation method of porous imitative hair polyester fiber as described above, the spinneret orifice be arranged as long axis and/or Short axle is symmetrical.
The ratio of a kind of preparation method of porous imitative hair polyester fiber as described above, elliptical long axis and minor axis length is 1.3~1.8；The guide hole diameter that the spacing of adjacent spinneret orifice is more than or equal to spinneret orifice adds 1.5mm.When the effective area of spinneret Mutually simultaneously as the perimeter of ellipse is more than circular perimeter, the number of plies of spinneret orifice oval shaped arrangements is less than the layer of circular arrangement Number, the hole count of spinneret orifice oval shaped arrangements are more than the hole count of circular arrangement, and therefore, spinneret orifice oval shaped arrangements are conducive to ring blowing Cooling, improve the cooling efficiency of ring blowing, the fibre property of preparation is also more excellent.Long axis and the ratio of minor axis length more connect It is bordering on 1, ellipse is more similar to justify, and the difference of cooling efficiency and cooling effect is little；Long axis and the ratio of minor axis length are 1.3 When, cooling effect significantly improves, and individual pen hole count accordingly increases by 16%；When long axis and the ratio of minor axis length are 1.8, cooling effect Improve larger, individual pen hole count accordingly increases by 33%, in the case of identical hole count, and oval shaped arrangements of the invention are justified than conventional concentric arranges The number of turns of row is reduced, and is easy to cooling wind and is blown through, makes the fiber cooling condition of Internal and external cycle evenly；The ratio of long axis and minor axis length When more than 1.8, ellipse is partial to form flat shape, is not easy to punch, cooling no longer increases.Therefore, series is ellipse The ratio of round long axis and minor axis length is 1.3~1.8, can reach higher cooling efficiency and preferable cooling effect.
A kind of preparation method of porous imitative hair polyester fiber as described above, the spinneret are round spinneret or ellipse Shape spinneret；The diameter of the circle spinneret and the difference of the oval maximum long axis length of series are more than 10mm, the ellipse Shape spinneret and the difference of the oval maximum long axis length of series are more than 10mm.
A kind of preparation method of porous imitative hair polyester fiber as described above, the guide hole a diameter of 1.5 of the spinneret orifice~ 2.5mm；The spinneret hole count of the spinneret is more than or equal to 192.
A kind of preparation method of porous imitative hair polyester fiber as described above, the cross section of the spinneret orifice of the spinneret Shape is circle, square, diamond shape, "-" type, triangular form, trilobal cross, hollow type or platypelloid type.
The principle of the present invention is：
For unbranched polyester fiber, molecular chain structure is the linear macromolecule containing benzene ring structure, on strand Functional group's marshalling, regularity is good, flexible poor；Its free volume increments is small when the temperature rises, the resistance of these characteristics Dyestuff has been hindered to enter inside polyester fiber, thus dyeability is poor.
The raw material of the polyester fiber of the present invention is modified poly ester, the propylene glycol containing branch contained in modified poly ester macromolecular Segment, when temperature is higher than glass transition temperature, branch makes the increasing degree of free volume be far longer than no branch prior to backbone motion The characteristic of the polyester macromolecule chain of chain, the increase of free volume improves molecule and enters degree inside polyester, modified The free volume of polyester fiber prepared by polyester is far longer than polyester fiber unbranched at same temperature, increases the diffusion of dyestuff Degree improves the dyeability of polyester fiber.Meanwhile polyester fiber prepared by modified poly ester advantageously reduces melt viscosity, has Conducive to its processing performance of improvement.The introducing of propylene glycol segment containing the branch destruction not big to polyester fiber structures regularity, Maintain the excellent performance of polyester fiber.
When the effective area phase of spinneret is simultaneously as the perimeter of ellipse is more than circular perimeter, spinneret orifice ellipse The number of plies of arrangement is less than the number of plies of circular arrangement, and the hole count of spinneret orifice oval shaped arrangements is more than the hole count of circular arrangement, using spray The spinneret of wire hole oval shaped arrangements enables to fiber quick, uniformly cooling, and the difference of structure and performance is smaller between fiber, Be conducive to improve the performance of the even dyeing rate and fiber of fiber.
Advantageous effect：
1) arrangement mode of spinneret orifice is oval shaped arrangements on spinneret of the invention, and the effective area of spinneret is identical When, the number of plies of spinneret orifice oval shaped arrangements is less than the number of plies of circular arrangement, and ring blowing is easier to blow through dynamic analysis of spinning, dynamic analysis of spinning Cooling effect it is more preferable, the fibre property of preparation is also more excellent.
2) arrangement mode of spinneret orifice is oval shaped arrangements on spinneret of the invention, and the effective area of spinneret is identical When, the hole count of spinneret orifice oval shaped arrangements is more than the hole count of circular arrangement, and oval shaped arrangements can realize a greater degree of cooling, Significantly improve cooling efficiency.
3) material of porous imitative hair polyester fiber produced by the present invention is modified poly ester, is contained in modified poly ester macromolecular Propylene glycol segment containing branch, when temperature is higher than glass transition temperature, branch makes the increase width of free volume prior to backbone motion Degree is far longer than the characteristic of unbranched polyester macromolecule chain, and the increase of free volume improves molecule and enters inside polyester Degree, the free volume of polyester fiber is increased to increase the diffusion of dyestuff by branch, improves the dye of polyester fiber Color performance.
4) porous imitative hair polyester fiber produced by the present invention, the increase of polyester fiber free volume advantageously reduce melt and glue Degree, is conducive to improve its processing performance.
5) porous imitative hair polyester fiber produced by the present invention, the polyester fiber of the introducing pair of the propylene glycol segment containing branch The not big destruction of structural regularity, maintains the excellent performance of polyester fiber.
6) porous imitative hair dyeing polyester fibers performance and good mechanical performance produced by the present invention, initial modulus≤85cN/ Dtex, line density deviation ratio≤2.0% of porous imitative hair polyester fiber, fracture strength CV value≤4.0%, extension at break CV values≤ 8.0%, crimp contraction coefficient of variation CV value≤8.0%.
Description of the drawings
Fig. 1 is the oval shaped arrangements figure of 374 spinneret orifices, and the aperture of spinneret orifice is 2.0mm, the length of transverse and short axle It is 1.3 to spend ratio；
Fig. 2 is the circular arrangement figure of 370 spinneret orifices, and the aperture of spinneret orifice is 2.0mm；
Fig. 3 is the oval shaped arrangements figure of 382 spinneret orifices, and the aperture of spinneret orifice is 2.0mm, the length of transverse and short axle It is 1.6 to spend ratio.
Specific implementation mode
The invention will be further elucidated with reference to specific embodiments.It should be understood that these embodiments are merely to illustrate this hair It is bright rather than limit the scope of the invention.In addition, it should also be understood that, after reading the content taught by the present invention, art technology Personnel can make various changes or modifications the present invention, and such equivalent forms equally fall within the application the appended claims and limited Fixed range.Embodiment 1
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.3 terephthalic acid (TPA) is made into slurry with 2- amyl -1,3 propylene glycol and is added in reactor, A concentration of 50wt%, addition are to carry out esterification under the catalytic action of 0.3% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure are normal pressure, and temperature is 180 DEG C, when the water in esterification distillates Amount is esterification terminal when reaching the 90% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.2 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure are normal pressure, and temperature is 250 DEG C, when the water in esterification distillates Amount is esterification terminal when reaching the 90% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 2%, is stirred 15 minutes, is being added Amount is 0.01% the catalytic antimony trioxide of terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight 0.01% Stabilizer triphenyl phosphate under the action of, under conditions of negative pressure start low vacuum stage polycondensation reaction, the staged pressure It is 500Pa that absolute pressure is steadily evacuated to by normal pressure, and at 260 DEG C, the reaction time is 30 minutes for temperature control；It then proceedes to take out true Sky carries out the polycondensation reaction of high vacuum stage of Fig, and it is 100Pa so that reaction pressure is down to absolute pressure, and reaction temperature is controlled 275 DEG C, modified poly ester was made in 50 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 15000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- penta Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- amyl -1,3 propylene glycol segments and ethylene glycol segment is 2%.
Table 1：Embodiment 2-12 important technological parameters
Embodiment 2
The preparation process of the modified poly ester of embodiment 2 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 16 minutes, is terephthalic acid (TPA) total weight in addition 0.011% the catalytic antimony trioxide and addition is 0.02% stabilizer triphenyl phosphate of terephthalic acid (TPA) total weight Under the action of, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolutely by normal pressure Pressure 490Pa, at 262 DEG C, the reaction time is 31 minutes for temperature control；It then proceedes to vacuumize, carries out the contracting of high vacuum stage of Fig Poly- reaction, makes reaction pressure be down to absolute pressure 90Pa, and reaction temperature control is made and is modified in 276 DEG C, 51 minutes reaction time Polyester.
The number-average molecular weight of modified poly ester be 16000, modified poly ester by terephthalic acid (TPA) segment, ethylene glycol segment and 2- oneself Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- hexyl -1,3 propylene glycol segments and ethylene glycol segment is 2.1%.
Embodiment 3
The preparation process of the modified poly ester of embodiment 3 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 16 minutes, in 0.03% that addition is terephthalic acid (TPA) total weight The catalytic antimony trioxide and addition be terephthalic acid (TPA) total weight 0.02% stabilizer triphenyl phosphate effect Under, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolute pressure by normal pressure 498Pa, at 263 DEG C, the reaction time is 32 minutes for temperature control；It then proceedes to vacuumize, the polycondensation for carrying out high vacuum stage of Fig is anti- It answers, reaction pressure is made to be down to absolute pressure 90Pa, reaction temperature control is made modified poly- in 277 DEG C, 57 minutes reaction time Ester.
The number-average molecular weight of modified poly ester is 15900, and modified poly ester is by terephthalic acid (TPA) segment, ethylene glycol segment and 2- heptan Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- heptyl -1,3 propylene glycol segments and ethylene glycol segment is 2.2%.
Embodiment 4
The preparation process of the modified poly ester of embodiment 4 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 17 minutes, is terephthalic acid (TPA) total weight in addition 0.033% the catalytic antimony trioxide and addition is 0.023% stabilizer phosphoric acid triphen of terephthalic acid (TPA) total weight Under the action of ester, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolutely by normal pressure It is 497Pa to pressure, at 264 DEG C, the reaction time is 33 minutes for temperature control；It then proceedes to vacuumize, carries out high vacuum stage of Fig Polycondensation reaction, it is 80Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is at 278 DEG C, 58 minutes reaction time, system Obtain modified poly ester.
The number-average molecular weight of modified poly ester is 15800, and modified poly ester is pungent by terephthalic acid (TPA) segment, ethylene glycol segment and 2- Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- octyl -1,3 propylene glycol segments and ethylene glycol segment is 2.3%.
Embodiment 5
The preparation process of the modified poly ester of embodiment 5 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 17 minutes, is terephthalic acid (TPA) total weight in addition 0.034% the catalytic antimony trioxide and addition is 0.024% stabilizer phosphoric acid triphen of terephthalic acid (TPA) total weight Under the action of ester, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolutely by normal pressure To pressure 496Pa, at 265 DEG C, the reaction time is 34 minutes for temperature control；It then proceedes to vacuumize, carries out high vacuum stage of Fig Polycondensation reaction, it is 80Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made in 277 DEG C, 59 minutes reaction time Modified poly ester.
The number-average molecular weight of modified poly ester is 15900, and modified poly ester is by terephthalic acid (TPA) segment, ethylene glycol segment and 2- nonyls Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- nonyl -1,3 propylene glycol segments and ethylene glycol segment is 2.4%.
Embodiment 6
The preparation process of the modified poly ester of embodiment 6 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 18 minutes, is terephthalic acid (TPA) total weight in addition 0.035% the catalytic antimony trioxide and addition is 0.025% stabilizer phosphoric acid triphen of terephthalic acid (TPA) total weight Under the action of ester, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolutely by normal pressure To pressure 495Pa, at 266 DEG C, the reaction time is 35 minutes for temperature control；It then proceedes to vacuumize, carries out high vacuum stage of Fig Polycondensation reaction, it is 70Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made in 278 DEG C, 60 minutes reaction time Modified poly ester.
The number-average molecular weight of modified poly ester is 16000, and modified poly ester is by terephthalic acid (TPA) segment, ethylene glycol segment and the 2- last of the ten Heavenly stems Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- decyl -1,3 propylene glycol segments and ethylene glycol segment is 2.5%.
Embodiment 7
The preparation process of the modified poly ester of embodiment 7 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 19 minutes, is terephthalic acid (TPA) total weight in addition 0.036% the catalytic antimony trioxide and addition is 0.025% stabilizer phosphoric acid triphen of terephthalic acid (TPA) total weight Under the action of ester, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolutely by normal pressure To pressure 496Pa, at 267 DEG C, the reaction time is 36 minutes for temperature control；It then proceedes to vacuumize, carries out high vacuum stage of Fig Polycondensation reaction, it is 70Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made in 278 DEG C, 61 minutes reaction time Modified poly ester.
The number-average molecular weight of modified poly ester is 16000, and the number-average molecular weight of modified poly ester is 16000, and modified poly ester is by right Phthalic acid segment, ethylene glycol segment and 2- amyl -1,3 propylene glycol segments composition, 2- amyl -1,3 propylene glycol segments and second two The Mole percent ratio of alcohol segment is 2.6%.
Embodiment 8
The preparation process of the modified poly ester of embodiment 8 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 19 minutes, is terephthalic acid (TPA) total weight in addition 0.036% the catalytic antimony trioxide and addition is 0.025% stabilizer phosphoric acid triphen of terephthalic acid (TPA) total weight Under the action of ester, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolutely by normal pressure To pressure 496Pa, at 267 DEG C, the reaction time is 36 minutes for temperature control；It then proceedes to vacuumize, carries out high vacuum stage of Fig Polycondensation reaction, it is 70Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made in 278 DEG C, 61 minutes reaction time Modified poly ester.
The number-average molecular weight of modified poly ester be 17000, modified poly ester by terephthalic acid (TPA) segment, ethylene glycol segment and 2- oneself Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- hexyl -1,3 propylene glycol segments and ethylene glycol segment is 2.7%.
Embodiment 9
The preparation process of the modified poly ester of embodiment 9 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 16 minutes, in 0.04% that addition is terephthalic acid (TPA) total weight Catalyst glycol antimony and addition be terephthalic acid (TPA) total weight 0.026% stabilizer trimethyl phosphate effect Under, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolute pressure by normal pressure 497Pa, at 268 DEG C, the reaction time is 38 minutes for temperature control；It then proceedes to vacuumize, the polycondensation for carrying out high vacuum stage of Fig is anti- It answers, it is 60Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made modified poly- in 279 DEG C, 62 minutes reaction time Ester.
The number-average molecular weight of modified poly ester is 17000, and modified poly ester is by terephthalic acid (TPA) segment, ethylene glycol segment and 2- heptan Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- heptyl -1,3 propylene glycol segments and ethylene glycol segment is 2.8%.
Embodiment 10
The modified poly ester preparation process of embodiment 10 is with embodiment 1, wherein main technical parameter is referring to table 1；In step (3) it after terephthalic acid (TPA) binary alcohol esters being added, is stirred 17 minutes, in 0.03% that addition is terephthalic acid (TPA) total weight Catalyst glycol antimony and addition be terephthalic acid (TPA) total weight 0.027% stabilizer trimethyl phosphate effect Under, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolute pressure by normal pressure 498Pa, at 269 DEG C, the reaction time is 39 minutes for temperature control；It then proceedes to vacuumize, the polycondensation for carrying out high vacuum stage of Fig is anti- It answers, it is 60Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made modified poly- in 278 DEG C, 64 minutes reaction time Ester.
The number-average molecular weight of modified poly ester is 17000, and modified poly ester is pungent by terephthalic acid (TPA) segment, ethylene glycol segment and 2- Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- octyl -1,3 propylene glycol segments and ethylene glycol segment is 3%.
Embodiment 11
The preparation process of the modified poly ester of embodiment 11 is with embodiment 1, wherein main technical parameter is referring to table 1；In step Suddenly it after terephthalic acid (TPA) binary alcohol esters are added in (3), is stirred 18 minutes, is terephthalic acid (TPA) total weight in addition 0.04% catalyst glycol antimony and addition is 0.03% stabilizer trimethyl phosphate of terephthalic acid (TPA) total weight Under effect, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolute pressure by normal pressure Power 497Pa, at 260 DEG C, the reaction time is 40 minutes for temperature control；It then proceedes to vacuumize, carries out the polycondensation of high vacuum stage of Fig Reaction, it is 60Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made and is modified in 277 DEG C, 63 minutes reaction time Polyester.
The number-average molecular weight of modified poly ester is 18000, and modified poly ester is by terephthalic acid (TPA) segment, ethylene glycol segment and 2- nonyls Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- nonyl -1,3 propylene glycol segments and ethylene glycol segment is 4%.
Embodiment 12
The preparation process of the modified poly ester of embodiment 12 is with embodiment 1, wherein main technical parameter is referring to table 1；In step Suddenly it after terephthalic acid (TPA) binary alcohol esters are added in (3), is stirred 18 minutes, is terephthalic acid (TPA) weight in addition 0.038% catalyst acetic acid antimony and addition is the work of 0.03% stabilizer Trimethyl phosphite of terephthalic acid (TPA) weight Under, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, which is steadily evacuated to absolute pressure by normal pressure 497Pa, at 265 DEG C, the reaction time is 42 minutes for temperature control；It then proceedes to vacuumize, the polycondensation for carrying out high vacuum stage of Fig is anti- It answers, it is 40Pa so that reaction pressure is down to absolute pressure, and reaction temperature control is made modified poly- in 277 DEG C, 70 minutes reaction time Ester.
The number-average molecular weight of modified poly ester obtained is 26000, by terephthalic acid (TPA) segment, ethylene glycol segment and the 2- last of the ten Heavenly stems Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- decyl -1,3 propylene glycol segments and ethylene glycol segment is 4%.
Embodiment 13
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.5 terephthalic acid (TPA) is made into slurry with 2- decyl -1,3 propylene glycol and is added in reactor, A concentration of 60wt%, addition are to carry out esterification under the catalytic action of 0.5% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.3MPa, temperature is 240 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:2.0 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.3MPa, temperature is 260 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 5%, is stirred 20 minutes, is being added Amount be 0.05% catalyst acetic acid antimony of terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight 0.05% it is steady Under the action of determining agent Trimethyl phosphite, under conditions of negative pressure start low vacuum stage polycondensation reaction, the staged pressure by It is 450Pa that normal pressure, which is steadily evacuated to absolute pressure, and at 270 DEG C, the reaction time is 50 minutes for temperature control；It then proceedes to vacuumize, The polycondensation reaction for carrying out high vacuum stage of Fig, it is 30Pa so that reaction pressure is down to absolute pressure, and reaction temperature is controlled at 280 DEG C, instead 90 minutes between seasonable, modified poly ester is made.
The number-average molecular weight of modified poly ester obtained is 30000, by terephthalic acid (TPA) segment, ethylene glycol segment and the 2- last of the ten Heavenly stems Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- decyl -1,3 propylene glycol segments and ethylene glycol segment is 5%.
Embodiment 14
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.47 terephthalic acid (TPA) is made into slurry with 2- nonyl -1,3 propylene glycol and is added in reactor, A concentration of 60wt%, addition are to carry out esterification under the catalytic action of 0.47% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 220 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.8 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 258 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4%, is stirred 18 minutes, is being added Amount is 0.04% catalyst glycol antimony of terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight 0.04% Under the action of stabilizer trimethyl phosphate, under conditions of negative pressure start low vacuum stage polycondensation reaction, the staged pressure by Normal pressure is steadily evacuated to absolute pressure 460Pa, and at 263 DEG C, the reaction time is 47 minutes for temperature control；It then proceedes to vacuumize, into The polycondensation reaction of row high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40Pa, and reaction temperature is controlled at 278 DEG C, reaction Between 85 minutes, be made modified poly ester.
The number-average molecular weight of modified poly ester obtained is 28000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- nonyls Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- nonyl -1,3 propylene glycol segments and ethylene glycol segment is 4%.
Embodiment 15
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.46 terephthalic acid (TPA) is made into slurry with 2- octyl -1,3 propylene glycol and is added in reactor, A concentration of 60wt%, addition are to carry out esterification under the catalytic action of 0.49% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 233 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.8 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 259 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.5%, is stirred 19 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.044% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.046% stabilizer triphenyl phosphate, start the polycondensation reaction of low vacuum stage, the rank under conditions of negative pressure Section pressure is steadily evacuated to absolute pressure 490Pa by normal pressure, and at 269 DEG C, the reaction time is 48 minutes for temperature control；It then proceedes to take out Vacuum carries out the polycondensation reaction of high vacuum stage of Fig, and reaction pressure is made to be down to absolute pressure 40Pa, and reaction temperature is controlled at 279 DEG C, Modified poly ester was made in 87 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 29000, pungent by terephthalic acid (TPA) segment, ethylene glycol segment and 2- Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- octyl -1,3 propylene glycol segments and ethylene glycol segment is 4.5%.
Embodiment 16
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.49 terephthalic acid (TPA) is made into slurry with 2- heptyl -1,3 propylene glycol and is added in reactor, A concentration of 60wt%, addition are to carry out esterification under the catalytic action of 0.48% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 230 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.8 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 258 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.7%, is stirred 19 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.048% catalyst glycol antimony that amount is terephthalic acid (TPA) weight and addition Under the action of 0.047% stabilizer triphenyl phosphate, start the polycondensation reaction of low vacuum stage, the rank under conditions of negative pressure Section pressure is steadily evacuated to absolute pressure 460Pa by normal pressure, and at 267 DEG C, the reaction time is 48 minutes for temperature control；It then proceedes to take out Vacuum carries out the polycondensation reaction of high vacuum stage of Fig, and reaction pressure is made to be down to absolute pressure 40Pa, and reaction temperature is controlled at 279 DEG C, Modified poly ester was made in 83 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 27000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- heptan Base -1,6 hexylene glycol segment forms, and the Mole percent ratio of 2- heptyl -1,6 hexylene glycol segments and ethylene glycol segment is 4.7%.
Embodiment 17
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.467 terephthalic acid (TPA) is made into slurry with 2- hexyl -1,3 propylene glycol and is added in reactor, In a concentration of 60wt%, addition is be esterified anti-under the catalytic action of 0.47% concentrated sulfuric acid of terephthalic acid (TPA) weight It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 236 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.89 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 258 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.3%, is stirred 18 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.04% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.041% stabilizer Trimethyl phosphite, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, it should Staged pressure is steadily evacuated to absolute pressure 490Pa by normal pressure, and at 268 DEG C, the reaction time is 48 minutes for temperature control；It then proceedes to It vacuumizes, carries out the polycondensation reaction of high vacuum stage of Fig, reaction pressure is made to be down to absolute pressure 40Pa, reaction temperature is controlled 278 DEG C, modified poly ester was made in 85 minutes reaction time.
The number-average molecular weight of modified poly ester obtained be 29000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- oneself Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- hexyl -1,3 propylene glycol segments and ethylene glycol segment is 4.3%.
Embodiment 18
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.48 terephthalic acid (TPA) is made into slurry with 2- amyl -1,3 propylene glycol and is added in reactor, A concentration of 55wt%, addition are to carry out esterification under the catalytic action of 0.46% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 230 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.88 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 256 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.7%, is stirred 18 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.047% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.047% stabilizer triphenyl phosphate, start the polycondensation reaction of low vacuum stage, the rank under conditions of negative pressure Section pressure is steadily evacuated to absolute pressure 480Pa by normal pressure, and at 265 DEG C, the reaction time is 47 minutes for temperature control；It then proceedes to take out Vacuum carries out the polycondensation reaction of high vacuum stage of Fig, and reaction pressure is made to be down to absolute pressure 40Pa, and reaction temperature is controlled at 279 DEG C, Modified poly ester was made in 85 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 28000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- penta Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- amyl -1,3 propylene glycol segments and ethylene glycol segment is 4.7%.
Embodiment 19
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.46 terephthalic acid (TPA) is made into slurry with 2- decyl -1,3 propylene glycol and is added in reactor, A concentration of 55wt%, addition are to carry out esterification under the catalytic action of 0.47% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 238 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.9 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 259 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching 92% of theoretical value or more, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.7%, is stirred 19 minutes, is adding Enter the 0.046% catalyst acetic acid antimony that amount is terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight 0.048% Stabilizer Trimethyl phosphite under the action of, under conditions of negative pressure start low vacuum stage polycondensation reaction, the stage pressure It is 446Pa that power, which is steadily evacuated to absolute pressure by normal pressure, and at 267 DEG C, the reaction time is 49 minutes for temperature control；It then proceedes to take out true Sky carries out the polycondensation reaction of high vacuum stage of Fig, and it is 40Pa so that reaction pressure is down to absolute pressure, and reaction temperature is controlled at 278 DEG C, Modified poly ester was made in 87 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 29000, by terephthalic acid (TPA) segment, ethylene glycol segment and the 2- last of the ten Heavenly stems Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- decyl -1,3 propylene glycol segments and ethylene glycol segment is 4.7%.
Embodiment 20
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.46 terephthalic acid (TPA) is made into slurry with 2- nonyl -1,3 propylene glycol and is added in reactor, A concentration of 60wt%, addition are to carry out esterification under the catalytic action of 0.46% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.26MPa, temperature is 221 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.89 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.25MPa, temperature is 259 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.1%, is stirred 18 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.041% catalyst glycol antimony that amount is terephthalic acid (TPA) weight and addition Under the action of 0.042% stabilizer trimethyl phosphate, start the polycondensation reaction of low vacuum stage, the rank under conditions of negative pressure Section pressure is steadily evacuated to absolute pressure 460Pa by normal pressure, and at 265 DEG C, the reaction time is 47 minutes for temperature control；It then proceedes to take out Vacuum carries out the polycondensation reaction of high vacuum stage of Fig, and reaction pressure is made to be down to absolute pressure 40Pa, and reaction temperature is controlled at 278 DEG C, Modified poly ester was made in 85 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 28000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- nonyls Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- nonyl -1,3 propylene glycol segments and ethylene glycol segment is 4.1%.
Embodiment 21
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.43 terephthalic acid (TPA) is made into slurry with 2- octyl -1,3 propylene glycol and is added in reactor, A concentration of 60wt%, addition are to carry out esterification under the catalytic action of 0.47% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 235 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.78 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.26MPa, temperature is 255 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.3%, is stirred 17 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.043% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.049% stabilizer triphenyl phosphate, start the polycondensation reaction of low vacuum stage, the rank under conditions of negative pressure Section pressure is steadily evacuated to absolute pressure 490Pa by normal pressure, and at 268 DEG C, the reaction time is 46 minutes for temperature control；It then proceedes to take out Vacuum carries out the polycondensation reaction of high vacuum stage of Fig, and reaction pressure is made to be down to absolute pressure 40Pa, and reaction temperature is controlled at 275 DEG C, Modified poly ester was made in 85 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 28000, pungent by terephthalic acid (TPA) segment, ethylene glycol segment and 2- Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- octyl -1,3 propylene glycol segments and ethylene glycol segment is 4.3%.
Embodiment 22
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.43 terephthalic acid (TPA) is made into slurry with 2- heptyl -1,3 propylene glycol and is added in reactor, A concentration of 55wt%, addition are to carry out esterification under the catalytic action of 0.45% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.29MPa, temperature is 235 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.87 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 255 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.6%, is stirred 18 minutes, is adding Enter 0.047% catalyst glycol antimony that amount is terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight 0.04% Stabilizer triphenyl phosphate under the action of, under conditions of negative pressure start low vacuum stage polycondensation reaction, the staged pressure Absolute pressure 470Pa is steadily evacuated to by normal pressure, at 268 DEG C, the reaction time is 45 minutes for temperature control；It then proceedes to vacuumize, The polycondensation reaction for carrying out high vacuum stage of Fig makes reaction pressure be down to absolute pressure 40Pa, and reaction temperature is controlled at 279 DEG C, reaction Modified poly ester was made in 83 minutes time.
The number-average molecular weight of modified poly ester obtained is 29000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- heptan Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- heptyl -1,3 propylene glycol segments and ethylene glycol segment is 4.6%.
Embodiment 23
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.457 terephthalic acid (TPA) is made into slurry with 2- hexyl -1,3 propylene glycol and is added in reactor, A concentration of 55%, addition is to carry out esterification under the catalytic action of 0.46% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 239 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.81 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 255 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.41%, is stirred 19 minutes, Addition is 0.042% the catalytic antimony trioxide of terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight Under the action of 0.048% stabilizer Trimethyl phosphite, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, it should Staged pressure is steadily evacuated to absolute pressure 495Pa by normal pressure, and at 265 DEG C, the reaction time is 45 minutes for temperature control；It then proceedes to It vacuumizes, carries out the polycondensation reaction of high vacuum stage of Fig, reaction pressure is made to be down to absolute pressure 50Pa, reaction temperature is controlled 275 DEG C, modified poly ester was made in 85 minutes reaction time.
The number-average molecular weight of modified poly ester obtained be 28000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- oneself Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- hexyl -1,3 propylene glycol segments and ethylene glycol segment is 4.41%.
Embodiment 24
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.47 terephthalic acid (TPA) is made into slurry with 2- amyl -1,3 propylene glycol and is added in reactor, A concentration of 55wt%, addition are to carry out esterification under the catalytic action of 0.48% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 245 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.81 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 259 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.67%, is stirred 19 minutes, Addition is 0.041% the catalytic antimony trioxide of terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight Under the action of 0.042% stabilizer triphenyl phosphate, start the polycondensation reaction of low vacuum stage, the rank under conditions of negative pressure Section pressure is steadily evacuated to absolute pressure 485Pa by normal pressure, and at 268 DEG C, the reaction time is 46 minutes for temperature control；It then proceedes to take out Vacuum carries out the polycondensation reaction of high vacuum stage of Fig, and reaction pressure is made to be down to absolute pressure 50Pa, and reaction temperature is controlled at 275 DEG C, Modified poly ester was made in 89 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 29000, by terephthalic acid (TPA) segment, ethylene glycol segment and 2- penta Base -1,3 propylene glycol segment forms, and the Mole percent ratio of 2- amyl -1,3 propylene glycol segments and ethylene glycol segment is 4.67%.
Embodiment 25
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.45 terephthalic acid (TPA) is mixed with -1,3 propylene glycol of -1,3 propylene glycol of 2- hexyls and 2- amyls It closes object to be made into slurry addition reactor, wherein the molar ratio of 2- hexyls -1,3 propylene glycol and 2- amyl -1,3 propylene glycol is 3:1, A concentration of 55%, addition is to carry out esterification under the catalytic action of 0.49% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.26MPa, temperature is 236 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.8 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 258 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.4%, is stirred 18 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.042% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.047% stabilizer Trimethyl phosphite, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, it should Staged pressure is steadily evacuated to absolute pressure 495Pa by normal pressure, and at 265 DEG C, the reaction time is 49 minutes for temperature control；It then proceedes to It vacuumizes, carries out the polycondensation reaction of high vacuum stage of Fig, reaction pressure is made to be down to absolute pressure 50Pa, reaction temperature is controlled 278 DEG C, modified poly ester was made in 88 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 29000, by terephthalic acid (TPA) segment, ethylene glycol segment, 2- hexyls- 1,3 propylene glycol segment and 2- amyl -1,3 propylene glycol segments composition, 2- hexyl -1,3 propylene glycol segments and 2- amyls -1,3 the third two The summation of alcohol segment is 4.4% with the Mole percent ratio of ethylene glycol segment.
Embodiment 26
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.45 terephthalic acid (TPA) and -1,3 propylene glycol of 2- octyls and -1,3 propylene glycol of 2- amyls Mixture is made into slurry and is added in reactor, and the molar ratio of wherein 2- octyls -1,3 propylene glycol and 2- amyl -1,3 propylene glycol is 3: 2, a concentration of 60%, addition is be esterified anti-under the catalytic action of 0.45% concentrated sulfuric acid of terephthalic acid (TPA) weight It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 239 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.84 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, be esterified anti- It answers, esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.29MPa, temperature is 255 DEG C, when in esterification Water quantity of distillate is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.6%, is stirred 18 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.0423% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.045% stabilizer Trimethyl phosphite, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, it should Staged pressure is steadily evacuated to absolute pressure 495Pa by normal pressure, and at 265 DEG C, the reaction time is 45 minutes for temperature control；It then proceedes to It vacuumizes, carries out the polycondensation reaction of high vacuum stage of Fig, reaction pressure is made to be down to absolute pressure 50Pa, reaction temperature is controlled 278 DEG C, modified poly ester was made in 85 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 28000, by terephthalic acid (TPA) segment, ethylene glycol segment, 2- octyls- 1,3 propylene glycol segment and 2- amyl -1,3 propylene glycol segments composition, 2- octyl -1,3 propylene glycol segments and 2- amyls -1,3 the third two The Mole percent ratio of alcohol segment and ethylene glycol segment is 4.6%.
Embodiment 27
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.45 terephthalic acid (TPA) is mixed with -1,3 propylene glycol of -1,3 propylene glycol of 2- hexyls and 2- amyls It closes object to be made into slurry addition reactor, wherein the molar ratio of 2- hexyls -1,3 propylene glycol and 2- amyl -1,3 propylene glycol is 3:1, A concentration of 55%, addition is to carry out esterification under the catalytic action of 0.49% concentrated sulfuric acid of terephthalic acid (TPA) weight, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.26MPa, temperature is 236 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 96% of theoretical value, obtains terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.8 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.28MPa, temperature is 258 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.4%, is stirred 18 minutes, is adding It is terephthalic acid (TPA) weight to enter 0.042% the catalytic antimony trioxide that amount is terephthalic acid (TPA) weight and addition Under the action of 0.047% stabilizer Trimethyl phosphite, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, it should Staged pressure is steadily evacuated to absolute pressure 495Pa by normal pressure, and at 265 DEG C, the reaction time is 49 minutes for temperature control；It then proceedes to It vacuumizes, carries out the polycondensation reaction of high vacuum stage of Fig, reaction pressure is made to be down to absolute pressure 50Pa, reaction temperature is controlled 278 DEG C, modified poly ester was made in 88 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 29000, by terephthalic acid (TPA) segment, ethylene glycol segment, 2- hexyls- 1,3 propylene glycol segment and 2- amyl -1,3 propylene glycol segments composition, 2- hexyl -1,3 propylene glycol segments and 2- amyls -1,3 the third two The summation of alcohol segment is 4.4% with the Mole percent ratio of ethylene glycol segment.
Embodiment 28
A kind of preparation method of modified poly ester, specifically includes following steps：
(1) preparation of terephthalic acid (TPA) binary alcohol esters：
It is 1 by molar ratio:1.45 terephthalic acid (TPA) and -1,3 propylene glycol of 2- octyls, -1,3 propylene glycol of 2- amyls and 2- oneself The mixture of base -1,3 propylene glycol is made into slurry and is added in reactor, wherein 2- octyls -1,3 propylene glycol, 2- amyls -1,3 the third two The molar ratio of -1,3 propylene glycol of alcohol and 2- hexyls is 3:2:1, a concentration of 60%, addition is terephthalic acid (TPA) weight Under the catalytic action of 0.47% concentrated sulfuric acid, esterification, esterification compressive reaction in nitrogen atmosphere, moulding pressure are carried out For 0.29MPa, temperature is 235 DEG C, is esterification terminal when the water quantity of distillate in esterification reaches the 92% of theoretical value, Obtain terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate：
It is 1 by molar ratio:1.8 terephthalic acid (TPA)s and ethylene glycol are added after being made into slurry in reactor, carry out esterification, Esterification compressive reaction in nitrogen atmosphere, moulding pressure 0.27MPa, temperature is 258 DEG C, when the water in esterification evaporates Output is esterification terminal when reaching the 92% of theoretical value, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester：
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, it is right The Mole percent ratio of phthalic acid binary alcohol esters and ethylene glycol terephthalate is 4.71%, is stirred 18 minutes, Addition is 0.04% the catalytic antimony trioxide of terephthalic acid (TPA) weight and addition is terephthalic acid (TPA) weight Under the action of 0.041% stabilizer Trimethyl phosphite, start the polycondensation reaction of low vacuum stage under conditions of negative pressure, it should Staged pressure is steadily evacuated to absolute pressure 490Pa by normal pressure, and at 268 DEG C, the reaction time is 49 minutes for temperature control；It then proceedes to It vacuumizes, carries out the polycondensation reaction of high vacuum stage of Fig, reaction pressure is made to be down to absolute pressure 50Pa, reaction temperature is controlled 277 DEG C, modified poly ester was made in 84 minutes reaction time.
The number-average molecular weight of modified poly ester obtained is 29000, by terephthalic acid (TPA) segment, ethylene glycol segment, band branch Glycol segment composition, wherein branched glycol segment be 2- octyl -1,3 propylene glycol segment, 2- amyl -1,3 propylene glycol chains Section and 2- hexyl -1,3 propylene glycol segments composition, the Mole percent ratio of branched glycol segment and ethylene glycol segment are 4.71%.
Embodiment 29
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
As shown in Figure 1, elliptical long axis and the ratio of minor axis length are 1.3, the spacing of adjacent spinneret orifice is equal to spinneret orifice Guide hole diameter add 1.5mm, spinneret is round spinneret, diameter and the oval maximum long axial length of series of round spinneret The difference of degree is 11mm, and the spinneret hole count of a diameter of 2.0mm of guide hole of spinneret orifice, spinneret are 374, the spinneret orifice of spinneret Cross-sectional shape be circle.
By modified poly ester made from embodiment 1 through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, The spinning temperature that modified poly ester is POY is 285 DEG C, and cooling temperature is 18 DEG C, winding speed 3200m/min；By modified poly ester Slice through metering, extrusion, cooling, oil, stretch, thermal finalization and winding, modified poly ester FDY is made, modified poly ester FDY Spinning temperature is 285 DEG C, and cooling temperature is 25 DEG C, network pressure 0.25MPa, and a roller speed is 2400m/min, a roll temperature It it is 80 DEG C, two roller speeds are 3800m/min, and two roll temperatures are 120 DEG C, winding speed 3750m/min；Then by modified poly ester Porous imitative hair polyester is made through combining network, heating stretching, false twisting, thermal finalization and coiling and molding in POY and modified poly ester FDY The spinning speed of fiber, porous imitative hair polyester fiber is 600m/min, and sizing over feed rate(OFR) is 4.50%, and winding over feed rate(OFR) is 4.0%, T1 It it is 200 DEG C, T2 is 180 DEG C, DR 1.7, D/Y 1.8, network pressure 0.15MPa.
The fiber number of porous imitative hair polyester fiber obtained is 240tex, initial modulus 83cN/dtex, and fracture strength is 4.7cN/dtex, elongation at break 15.7%, crimp contraction 4.53%, internet pricing are 90/m；Porous imitative hair polyester For fiber in the case where temperature is 80 DEG C, the spatial joint clearance of fibrous inside molecule interchain increases 15v/v%；The line of porous imitative hair polyester fiber Density variation rate is 1.7%, and fracture strength CV values are 3.2%, and extension at break CV values are 6.9%, the crimp contraction coefficient of variation CV values are 7.2%, boiling water shrinkage 5.5%.
Embodiment 30
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
As shown in figure 3, elliptical long axis and the ratio of minor axis length are 1.6, the spacing of adjacent spinneret orifice is equal to spinneret orifice Guide hole diameter add 1.5mm, spinneret is round spinneret, diameter and the oval maximum long axial length of series of round spinneret The difference of degree is 11mm, and the spinneret hole count of a diameter of 2.0mm of guide hole of spinneret orifice, spinneret are 382, the spinneret orifice of spinneret Cross-sectional shape be circle.
By modified poly ester made from embodiment 1 through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, The spinning temperature that modified poly ester is POY is 285 DEG C, and cooling temperature is 18 DEG C, winding speed 3200m/min；By modified poly ester Slice through metering, extrusion, cooling, oil, stretch, thermal finalization and winding, modified poly ester FDY is made, modified poly ester FDY Spinning temperature is 285 DEG C, and cooling temperature is 25 DEG C, network pressure 0.25MPa, and a roller speed is 2400m/min, a roll temperature It it is 80 DEG C, two roller speeds are 3800m/min, and two roll temperatures are 120 DEG C, winding speed 3750m/min；Then by modified poly ester Porous imitative hair polyester is made through combining network, heating stretching, false twisting, thermal finalization and coiling and molding in POY and modified poly ester FDY The spinning speed of fiber, porous imitative hair polyester fiber is 600m/min, and sizing over feed rate(OFR) is 4.50%, and winding over feed rate(OFR) is 4.0%, T1 It it is 200 DEG C, T2 is 180 DEG C, DR 1.7, D/Y 1.8, network pressure 0.15MPa.
The fiber number of porous imitative hair polyester fiber obtained is 270dtex, initial modulus 85cN/dtex, and fracture strength is 5.2cN/dtex, elongation at break 16.6%, crimp contraction 4.77%, internet pricing are 95/m；Porous imitative hair polyester For fiber in the case where temperature is 80 DEG C, the spatial joint clearance of fibrous inside molecule interchain increases 15v/v%；The line of porous imitative hair polyester fiber Density variation rate is 1.2%, and fracture strength CV values are 3.1%, and extension at break CV values are 5.3%, the crimp contraction coefficient of variation CV values are 4.9%, boiling water shrinkage 5.7%.
Comparative example 1
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is circular arrangement on filament plate, and circular arrangement refers to that the hole center of spinneret orifice is located on concentric circles, with one heart Circle is round for series.As shown in Fig. 2, the guide hole diameter that the spacing of adjacent spinneret orifice is equal to spinneret orifice adds 1.5mm, spinneret is The difference of round spinneret, the diameter and the round maximum diameter of series of round spinneret is 11mm, the guide hole diameter of spinneret orifice Spinneret hole count for 2.0mm, spinneret is 370, and the cross-sectional shape of the spinneret orifice of spinneret is circle.
By modified poly ester made from embodiment 1 through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, The spinning temperature that modified poly ester is POY is 285 DEG C, and cooling temperature is 18 DEG C, winding speed 3200m/min；By modified poly ester Slice through metering, extrusion, cooling, oil, stretch, thermal finalization and winding, modified poly ester FDY is made, modified poly ester FDY Spinning temperature is 285 DEG C, and cooling temperature is 25 DEG C, network pressure 0.25MPa, and a roller speed is 2400m/min, a roll temperature It it is 80 DEG C, two roller speeds are 3800m/min, and two roll temperatures are 120 DEG C, winding speed 3750m/min；Then by modified poly ester Porous imitative hair polyester is made through combining network, heating stretching, false twisting, thermal finalization and coiling and molding in POY and modified poly ester FDY The spinning speed of fiber, porous imitative hair polyester fiber is 600m/min, and sizing over feed rate(OFR) is 4.50%, and winding over feed rate(OFR) is 4.0%, T1 It it is 200 DEG C, T2 is 180 DEG C, DR 1.7, D/Y 1.8, network pressure 0.15MPa.
The fiber number of porous imitative hair polyester fiber obtained is 143dtex, initial modulus 87cN/dtex, and fracture strength is 1.7cN/dtex, elongation at break 12.1%, crimp contraction 2.6%, internet pricing are 91/m；Porous imitative hair polyester is fine For dimension in the case where temperature is 80 DEG C, the spatial joint clearance of fibrous inside molecule interchain increases 15v/v%；The line of porous imitative hair polyester fiber is close It is 2.6% to spend deviation ratio, and fracture strength CV values are 4.5%, and extension at break CV values are 8.2%, crimp contraction coefficient of variation CV Value is 8.5%, boiling water shrinkage 3.1%.
With embodiment 29 comparison as can be seen that the effective area of spinneret it is identical when, (circular arrangement when spinneret hole count is close Spinneret hole count is 370, and oval shaped arrangements spinneret hole count is that 374), the spinneret orifice number of plies of oval shaped arrangements is 6, is less than circular arrangement The spinneret orifice number of plies 8, cooling effect is more preferable；It is oval with the comparison of embodiment 30 as can be seen that when the identical effective area of spinneret The spinneret orifice number of plies of shape arrangement is 5, is less than the spinneret orifice number of plies 8 of circular arrangement, cooling effect is more preferable, the spinneret of oval shaped arrangements The hole count 382 in hole is more than the hole count 370 of the spinneret orifice of circular arrangement, cooling efficiency higher.The comparing result of fibre property shows Fiber linear density deviation ratio made from embodiment 29 and embodiment 30, fracture strength CV values, extension at break CV values and evenness fault Rate CV values are less than comparative example 1, under the conditions of illustrating same process, fibroid made from the spinneret using spinneret orifice oval shaped arrangements It can be better than the spinneret using spinneret circular arrangement.
Embodiment 31~33
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice is arranged as long axial symmetry, and the ratio of elliptical long axis and minor axis length is 1.4, between adjacent spinneret orifice 1.6mm is added away from the guide hole diameter equal to spinneret orifice, spinneret is round spinneret, and the diameter and series of round spinneret are oval The difference of maximum long axis length is 12mm, a diameter of 1.5mm of guide hole of spinneret orifice, the spinneret orifice numerical digit 192 of spinneret, spinneret The cross-sectional shape of the spinneret orifice of plate is square.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 280 DEG C, and cooling temperature is 18 DEG C, winding speed 3200m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 280 DEG C, Cooling temperature is 20 DEG C, network pressure 0.20MPa, and a roller speed is 2200m/min, and a roll temperature is 75 DEG C, two roller speeds For 3650m/min, two roll temperatures are 115 DEG C, winding speed 3600m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 400m/min, and sizing over feed rate(OFR) is 3.50%, and it is 180 DEG C that winding over feed rate(OFR), which is 2.5%, T1, T2 180 DEG C, DR 1.6, D/Y 1.6, network pressure 0.05MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 5.2-5.9, the mechanical performance data such as following table of the spatial joint clearance Magnification of fibrous inside molecule interchain and fiber at 80 DEG C.
Embodiment 34~36
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice is arranged as that short axle is symmetrical, and the ratio of elliptical long axis and minor axis length is 1.4, between adjacent spinneret orifice 1.7mm is added away from the guide hole diameter equal to spinneret orifice, spinneret is elliptical spinneret plate, and elliptical spinneret plate is oval most with series The difference of big long axis length is 12mm, and the spinneret hole count of a diameter of 1.8mm of guide hole of spinneret orifice, spinneret are 200, spinneret Spinneret orifice cross-sectional shape be diamond shape.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 282 DEG C, and cooling temperature is 22 DEG C, winding speed 3250m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 281 DEG C, Cooling temperature is 21 DEG C, network pressure 0.30MPa, and a roller speed is 2250m/min, and a roll temperature is 77 DEG C, two roller speeds For 3680m/min, two roll temperatures are 116 DEG C, winding speed 3630m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 450m/min, and sizing over feed rate(OFR) is 3.9%, and it is 180 DEG C that winding over feed rate(OFR), which is 2.9%, T1, T2 150 DEG C, DR 1.6, D/Y 1.6, network pressure 0.30MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 4.0-4.9, the mechanical performance data such as following table of the spatial joint clearance Magnification of fibrous inside molecule interchain and fiber at 90 DEG C.
Embodiment 37~39
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice be arranged as long axis and short axle is symmetrical, the ratio of elliptical long axis and minor axis length is 1.4, adjacent spinneret The guide hole diameter that the spacing in hole is equal to spinneret orifice adds 1.8mm, and spinneret is round spinneret, the diameter of round spinneret be The difference of the oval maximum long axis length of row is 13mm, a diameter of 2.5mm of guide hole of spinneret orifice, and the spinneret hole count of spinneret is 200, the cross-sectional shape of the spinneret orifice of spinneret is "-" type.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 283 DEG C, and cooling temperature is 20 DEG C, winding speed 3400m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 284 DEG C, Cooling temperature is 23 DEG C, network pressure 0.25MPa, and a roller speed is 2300m/min, and a roll temperature is 78 DEG C, two roller speeds For 3700m/min, two roll temperatures are 125 DEG C, winding speed 3650m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 470m/min, and sizing over feed rate(OFR) is 4.50%, and it is 220 DEG C that winding over feed rate(OFR), which is 3.5%, T1, T2 150 DEG C, DR 1.6, D/Y 1.7, network pressure 0.17MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 4.2-4.9, the spatial joint clearance Magnification of fibrous inside molecule interchain and the mechanical performance data of fiber are as follows at 100 DEG C Table.
Embodiment 40~42
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice be arranged as long axis and short axle is symmetrical, the ratio of elliptical long axis and minor axis length is 1.7, adjacent spinneret The guide hole diameter that the spacing in hole is equal to spinneret orifice adds 1.9mm, and spinneret is elliptical spinneret plate, elliptical spinneret plate and series The difference of oval maximum long axis length is 14mm, and the spinneret hole count of a diameter of 1.5mm of guide hole of spinneret orifice, spinneret are 210, The cross-sectional shape of the spinneret orifice of spinneret is triangular form.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 283 DEG C, and cooling temperature is 19 DEG C, winding speed 3300m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 284 DEG C, Cooling temperature is 20 DEG C, network pressure 0.23MPa, and a roller speed is 2500m/min, and a roll temperature is 79 DEG C, two roller speeds For 3800m/min, two roll temperatures are 124 DEG C, winding speed 3750m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 600m/min, and sizing over feed rate(OFR) is 4.70%, and it is 185 DEG C that winding over feed rate(OFR), which is 5.0%, T1, T2 170 DEG C, DR 1.7, D/Y 1.8, network pressure 0.18MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 5.2-6.0, the spatial joint clearance Magnification of fibrous inside molecule interchain and the mechanical performance data of fiber are as follows at 110 DEG C Table.
Embodiment 43~45
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice is arranged as that short axle is symmetrical, and the ratio of elliptical long axis and minor axis length is 1.8, between adjacent spinneret orifice 1.5mm is added away from the guide hole diameter equal to spinneret orifice, spinneret is round spinneret, and the diameter and series of round spinneret are oval The difference of maximum long axis length is 15mm, and the spinneret hole count of a diameter of 1.8mm of guide hole of spinneret orifice, spinneret are 240, spinneret The cross-sectional shape of the spinneret orifice of plate is trilobal cross.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 290 DEG C, and cooling temperature is 20 DEG C, winding speed 3450m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 290 DEG C, Cooling temperature is 23 DEG C, network pressure 0.23MPa, and a roller speed is 2450m/min, and a roll temperature is 76 DEG C, two roller speeds For 3790m/min, two roll temperatures are 125 DEG C, winding speed 3740m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 560m/min, and sizing over feed rate(OFR) is 5.50%, and it is 190 DEG C that winding over feed rate(OFR), which is 3.5%, T1, T2 170 DEG C, DR 1.7, D/Y 1.7, network pressure 0.19MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 5.2-5.7, the spatial joint clearance Magnification of fibrous inside molecule interchain and the mechanical performance data of fiber are as follows at 120 DEG C Table.
Embodiment 46~49
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice is arranged as long axial symmetry, and the ratio of elliptical long axis and minor axis length is 1.8, between adjacent spinneret orifice 1.6mm is added away from the guide hole diameter equal to spinneret orifice, spinneret is round spinneret, and the diameter and series of round spinneret are oval The difference of maximum long axis length is 16mm, and the spinneret hole count of a diameter of 2.2mm of guide hole of spinneret orifice, spinneret are 250, spinneret The cross-sectional shape of the spinneret orifice of plate is hollow type.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 288 DEG C, and cooling temperature is 21 DEG C, winding speed 3470m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 284 DEG C, Cooling temperature is 23 DEG C, network pressure 0.240MPa, and a roller speed is 2600m/min, and a roll temperature is 79 DEG C, two roller speeds For 3780m/min, two roll temperatures are 124 DEG C, winding speed 3730m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 800m/min, and sizing over feed rate(OFR) is 4.3%, and it is 190 DEG C that winding over feed rate(OFR), which is 4.1%, T1, T2 163 DEG C, DR 1.7, D/Y 1.8, network pressure 0.24MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 4.7-5.4, the spatial joint clearance Magnification of fibrous inside molecule interchain and the mechanical performance data of fiber are as follows at 130 DEG C Table.
Embodiment 50~53
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice is arranged as that short axle is symmetrical, and the ratio of elliptical long axis and minor axis length is 1.8, between adjacent spinneret orifice 1.8mm is added away from the guide hole diameter equal to spinneret orifice, spinneret is round spinneret, and the diameter and series of round spinneret are oval The difference of maximum long axis length is 15mm, and the spinneret hole count of a diameter of 2.5mm of guide hole of spinneret orifice, spinneret are 260, spinneret The cross-sectional shape of the spinneret orifice of plate is platypelloid type.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 286 DEG C, and cooling temperature is 21 DEG C, winding speed 3600m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 282 DEG C, Cooling temperature is 22 DEG C, network pressure 0.23MPa, and a roller speed is 2460m/min, and a roll temperature is 85 DEG C, two roller speeds For 3850m/min, two roll temperatures are 135 DEG C, winding speed 3800m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 630m/min, and sizing over feed rate(OFR) is 4.1%, and it is 180 DEG C that winding over feed rate(OFR), which is 4.6%, T1, T2 150 DEG C, DR 1.8, D/Y 2.0, network pressure 0.21MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 4.2-5.1, the spatial joint clearance Magnification of fibrous inside molecule interchain and the mechanical performance data of fiber are as follows at 100 DEG C Table.
Embodiment 54~57
A kind of preparation method of porous imitative hair polyester fiber, porous imitative hair polyester fiber are made using porous spinneret, spray The arrangement mode of spinneret orifice is oval shaped arrangements on filament plate, and oval shaped arrangements refer to that the hole center of spinneret orifice is located at concentration ellipse On, concentration ellipse is that series is oval, and all elliptical long axis are conllinear, and short axle is conllinear.
Spinneret orifice is arranged as long axial symmetry, and the ratio of elliptical long axis and minor axis length is 1.8, between adjacent spinneret orifice 1.5mm is added away from the guide hole diameter equal to spinneret orifice, spinneret is round spinneret, and the diameter and series of round spinneret are oval The difference of maximum long axis length is 16mm, and the spinneret hole count of a diameter of 1.8mm of guide hole of spinneret orifice, spinneret are 300, spinneret The cross-sectional shape of the spinneret orifice of plate is hollow type.
Modified poly ester through metering, extrusion, cooling, oil and wind, modified poly ester POY is made, modified poly ester POY Spinning temperature is 281 DEG C, and cooling temperature is 22 DEG C, winding speed 3600m/min；By Modified polyester chips through metering, extrusion, It cools down, oil, stretching, thermal finalization and winding, modified poly ester FDY is made, the spinning temperature that modified poly ester is FDY is 283 DEG C, Cooling temperature is 25 DEG C, network pressure 0.23MPa, and a roller speed is 2480m/min, and a roll temperature is 78 DEG C, two roller speeds For 3690m/min, two roll temperatures are 124 DEG C, winding speed 3640m/min；Then by modified poly ester POY and modified poly ester FDY are made porous imitative hair polyester fiber through combining network, heating stretching, false twisting, thermal finalization and coiling and molding, and porous imitative hair is poly- The spinning speed of ester fiber is 590m/min, and sizing over feed rate(OFR) is 4.60%, and it is 190 DEG C that winding over feed rate(OFR), which is 3.7%, T1, T2 180 DEG C, DR 1.6, D/Y 1.7, network pressure 0.23MPa.The boiling water shrinkage of porous imitative hair polyester fiber obtained is 5.1-5.8, the spatial joint clearance Magnification of fibrous inside molecule interchain and the mechanical performance data of fiber are as follows at 120 DEG C Table.
Embodiment 58
The dyeing of porous imitative hair polyester fiber：
The porous imitative hair polyester fiber prepared to embodiment 29 dyes in high temperature and pressure machine, and actual conditions are：Dye Before color, porous imitative hair polyester fiber nonionic surfactant is handled 30 minutes at 60 DEG C, is then added in dyeing liquor, dyeing Disperse dyes dosage in liquid is 2.0% (o.w.f)；The concentration 1.2g/L of dispersant NNO, dispersant NNO；PH value is 5, bath raio It is 1:50, it is contaminated in 60 DEG C of tripping in, then heats to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C and 130 DEG C each constant temperature dyeing 1h.
General fibre is dyed using identical dyeing condition.The upper dye of porous imitative hair polyester fiber after dyed Percentage obtains by the following method：
Dye uptake is determined using raffinate colorimetric method, draws suitable dyeing stoste and dyeing residual liquid, and N, N-2 first is added The ratio of base formamide (DMF) and distilled water, DMF and water in dye liquor to be measured is 70/30 (v/v), and dye liquor absorbance is using purple Outside-visible spectrophotometer measures, and dye uptake is calculated with following formula.
In above formula, A0 and A1 are respectively the absorbance for dyeing stoste and dyeing residual liquid.
When disperse dyes are Disperse Red 3B, disperse blue SE-2R or when disperseing bright blue S-GL, porous imitative hair polyester fiber and general The dye uptake result such as following table of perforating fiber：
It is compared by the coloring of porous imitative hair polyester fiber and general fibre, it can be seen that porous imitative hair polyester fiber Coloring be substantially better than general fibre, what is also contained from the side illustration modified poly ester macromolecular of the invention prepared contains The propylene glycol segment of branch makes the increasing degree of free volume be far longer than the characteristic of unbranched polyester macromolecule chain, freely The increase of volume improves molecule and enters degree inside polyester, the free volume of polyester fiber prepared by modified polyester It is far longer than polyester fiber unbranched at same temperature, increases the diffusion of dyestuff, improves the dyeability of polyester fiber.
Embodiment 59
The dyeing of porous imitative hair polyester fiber：
The porous imitative hair polyester fiber prepared to embodiment 31 dyes in high temperature and pressure machine, and actual conditions are：Dye Before color, porous imitative hair polyester fiber nonionic surfactant is handled 30 minutes at 60 DEG C, is then added in dyeing liquor, dyeing Disperse dyes dosage in liquid is 2.0% (o.w.f)；The concentration 1.2g/L of dispersant NNO, dispersant NNO；PH value is 5, bath raio It is 1:50, it is contaminated in 60 DEG C of tripping in, then heats to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C and 130 DEG C each constant temperature dyeing 1h.
General fibre is dyed using identical dyeing condition.The upper dye of porous imitative hair polyester fiber after dyed Percentage obtains by the following method：
Dye uptake is determined using raffinate colorimetric method, draws suitable dyeing stoste and dyeing residual liquid, and N, N-2 first is added The ratio of base formamide (DMF) and distilled water, DMF and water in dye liquor to be measured is 70/30 (v/v), and dye liquor absorbance is using purple Outside-visible spectrophotometer measures, and dye uptake is calculated with following formula.
In above formula, A0 and A1 are respectively the absorbance for dyeing stoste and dyeing residual liquid.
When disperse dyes are Disperse Red 3B, disperse blue SE-2R or when disperseing bright blue S-GL, porous imitative hair polyester fiber and general The dye uptake result such as following table of perforating fiber：
It is compared by the coloring of porous imitative hair polyester fiber and general fibre, it can be seen that porous imitative hair polyester fiber Coloring be substantially better than general fibre, what is also contained from the side illustration modified poly ester macromolecular of the invention prepared contains The propylene glycol segment of branch makes the increasing degree of free volume be far longer than the characteristic of unbranched polyester macromolecule chain, freely The increase of volume improves molecule and enters degree inside polyester, the free volume of polyester fiber prepared by modified polyester It is far longer than polyester fiber unbranched at same temperature, increases the diffusion of dyestuff, improves the dyeability of polyester fiber.

Claims (9)

1. a kind of porous imitative hair polyester fiber, it is characterized in that：The material of the porous imitative hair polyester fiber is modified poly ester, described Modified poly ester is made of terephthalic acid (TPA) segment, ethylene glycol segment and propylene glycol segment containing branch；
The fiber number of the porous imitative hair polyester fiber be 150-300dtex, initial modulus≤85cN/dtex, fracture strength >= 2.1cN/dtex, elongation at break are 15.0 ± 2.0%, and crimp contraction is 5.50 ± 3.0%, and internet pricing is 90 ± 5/m； The porous imitative hair polyester fiber in the case where temperature is 80~130 DEG C, the spatial joint clearance of fibrous inside molecule interchain increases 10~ 30v/v%；Line density deviation ratio≤2.0% of the porous imitative hair polyester fiber, fracture strength CV value≤4.0%, fracture are stretched Long CV value≤8.0%, crimp contraction coefficient of variation CV value≤8.0%, boiling water shrinkage are 5.0 ± 1.0%；The molecule The spatial joint clearance increase of interchain refer to modified poly ester with normal polyester the spatial joint clearance of mutually synthermal molecule interchain comparison；
Propylene glycol containing branch is -1,3 propylene glycol of 2- amyls, -1,3 propylene glycol of 2- hexyls, -1,3 propylene glycol of 2- heptyl, 2- pungent One or more of -1,3 propylene glycol of -1,3 propylene glycol of base, -1,3 propylene glycol of 2- nonyls or 2- decyls.
2. a kind of preparation method of porous imitative hair polyester fiber as described in claim 1, it is characterized in that：Modified poly ester is used Porous imitative hair polyester fiber is made in porous spinneret spinning；The arrangement mode of spinneret orifice is that ellipse is arranged on the porous spinneret Row, the oval shaped arrangements refer to that the hole center of spinneret orifice is located on concentration ellipse, and the concentration ellipse is that series is oval, is owned Elliptical long axis is conllinear, and short axle is conllinear；
The preparation method of the porous imitative hair polyester fiber is：By modified poly ester through metering, extrusion, cooling, oil and wind, make Obtain modified poly ester POY；By Modified polyester chips through metering, extrusion, cooling, oil, stretch, thermal finalization and winding, be made and change Property polyester FDY；Then by modified poly ester POY and modified poly ester FDY through combining network, heating stretching, false twisting, thermal finalization And coiling and molding；
The preparation process of the modified poly ester is：
(1) preparation of terephthalic acid (TPA) binary alcohol esters；
After terephthalic acid (TPA) and the propylene glycol containing branch are made into slurry, under the catalytic action of the concentrated sulfuric acid, esterification is carried out Obtain terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate；
After terephthalic acid (TPA) and ethylene glycol are made into slurry, esterification is carried out, ethylene glycol terephthalate is obtained；
(3) preparation of modified poly ester；
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, stirring is mixed It closes, under the action of catalyst and stabilizer, under conditions of negative pressure, carries out polycondensation reaction and the Gao Zhen of low vacuum stage successively Modified poly ester is made in the polycondensation reaction in empty stage.
3. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that the modification is poly- The specific preparation process of ester is：
(1) preparation of terephthalic acid (TPA) binary alcohol esters；
Terephthalic acid (TPA) and the propylene glycol containing branch are made into slurry, under the catalytic action of the concentrated sulfuric acid, carry out esterification, ester Change reaction compressive reaction in nitrogen atmosphere, moulding pressure is normal pressure~0.3MPa, and temperature is 180~240 DEG C, works as esterification In water quantity of distillate be esterification terminal when reaching 90% of theoretical value or more, obtain terephthalic acid (TPA) binary alcohol esters；
(2) preparation of ethylene glycol terephthalate；
After terephthalic acid (TPA) and ethylene glycol are made into slurry, progress esterification, esterification compressive reaction in nitrogen atmosphere, Moulding pressure is normal pressure~0.3MPa, and temperature is 250~260 DEG C, when the water quantity of distillate in esterification reaches theoretical value It is esterification terminal when 90% or more, obtains ethylene glycol terephthalate；
(3) preparation of modified poly ester；
After esterification in step (2), the terephthalic acid (TPA) binary alcohol esters prepared in step (1) are added, stirring is mixed It closes 15-20 minutes, under the action of catalyst and stabilizer, starts the polycondensation reaction of low vacuum stage under conditions of negative pressure, The staged pressure by normal pressure is steadily evacuated to absolute pressure 500Pa hereinafter, temperature control is at 260~270 DEG C, and the reaction time is 30~ 50 minutes；It then proceedes to vacuumize, carries out the polycondensation reaction of high vacuum stage of Fig, so that reaction pressure is down to absolute pressure and be less than Modified poly ester is made in 275~280 DEG C, 50~90 minutes reaction time in 100Pa, reaction temperature control；
Described modified poly ester POY main spinning technology parameters are：
Spinning temperature：280-290℃；
Cooling temperature：18-22℃；
Winding speed：3200-3600m/min；
Described modified poly ester FDY main spinning technology parameters are：
Spinning temperature：280-290℃；
Cooling temperature：20-25℃；
Network pressure：0.20-0.30MPa；
One roller speed：2200-2600m/min；
One roll temperature：75-85℃；
Two roller speeds：3650-3850m/min；
Two roll temperatures：115-135℃；
Winding speed：3600-3800m/min；
The main spinning technology parameter of the porous imitative hair polyester fiber is：
Spin speed：400-800m/min；
Sizing over feed rate(OFR)：3.5-5.50%；
Wind over feed rate(OFR)：2.5-5.0%；
T1：180-220℃；
T2：150-180℃；
DR：1.6-1.8；
D/Y:1.6-2.0；
Network pressure：0.05-0.3MPa.
4. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that in step (1), The molar ratio of terephthalic acid (TPA) and the propylene glycol containing branch is 1:1.3-1.5；Concentrated sulfuric acid addition is terephthalic acid (TPA) weight 0.3-0.5%；A concentration of 50-60wt% of the concentrated sulfuric acid；
In step (2), the molar ratio of terephthalic acid (TPA) and ethylene glycol is 1:1.2~2.0；
In step (3), the Mole percent ratio of the terephthalic acid (TPA) binary alcohol esters and ethylene glycol terephthalate is 2~ 5%；The catalyst is antimony oxide, antimony glycol or antimony acetate, and catalyst charge is terephthalic acid (TPA) total weight 0.01%~0.05%；The stabilizer is triphenyl phosphate, trimethyl phosphate or Trimethyl phosphite, and stabilizer addition is The 0.01%~0.05% of the terephthalic acid (TPA) total weight；
The number-average molecular weight of the modified poly ester is 15000~30000.
5. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that the spinneret orifice Be arranged as long axis and/or short axle is symmetrical.
6. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that elliptical long axis Ratio with minor axis length is 1.3~1.8；The guide hole diameter that the spacing of adjacent spinneret orifice is more than or equal to spinneret orifice adds 1.5mm.
7. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that the spinneret For round spinneret or elliptical spinneret plate；The difference of the diameter of the circle spinneret and the oval maximum long axis length of series More than 10mm, the elliptical spinneret plate and the difference of the oval maximum long axis length of series are more than 10mm.
8. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that the spinneret orifice The a diameter of 1.5~2.5mm of guide hole；The spinneret hole count of the spinneret is more than or equal to 192.
9. a kind of preparation method of porous imitative hair polyester fiber according to claim 2, which is characterized in that the spinneret The cross-sectional shape of spinneret orifice be circle, square, diamond shape, "-" type, triangular form, trilobal cross, hollow type or platypelloid type.
CN201610781179.8A 2016-08-31 2016-08-31 Porous imitative hair polyester fiber of one kind and preparation method thereof Active CN106283259B (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102030893A (en) * 2009-09-29 2011-04-27 东丽纤维研究所（中国）有限公司 Copolyester as well as preparation method and application thereof
CN102797054A (en) * 2012-09-03 2012-11-28 江苏恒力化纤股份有限公司 Manufacturing method of high-strength, high-modulus and low-shrinkage polyester industrial yarn
CN102851757A (en) * 2011-06-30 2013-01-02 江苏华亚化纤有限公司 Special-shaped spinneret plate for spinning heavy denier yarns
JP2014189933A (en) * 2013-03-28 2014-10-06 Toray Ind Inc Normal pressure dispersion-dyeable polyester ultra-fine fiber
CN104499080A (en) * 2014-12-31 2015-04-08 江苏恒力化纤股份有限公司 High-strength activated polyester industry yarn and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102030893A (en) * 2009-09-29 2011-04-27 东丽纤维研究所（中国）有限公司 Copolyester as well as preparation method and application thereof
CN102851757A (en) * 2011-06-30 2013-01-02 江苏华亚化纤有限公司 Special-shaped spinneret plate for spinning heavy denier yarns
CN102797054A (en) * 2012-09-03 2012-11-28 江苏恒力化纤股份有限公司 Manufacturing method of high-strength, high-modulus and low-shrinkage polyester industrial yarn
JP2014189933A (en) * 2013-03-28 2014-10-06 Toray Ind Inc Normal pressure dispersion-dyeable polyester ultra-fine fiber
CN104499080A (en) * 2014-12-31 2015-04-08 江苏恒力化纤股份有限公司 High-strength activated polyester industry yarn and preparation method thereof

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