CN106350886A - High-uniformity and high-strength polyester industrial yarns and preparation method thereof - Google Patents
High-uniformity and high-strength polyester industrial yarns and preparation method thereof Download PDFInfo
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- CN106350886A CN106350886A CN201610776709.XA CN201610776709A CN106350886A CN 106350886 A CN106350886 A CN 106350886A CN 201610776709 A CN201610776709 A CN 201610776709A CN 106350886 A CN106350886 A CN 106350886A
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- phthalic acid
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- esterification
- spinneret
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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
- D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
- D01F6/84—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from copolyesters
-
- 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
-
- 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
- C08G63/78—Preparation processes
-
- 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
- D01D10/00—Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
- D01D10/02—Heat treatment
-
- 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
- D01D4/00—Spinnerette packs; Cleaning thereof
- D01D4/02—Spinnerettes
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/12—Stretch-spinning methods
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- 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
Abstract
The invention relates to high-uniformity and high-strength polyester industrial yarns and a preparation method thereof. Polyester fibers are prepared from modified polyester consisting of a terephthalic acid chain section, an ethylene glycol chain section and a branch-containing dihydric alcohol chain section. The preparation method of the high-uniformity, high-tenacity and low-elongation polyester industrial yarns comprises the following steps: performing esterification reaction on terephthalic acid and branch-containing dihydric alcohol under the catalysis of concentrated sulfuric acid to obtain phthalic acid dihydric alcohol ester; then matching the terephthalic acid and dihydric alcohol for esterification reaction to obtain terephthalate; finally, stirring and mixing the phthalic acid dihydric alcohol ester and the terephthalate, performing condensation polymerization in a low-vacuum stage and a high-vacuum stage under the action of a catalyst and a stabilizer to prepare modified polyester, and performing metering, extrusion by a multihole spinneret plate, cooling, oiling, drawing, thermal sizing and winding on the modified polyester to prepare the high-uniformity and high-strength polyester industrial yarns.
Description
Technical field
The invention belongs to polyester fiber technical field, it is related to a kind of high uniformity high-strength polyester industrial fiber and its preparation side
Method.
Background technology
Polyethylene terephthalate (pet fiber or polyester fiber) fiber since the advent of the world, have fracture strength and
Elastic modelling quantity 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 have crease-resistant exempt to provide, the advantages of stiffness is good, be widely used in the fields such as clothing, home textile.
Pet Industrial Fiber is primarily referred to as mostly being applied to industry, national defence, medical treatment, environmental conservation and most advanced branches of science each side
Face, is to have relatively special physicalchemical structure, performance and purposes, or has the chemical fibre of specific function, major embodiment
Being able to bear strong corrosion, low abrasion, high temperature resistant, radiation hardness, fire-retardant, fire-resistant, high voltage withstanding, high strength and modulus and plurality of medical work(
Energy.Using high-strength low-shrinkage polyester industrial filament yarn as the pvc shelter cloth of raw material production, there is higher peel strength and tear is strong
Degree, makes shelter cloth be applied to various uses, flexible body advertising lamp box material, inflatable structure material, fluffy lid architectural fabrics sunshade account
Paulin etc..Based on high-strength low-shrinkage industrial yarn, textile material obtains in terms of the military supplies such as special protective garment, camouflage, covering, knapsack
To application.One kind as earth working material has the advantages that light, soft, high-strength, wear-resisting, anticorrosive, non-conductive, damping.Make
Used time safe ready, efficiency high, and lifting object will not be damaged.The application of Pet Industrial Fiber is expanded and is driven application
The whole competitiveness lifting in field, no matter in the weight mitigating composite, the durability of use and minimizing are keeped in repair, are raised cost
Etc. all many-sides, polyesters high-performance fiber has increasingly given play to its synthetic competitive advantages.Following many decades, high-performance polyester
The development of fiber not only has considerable progress in quantity, more in the expansion of application and carrying of industrial chain whole competitiveness
Go up the substantial effect of acquirement.
Have many parameters during melt spinning, these parameters determine fiberizing course and spin fiber structure and
Performance, production is exactly the fiber of desired properties is obtained by controlling these parameters.Experimental branch line all adopts side for a long time
As the type of cooling, energy resource consumption accounts for the significant portion of long filament production cost, with people to chemical fibre performance and quality for blowing
Require increasingly to improve, the exploitation of chemical-fibres filaments new product develops it is desirable to higher is cold to the fibre in differentiation direction of high added value
But blowing condition, then proposes ring blowing device.Ring blowing device not only possesses the uniform advantage of every synnema wind-engaging, Er Qieneng
Consumption is compared relatively low, effectively solves the wind energy loss problem that cross air blasting causes because blowing area is big.
In spinning process, although ring blowing has obvious advantage, but still the cooling of porous yarn cannot be solved well
Uneven problem: because spun silk is after circular spinneret is extruded, by ring wind quenching, due to the circular spinneret number of turns relatively
Many lead to that the silk of innermost layer may be also uncolled after cooling in outermost silk so that ring blowing hardly enters innermost layer,
Thus the problems such as fiber number is irregular, and intensity is irregular in the silk of gained, cause follow-up to silk be processed further difficulty occurs.
Content of the invention
The technical problem to be solved in the present invention is for the deficiencies in the prior art, provides a kind of high uniformity high-strength polyester
Industrial yarn and preparation method thereof, the raw material of high uniformity high-strength polyester industrial fiber of the present invention is modified poly ester, modified poly ester
The dihydroxylic alcohols segment containing side chain for the introducing in strand, the modified high uniformity high-strength polyester industrial fiber of modified polyester preparation,
Under the conditions of uniform temperature, the increasing degree of the spatial joint clearance of high uniformity high-strength polyester industrial fiber interior molecules interchain is much big
Unbranched high uniformity high-strength polyester industrial fiber at equal temperature, the melt of high uniformity high-strength polyester industrial fiber glues
Degree reduces, and reduces processing temperature, reduces degradation rate, is conducive to processing.In addition the high uniformity high-tenacity low-elongation of the present invention gathers
On the porous spinneret of ester industrial yarn, the arrangement mode of spinneret orifice is oval shaped arrangements, and described oval shaped arrangements refer to spinneret orifice
Hole is centrally located on concentration ellipse, and described concentration ellipse is that series is oval, and all oval major axis are conllinear, and short axle is conllinear;Energy
Enough reach higher cooling effectiveness and preferable cooling effect.
A kind of high uniformity high-strength polyester industrial fiber, described high uniformity high-strength polyester industrial fiber is by modified poly ester warp
After solid-phase tack producing, spinning obtains;The material of described high uniformity high-strength polyester industrial fiber be modified poly ester, described modified poly ester by
P-phthalic acid segment, ethylene glycol segment and the composition of the dihydroxylic alcohols segment containing side chain, the described dihydroxylic alcohols segment containing side chain refers to
Side chain is located on one of dihydroxylic alcohols segment non-end group carbon and side chain is the binary of the linear carbon chain containing 5-10 carbon atom
Alcohol segment;Fracture strength >=the 8.8cn/dtex of described high uniformity high-strength polyester industrial fiber;Described high uniformity high-strength
At 260~290 DEG C, melt viscosity declines 10-20%, line density deviation ratio≤1.0%, fracture strength cv value to polyester industrial fiber
≤ 2.0%, extension at break cv value≤5.5%;
Described melt viscosity declines the contrast referring to modified poly ester and normal polyester in mutually synthermal melt viscosity.
A kind of high uniformity high-strength polyester industrial fiber is modified poly ester, introduces to contain and prop up on modified poly ester macromole long-chain
The dihydroxylic alcohols segment of chain, and the length of side chain and quantity are larger to the crystal property of modified poly ester and the impact of flow behavior,
The too short purpose not reaching polyester modification of chain length, length is oversize to cause new entanglement, affect its flow behavior, when side chain position
On one of dihydroxylic alcohols segment non-end group carbon and when side chain is the linear carbon chain containing 5-10 carbon atom, modified polyester
A kind of high uniformity high-strength polyester industrial fiber of preparation, under the conditions of uniform temperature, the space of industrial yarn interior molecules interchain
The increasing degree in gap is far longer than unbranched industrial yarn at equal temperature, is conducive to industrial yarn melt viscosity to reduce, is easy to
Further processing.
A kind of high uniformity high-strength polyester industrial fiber as above, described high uniformity high-strength polyester industrial fiber
Extension at break is 12.0 ± 1.5%, network 5 ± 2, under the test condition for 177 DEG C × 10min × 0.05cn/dtex for the temperature,
The dry-hot shrinkage of fiber is 8.5 ± 1.5%;The number-average molecular weight of described modified poly ester is 15000-30000.
A kind of high uniformity high-strength polyester industrial fiber as above, the described dihydroxylic alcohols segment containing side chain is 2- penta
Base -1,3 propylene glycol segment, 2- hexyl -1,3 propylene glycol segment, 2- heptyl -1,3 propylene glycol segment, 2- octyl group -1,3 propylene glycol chain
Section, 2- nonyl -1,3 propylene glycol segment, 2- decyl -1,3 propylene glycol segment, 2- amyl group -1,4 butanediol segment, 2- hexyl -1,4
Butanediol segment, 2- heptyl -1,4 butanediol segment, 2- octyl group -1,4 butanediol segment, 2- nonyl -1,4 butanediol segment, 2-
Decyl -1,4 butanediol segment, 2- amyl group -1,5 pentanediol segment, 2- hexyl -1,5 pentanediol segment, 2- heptyl -1,5 pentanediol
Segment, 2- octyl group -1,5 pentanediol segment, 2- nonyl -1,5 pentanediol segment, 2- decyl -1,5 pentanediol segment, 2- amyl group -1,
6 hexanediol segments, 2- hexyl -1,6 hexanediol segment, 2- heptyl -1,6 hexanediol segment, 2- octyl group -1,6 hexanediol segment, 2-
One or more of nonyl -1,6 hexanediol segment or 2- decyl -1,6 hexanediol segment;The described dihydroxylic alcohols segment containing side chain with
The Mole percent ratio of ethylene glycol segment is 2~5%.
A kind of preparation method of high uniformity high-strength polyester industrial fiber of the present invention, modified poly ester is increased through solid phase polycondensation
Viscous, metering, porous spinneret are extruded, cool down, oiling, stretching, thermal finalization and winding, prepared high uniformity high-strength polyester industrial
Silk;
On described porous spinneret, the arrangement mode of spinneret orifice is oval shaped arrangements, and described oval shaped arrangements refer to spinneret orifice
Hole be centrally located on concentration ellipse, described concentration ellipse is that series is oval, and all oval major axis are conllinear, and short axle is conllinear;
The preparation process of modified poly ester comprises the following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
P-phthalic acid is made into after slurry with the dihydroxylic alcohols containing side chain, under the catalytic action of concentrated sulphuric acid, is esterified
Reaction, obtains p-phthalic acid binary alcohol esters;It is non-that the described dihydroxylic alcohols containing side chain are that side chain is located at one of dihydroxylic alcohols segment
On end group carbon and side chain is the dihydroxylic alcohols of the linear carbon chain containing 5-10 carbon atom;
For the dihydroxylic alcohols containing side chain, its side chain is alkyl, is electron withdraw group, in the presence of side chain, makes strand
Spatial volume increases, and solvation diminishes, and in dihydroxylic alcohols, proton is difficult to dissociate so that containing dihydroxylic alcohols and the terephthaldehyde of side chain
The reactivity of acid is less than ethylene glycol, according to the mixing of same ethylene glycol and terephthaldehyde's acid reaction, can cause the binary containing side chain
Alcohol reaction is imperfect, thus ratio in polyester macromolecule for the dihydroxylic alcohols containing side chain for the impact, and then affect the performance of polyester.This
Using first the dihydroxylic alcohols containing side chain being carried out esterification with p-phthalic acid under the catalytic action of sulphuric acid, its product exists for invention
Ethylene glycol and p phthalic acid esterification add it is ensured that containing the stability of the dihydroxylic alcohols proportioning of side chain after terminating.
(2) preparation of ethylene glycol terephthalate:
P-phthalic acid and ethylene glycol are made into after slurry, carry out esterification, obtain ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), stir
Mix mixing, in the presence of catalyst and stabilizer, under conditions of negative pressure, carry out successively the coarse vacuum stage polycondensation reaction and
The polycondensation reaction of high vacuum stage of Fig, prepared modified poly ester.
A kind of preparation method of high uniformity high-strength polyester industrial fiber is it is characterised in that described modification as above
Prepared by polyester concretely comprises the following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
P-phthalic acid and the dihydroxylic alcohols containing side chain are made into slurry and add in reactor, in the catalytic action of concentrated sulphuric acid
Under, carry out esterification, esterification compressive reaction in nitrogen atmosphere, moulding pressure is normal pressure~0.3mpa, temperature is 180
~240 DEG C, be esterification terminal when the water quantity of distillate in esterification reaches more than the 90% of theoretical value;Obtain to benzene two
Formic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
P-phthalic acid and ethylene glycol are made into after slurry and add in reactor, carry out esterification, esterification is in nitrogen
Atmosphere encloses middle compressive reaction, and moulding pressure is normal pressure~0.3mpa, and temperature is 250~260 DEG C, when the water in esterification distillates
It is esterification terminal that amount reaches during more than the 90% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), stir
Mix mixing 15-20 minute, in the presence of catalyst and stabilizer, the polycondensation starting the coarse vacuum stage under conditions of negative pressure is anti-
Should, this staged pressure is steadily evacuated to below absolute pressure 500pa by normal pressure, and at 260~270 DEG C, the response time is temperature control
30~50 minutes;Then proceed to evacuation, carry out the polycondensation reaction of high vacuum stage of Fig, make reaction pressure be down to absolute pressure and be less than
100pa, reaction temperature controls at 275~280 DEG C, 50~90 minutes response time, prepared modified poly ester;
Again modified poly ester is obtained Modified polyester chips through pelletizing, obtained polyester slice is viscosified by solid phase polycondensation, makes
The intrinsic viscosity of polyester slice brings up to 1.0~1.2dl/g, as high viscous section;Again through metering, porous spinneret extrusion, cold
But, oil, stretch, thermal finalization and winding, prepared high uniformity high-strength polyester industrial fiber;
Spinning main technologic parameters are:
The temperature of described extrusion is 290~310 DEG C;
The pathogenic wind-warm of described cooling is 20~30 DEG C;
Described stretching, heat setting process parameter are: gr-1 speed 440~650m/min;75~85 DEG C of temperature;Gr-2 speed
460~680m/min;90~100 DEG C of temperature;Gr-3 speed 1900~2400m/min;125~140 DEG C of temperature;Gr-4 speed
2700~3600m/min;220~250 DEG C of temperature;Gr-5 speed 2500~3600m/min;150~170 DEG C of temperature;Described volume
Around speed be 2600~3600m/min.
A kind of preparation method of high uniformity high-strength polyester industrial fiber as above, in described step (1), to benzene two
Formic acid is 1:1.3-1.5 with the mol ratio of the dihydroxylic alcohols containing side chain;Concentrated sulphuric acid addition is the 0.3- of p-phthalic acid weight
0.5%;The concentration of described concentrated sulphuric acid is 50-60wt%;In described step (2), p-phthalic acid with the mol ratio of ethylene glycol is
1:1.2~2.0;In described step (3), the Mole percent of described p-phthalic acid binary alcohol esters and ethylene glycol terephthalate
Ratio is 2~5%;Described catalyst is antimony oxide, antimony glycol or antimony acetate, and catalyst charge is p-phthalic acid
The 0.01%~0.05% of gross weight;Described stabilizer is triphenyl phosphate, trimethyl phosphate or NSC 6513, stabilizer
Addition is the 0.01%~0.05% of described p-phthalic acid gross weight.
A kind of preparation method of high uniformity high-strength polyester industrial fiber as above, the described dihydroxylic alcohols containing side chain are
2- amyl group -1,3 propylene glycol, 2- hexyl -1,3 propylene glycol, 2- heptyl -1,3 propylene glycol, 2- octyl group -1,3 propylene glycol, 2- nonyl -1,
3 propylene glycol, 2- decyl -1,3 propylene glycol, 2- amyl group -1,4 butanediol, 2- hexyl -1,4 butanediol, 2- heptyl -1,4 butanediol,
2- octyl group -1,4 butanediol, 2- nonyl -1,4 butanediol, 2- decyl -1,4 butanediol, 2- amyl group -1,5 pentanediol, 2- hexyl -1,
5 pentanediols, 2- heptyl -1,5 pentanediol, 2- octyl group -1,5 pentanediol, 2- nonyl -1,5 pentanediol, 2- decyl -1,5 pentanediol,
2- amyl group -1,6 hexanediol, 2- hexyl -1,6 hexanediol, 2- heptyl -1,6 hexanediol, 2- octyl group -1,6 hexanediol, 2- nonyl -1,
One or more of 6 hexanediol or 2- decyl -1,6 hexanediol.
A kind of preparation method of high uniformity high-strength polyester industrial fiber as above, described porous spinneret is circle
Spinneret or elliptical spinneret plate;The diameter of described circle spinneret is more than with the difference of the oval maximum long axis length of series
10mm, described elliptical spinneret plate is more than 10mm with the difference of the oval maximum long axis length of series.
A kind of preparation method of high uniformity high-strength polyester industrial fiber as above, spray webbing on described porous spinneret
Hole be arranged as that major axis and/or short axle are symmetrical, the guide hole diameter that the spacing of adjacent spinneret orifice is more than or equal to spinneret orifice adds
1.5mm;Oval major axis is 1.3~1.8 with the ratio of minor axis length.
When the effective area phase of spinneret is simultaneously as the girth of ellipse is more than circular girth, spinneret orifice is oval
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, therefore, spray
Silk hole oval shaped arrangements are conducive to the cooling of ring blowing, improve the cooling effectiveness of ring blowing, the fibre property of preparation is also more excellent
Good.Major axis is closer to 1 with the ratio of minor axis length, and ellipse is more similar to justify, and the difference of cooling effectiveness and cooling effect is little;
When the ratio of major axis and minor axis length is 1.3, cooling effect significantly improves, and individual pen hole count is corresponding to increase by 16%;Major axis and short axle
When the ratio of length is 1.8, cooling effect improves larger, the corresponding increase by 33% of individual pen hole count;In the case of identical hole count, the present invention
Oval shaped arrangements reduce than the number of turns of conventional concentric circle best-fit it is easy to cooling wind thoroughly, makes the fiber cooling condition of Internal and external cycle
Evenly;When the ratio of major axis and minor axis length is more than 1.8, ellipse is partial to form flat shape, is difficult to punch, simultaneously cold
But effect no longer raises.Therefore, the oval major axis of series and the ratio of minor axis length are 1.3~1.8, can reach higher cold
But efficiency and preferable cooling effect.
A kind of preparation method of high uniformity high-strength polyester industrial fiber as above, the guide hole diameter of described spinneret orifice
For 1.5~2.5mm;The spray webbing hole count of described spinneret is more than or equal to 192, the shape of cross section of the spinneret orifice of described spinneret
For circle, square, rhombus, yi word pattern, triangular form, trilobal cross, hollow type or platypelloid type.
The principle of the present invention is:
The raw material of the high uniformity high-strength polyester industrial fiber of the present invention is modified poly ester, contains in modified poly ester macromole
The dihydroxylic alcohols segment containing side chain, when temperature is higher than vitrification point, side chain prior to backbone motion, modified polyester preparation
The free volume of industrial yarn is far longer than unbranched industrial yarn at equal temperature, advantageously reduces its melt viscosity.
On the spinneret of the present invention, the arrangement mode of spinneret orifice is oval shaped arrangements, when the effective area of spinneret is identical,
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
More preferably, the industrial yarn of preparation is also more excellent for cooling effect.When the effective area of spinneret is identical, spinneret orifice oval shaped arrangements
Hole count is more than the hole count of circular arrangement, and oval shaped arrangements are capable of greatly cooling down, and significantly improve cooling effectiveness.
Beneficial effect:
The raw material of the high uniformity high-strength polyester industrial fiber of gained of the present invention is modified poly ester, in modified poly ester macromole
The dihydroxylic alcohols segment containing side chain containing, when temperature is higher than vitrification point, side chain, prior to backbone motion, makes free volume
Increasing degree is far longer than the characteristic of unbranched polyester macromolecule chain, and the increase of free volume advantageously reduces melt viscosity,
Improve its processing characteristics.
The raw material of the high uniformity high-strength polyester industrial fiber of gained of the present invention is modified poly ester, the dihydroxylic alcohols chain containing side chain
The introducing of section to the structural regularity of modified poly ester there is no big destruction, maintain the premium properties of polyester fiber.
On the high uniformity high-strength polyester industrial fiber spinneret of the present invention, the arrangement mode of spinneret orifice is oval shaped arrangements,
When the effective area of spinneret is identical, 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
Blow through dynamic analysis of spinning, more preferably, the fibre property of preparation is also more excellent for the cooling effect of dynamic analysis of spinning.
On the high uniformity high-strength polyester industrial fiber spinneret of the present invention, the arrangement mode of spinneret orifice is oval shaped arrangements,
When the effective area of spinneret is identical, the hole count of spinneret orifice oval shaped arrangements is more than the hole count of circular arrangement, oval shaped arrangements energy
Enough realizations greatly cool down, and significantly improve cooling effectiveness.
Brief description
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
Degree ratio is 1.3;
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
Degree ratio is 1.6.
Specific embodiment
With reference to specific embodiment, the present invention is expanded on further.It should be understood that these embodiments are merely to illustrate this
Bright rather than limit the scope of the present invention.In addition, it is to be understood that after having read the content of present invention instruction, art technology
Personnel can make various changes or modifications to the present invention, and these equivalent form of values equally fall within the application appended claims and limited
Fixed scope.
Embodiment 1
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.3 for the mol ratio and 2- amyl group -1,3 propylene glycol are made into slurry and add in reactor,
Concentration is 50wt%, and addition is under the catalytic action of 0.3% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is normal pressure, and temperature is 180 DEG C, when the water in esterification distillates
It is esterification terminal that amount reaches during the 90% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.2 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is normal pressure, and temperature is 250 DEG C, when the water in esterification distillates
It is esterification terminal that amount reaches during the 90% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 2% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 15 minutes is adding
Measure for p-phthalic acid gross weight 0.01% the catalytic antimony trioxide and addition be p-phthalic acid gross weight
Under conditions of negative pressure, in the presence of 0.01% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
It is 500pa that section pressure is steadily evacuated to absolute pressure by normal pressure, and at 260 DEG C, the response time is 30 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 100pa, and reaction temperature controls
275 DEG C, 50 minutes response time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 15000, and modified poly ester is by p-phthalic acid segment, ethylene glycol segment and 2- penta
Base -1,3 propylene glycol segment compositions, the dihydroxylic alcohols segment containing side chain is 2% with the Mole percent ratio of ethylene glycol segment.
Table 1: embodiment 2-12 important technological parameters
Embodiment 2
The preparation process of the preparation method of the modified poly ester of embodiment 2, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 16 minutes, in addition be
The catalytic antimony trioxide of the 0.011% of p-phthalic acid gross weight and addition are the 0.02% of p-phthalic acid gross weight
Stabilizer triphenyl phosphate in the presence of, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure
Absolute pressure 490pa is steadily evacuated to by normal pressure, at 262 DEG C, the response time is 31 minutes to temperature control;Then proceed to evacuation,
Carry out the polycondensation reaction of high vacuum stage of Fig, make reaction pressure be down to absolute pressure 90pa, reaction temperature controls at 276 DEG C, reaction
51 minutes time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 16000, and modified poly ester is own by p-phthalic acid segment, ethylene glycol segment and 2-
Base -1,3 propylene glycol segment compositions, 2- hexyl -1,3 propylene glycol segments are 2.1% with the Mole percent ratio of ethylene glycol segment.
Embodiment 3
The preparation process of the preparation method of the modified poly ester of embodiment 3, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 16 minutes, in addition be
The catalytic antimony trioxide of the 0.03% of p-phthalic acid gross weight and addition are the 0.02% of p-phthalic acid gross weight
Stabilizer triphenyl phosphate in the presence of, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure
Absolute pressure 498pa is steadily evacuated to by normal pressure, at 263 DEG C, the response time is 32 minutes to temperature control;Then proceed to evacuation,
Carry out the polycondensation reaction of high vacuum stage of Fig, make reaction pressure be down to absolute pressure 90pa, reaction temperature controls at 277 DEG C, reaction
57 minutes time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 15900, and modified poly ester is by p-phthalic acid segment, ethylene glycol segment and 2- heptan
Base -1,3 propylene glycol segment compositions, 2- heptyl -1,3 propylene glycol segments are 2.2% with the Mole percent ratio of ethylene glycol segment.
Embodiment 4
The preparation process of the preparation method of the modified poly ester of embodiment 4, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 17 minutes, in addition be
The catalytic antimony trioxide of the 0.033% of p-phthalic acid gross weight and addition are p-phthalic acid gross weight
Under conditions of negative pressure, in the presence of 0.023% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
It is 497pa that section pressure is steadily evacuated to absolute pressure by normal pressure, and at 264 DEG C, the response time is 33 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 80pa, and reaction temperature controls
278 DEG C, 58 minutes response time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 15800, and modified poly ester is pungent by p-phthalic acid segment, ethylene glycol segment and 2-
Base -1,3 propylene glycol segment compositions, 2- octyl group -1,3 propylene glycol segments are 2.3% with the Mole percent ratio of ethylene glycol segment.
Embodiment 5
The preparation process of the preparation method of the modified poly ester of embodiment 5, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 17 minutes, in addition be
The catalytic antimony trioxide of the 0.034% of p-phthalic acid gross weight and addition are p-phthalic acid gross weight
Under conditions of negative pressure, in the presence of 0.024% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 496pa by normal pressure, and at 265 DEG C, the response time is 34 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 80pa, and reaction temperature controls 277
DEG C, 59 minutes response time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 15900, and modified poly ester is by p-phthalic acid segment, ethylene glycol segment and 2- nonyl
Base -1,3 propylene glycol segment compositions, 2- nonyl -1,3 propylene glycol segments are 2.4% with the Mole percent ratio of ethylene glycol segment.
Embodiment 6
The preparation process of the preparation method of the modified poly ester of embodiment 6, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 18 minutes, in addition be
The catalytic antimony trioxide of the 0.035% of p-phthalic acid gross weight and addition are p-phthalic acid gross weight
Under conditions of negative pressure, in the presence of 0.025% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 495pa by normal pressure, and at 266 DEG C, the response time is 35 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 70pa, and reaction temperature controls 278
DEG C, 60 minutes response time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 16000, and modified poly ester is by p-phthalic acid segment, ethylene glycol segment and the 2- last of the ten Heavenly stems
Base -1,3 propylene glycol segment compositions, 2- decyl -1,3 propylene glycol segments are 2.5% with the Mole percent ratio of ethylene glycol segment.
Embodiment 7
The preparation process of the preparation method of the modified poly ester of embodiment 7, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 19 minutes, in addition be
The catalytic antimony trioxide of the 0.036% of p-phthalic acid gross weight and addition are p-phthalic acid gross weight
Under conditions of negative pressure, in the presence of 0.025% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 496pa by normal pressure, and at 267 DEG C, the response time is 36 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 70pa, and reaction temperature controls 278
DEG C, 61 minutes response time, prepared 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 group-Isosorbide-5-Nitrae butanediol segment composition, 2- amyl group-Isosorbide-5-Nitrae butanediol segment and second two
The Mole percent ratio of alcohol segment is 2.6%.
Embodiment 8
The preparation process of the preparation method of the modified poly ester of embodiment 8, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 19 minutes, in addition be
The catalytic antimony trioxide of the 0.036% of p-phthalic acid gross weight and addition are p-phthalic acid gross weight
Under conditions of negative pressure, in the presence of 0.025% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 496pa by normal pressure, and at 267 DEG C, the response time is 36 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 70pa, and reaction temperature controls 278
DEG C, 61 minutes response time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 17000, and modified poly ester is own by p-phthalic acid segment, ethylene glycol segment and 2-
Base-Isosorbide-5-Nitrae butanediol segment composition, 2- hexyl-Isosorbide-5-Nitrae butanediol segment is 2.7% with the Mole percent ratio of ethylene glycol segment.
Embodiment 9
The preparation process of the preparation method of the modified poly ester of embodiment 9, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 16 minutes, in addition be
The catalyst glycol antimony of the 0.04% of p-phthalic acid gross weight and addition are the 0.026% of p-phthalic acid gross weight
In the presence of stabilizer trimethyl phosphate, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to absolute pressure 497pa, and at 268 DEG C, the response time is 38 minutes to temperature control;Then proceed to evacuation, enter
The polycondensation reaction of row high vacuum stage of Fig, making reaction pressure be down to absolute pressure is 60pa, and reaction temperature controls at 279 DEG C, reaction
62 minutes time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 17000, and modified poly ester is by p-phthalic acid segment, ethylene glycol segment and 2- heptan
Base-Isosorbide-5-Nitrae butanediol segment composition, 2- heptyl-Isosorbide-5-Nitrae butanediol segment is 2.8% with the Mole percent ratio of ethylene glycol segment.
Embodiment 10
The preparation process of the preparation method of the modified poly ester of embodiment 10, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 17 minutes, in addition be
The catalyst glycol antimony of the 0.03% of p-phthalic acid gross weight and addition are the 0.027% of p-phthalic acid gross weight
In the presence of stabilizer trimethyl phosphate, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to absolute pressure 498pa, and at 269 DEG C, the response time is 39 minutes to temperature control;Then proceed to evacuation, enter
The polycondensation reaction of row high vacuum stage of Fig, making reaction pressure be down to absolute pressure is 60pa, and reaction temperature controls at 278 DEG C, reaction
64 minutes time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 17000, and modified poly ester is pungent by p-phthalic acid segment, ethylene glycol segment and 2-
Base-Isosorbide-5-Nitrae butanediol segment composition, 2- octyl group-Isosorbide-5-Nitrae butanediol segment is 3% with the Mole percent ratio of ethylene glycol segment.
Embodiment 11
The preparation process of the preparation method of the modified poly ester of embodiment 11, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 18 minutes, in addition be
The catalyst glycol antimony of the 0.04% of p-phthalic acid gross weight and addition are the 0.03% of p-phthalic acid gross weight
In the presence of stabilizer trimethyl phosphate, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to absolute pressure 497pa, and at 260 DEG C, the response time is 40 minutes to temperature control;Then proceed to evacuation, enter
The polycondensation reaction of row high vacuum stage of Fig, making reaction pressure be down to absolute pressure is 60pa, and reaction temperature controls at 277 DEG C, reaction
63 minutes time, prepared modified poly ester.
The number-average molecular weight of modified poly ester is 18000, and modified poly ester is by p-phthalic acid segment, ethylene glycol segment and 2- nonyl
Base-Isosorbide-5-Nitrae butanediol segment composition, 2- nonyl-Isosorbide-5-Nitrae butanediol segment is 4% with the Mole percent ratio of ethylene glycol segment.
Embodiment 12
The preparation process of the preparation method of the modified poly ester of embodiment 2, wherein modified poly ester with embodiment 1, wherein mainly
Technical parameter referring to table 1;After step (3) adds p-phthalic acid binary alcohol esters, stirring mixing 18 minutes, in addition be
The catalyst acetic acid antimony of the 0.038% of p-phthalic acid weight and addition are the stabilizer of the 0.03% of p-phthalic acid weight
Under conditions of negative pressure, in the presence of NSC 6513, start the polycondensation reaction in coarse vacuum stage, this staged pressure is by normal pressure
Steadily it is evacuated to absolute pressure 497pa, at 265 DEG C, the response time is 42 minutes to temperature control;Then proceed to evacuation, carry out height
The polycondensation reaction of vacuum stages, making reaction pressure be down to absolute pressure is 40pa, and reaction temperature controls at 277 DEG C, the response time
70 minutes, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 26000, by p-phthalic acid segment, ethylene glycol segment and the 2- last of the ten Heavenly stems
Base-Isosorbide-5-Nitrae butanediol segment composition, 2- decyl-Isosorbide-5-Nitrae butanediol segment is 4% with the Mole percent ratio of ethylene glycol segment.
Embodiment 13
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.5 for the mol ratio and 2- decyl -1,6 hexanediol are made into slurry and add in reactor,
Concentration is 60wt%, and addition is under the catalytic action of 0.5% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.3mpa, and temperature is 240 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:2.0 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.3mpa, and temperature is 260 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 5% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 20 minutes is adding
Measure for p-phthalic acid weight 0.05% catalyst acetic acid antimony and addition be p-phthalic acid weight 0.05% steady
In the presence of determining agent NSC 6513, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure by
It is 450pa that normal pressure is steadily evacuated to absolute pressure, and at 270 DEG C, the response time is 50 minutes to temperature control;Then proceed to evacuation,
Carry out the polycondensation reaction of high vacuum stage of Fig, making reaction pressure be down to absolute pressure is 30pa, and reaction temperature controls at 280 DEG C, instead
90 minutes between seasonable, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 30000, by p-phthalic acid segment, ethylene glycol segment and the 2- last of the ten Heavenly stems
Base -1,6 hexanediol segment compositions, 2- decyl -1,6 hexanediol segments are 5% with the Mole percent ratio of ethylene glycol segment.
Embodiment 14
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.47 for the mol ratio and 2- nonyl -1,6 hexanediol are made into slurry and add in reactor,
Concentration is 60wt%, and addition is under the catalytic action of 0.47% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 220 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.8 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 258 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Measure for p-phthalic acid weight 0.04% catalyst glycol antimony and addition be the 0.04% of p-phthalic acid weight
In the presence of stabilizer trimethyl phosphate, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to absolute pressure 460pa, and at 263 DEG C, the response time is 47 minutes to temperature control;Then proceed to evacuation, enter
The polycondensation reaction of row high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, and reaction temperature controls at 278 DEG C, during reaction
Between 85 minutes, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 28000, by p-phthalic acid segment, ethylene glycol segment and 2- nonyl
Base -1,6 hexanediol segment compositions, 2- nonyl -1,6 hexanediol segments are 4% with the Mole percent ratio of ethylene glycol segment.
Embodiment 15
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.46 for the mol ratio and 2- octyl group -1,6 hexanediol are made into slurry and add in reactor,
Concentration is 60wt%, and addition is under the catalytic action of 0.49% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 233 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.8 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 259 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.5% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 19 minutes is adding
Entering 0.044% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.046% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 490pa by normal pressure, and at 269 DEG C, the response time is 48 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, and reaction temperature controls at 279 DEG C,
87 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 29000, pungent by p-phthalic acid segment, ethylene glycol segment and 2-
Base -1,6 hexanediol segment compositions, 2- octyl group -1,6 hexanediol segments are 4.5% with the Mole percent ratio of ethylene glycol segment.
Embodiment 16
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.49 for the mol ratio and 2- heptyl -1,6 hexanediol are made into slurry and add in reactor,
Concentration is 60wt%, and addition is under the catalytic action of 0.48% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 230 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.8 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 258 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.7% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 19 minutes is adding
Entering 0.048% catalyst glycol antimony that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.047% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 460pa by normal pressure, and at 267 DEG C, the response time is 48 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, and reaction temperature controls at 279 DEG C,
83 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 27000, by p-phthalic acid segment, ethylene glycol segment and 2- heptan
Base -1,6 hexanediol segment compositions, 2- heptyl -1,6 hexanediol segments are 4.7% with the Mole percent ratio of ethylene glycol segment.
Embodiment 17
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.467 for the mol ratio and 2- hexyl -1,6 hexanediol are made into slurry and add in reactor,
It is 60wt% in concentration, addition is under the catalytic action of 0.47% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 236 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.89 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 258 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.3% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.04% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.041% stabilizer NSC 6513, start the polycondensation reaction in coarse vacuum stage, should
Staged pressure is steadily evacuated to absolute pressure 490pa by normal pressure, and at 268 DEG C, the response time is 48 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, reaction temperature controls 278
DEG C, 85 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 29000, own by p-phthalic acid segment, ethylene glycol segment and 2-
Base -1,6 hexanediol segment compositions, 2- hexyl -1,6 hexanediol segments are 4.3% with the Mole percent ratio of ethylene glycol segment.
Embodiment 18
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.48 for the mol ratio and 2- amyl group -1,6 hexanediol are made into slurry and add in reactor,
Concentration is 55wt%, and addition is under the catalytic action of 0.46% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 230 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.88 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 256 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.7% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.047% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.047% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 480pa by normal pressure, and at 265 DEG C, the response time is 47 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, and reaction temperature controls at 279 DEG C,
85 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 28000, by p-phthalic acid segment, ethylene glycol segment and 2- penta
Base -1,6 hexanediol segment compositions, 2- amyl group -1,6 hexanediol segments are 4.7% with the Mole percent ratio of ethylene glycol segment.
Embodiment 19
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.46 for the mol ratio and 2- decyl -1,5 pentanediols are made into slurry and add in reactor,
Concentration is 55wt%, and addition is under the catalytic action of 0.47% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 238 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.9 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 259 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during more than the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.7% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 19 minutes is adding
Entering the 0.046% catalyst acetic acid antimony that amount is p-phthalic acid weight and addition is the 0.048% of p-phthalic acid weight
Stabilizer NSC 6513 in the presence of, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this stage press
It is 446pa that power is steadily evacuated to absolute pressure by normal pressure, and at 267 DEG C, the response time is 49 minutes to temperature control;Then proceed to take out very
Sky, carries out the polycondensation reaction of high vacuum stage of Fig, and making reaction pressure be down to absolute pressure is 40pa, and reaction temperature controls at 278 DEG C,
87 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 29000, by p-phthalic acid segment, ethylene glycol segment and the 2- last of the ten Heavenly stems
Base -1,5 pentanediol segment compositions, 2- decyl -1,5 pentanediol segments are 4.7% with the Mole percent ratio of ethylene glycol segment.
Embodiment 20
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.46 for the mol ratio and 2- nonyl -1,5 pentanediols are made into slurry and add in reactor,
Concentration is 60wt%, and addition is under the catalytic action of 0.46% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.26mpa, and temperature is 221 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.89 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.25mpa, and temperature is 259 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.1% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.041% catalyst glycol antimony that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.042% stabilizer trimethyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 460pa by normal pressure, and at 265 DEG C, the response time is 47 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, and reaction temperature controls at 278 DEG C,
85 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 28000, by p-phthalic acid segment, ethylene glycol segment and 2- nonyl
Base -1,5 pentanediol segment compositions, 2- nonyl -1,5 pentanediol segments are 4.1% with the Mole percent ratio of ethylene glycol segment.
Embodiment 21
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.43 for the mol ratio and 2- octyl group -1,5 pentanediols are made into slurry and add in reactor,
Concentration is 60wt%, and addition is under the catalytic action of 0.47% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 235 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.78 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.26mpa, and temperature is 255 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.3% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 17 minutes is adding
Entering 0.043% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.049% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 490pa by normal pressure, and at 268 DEG C, the response time is 46 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 40pa, and reaction temperature controls at 275 DEG C,
85 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 28000, pungent by p-phthalic acid segment, ethylene glycol segment and 2-
Base -1,5 pentanediol segment compositions, 2- octyl group -1,5 pentanediol segments are 4.3% with the Mole percent ratio of ethylene glycol segment.
Embodiment 22
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.43 for the mol ratio and 2- heptyl -1,5 pentanediols are made into slurry and add in reactor,
Concentration is 55wt%, and addition is under the catalytic action of 0.45% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.29mpa, and temperature is 235 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.87 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 255 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.6% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.047% catalyst glycol antimony that amount is p-phthalic acid weight and addition is the 0.04% of p-phthalic acid weight
Stabilizer triphenyl phosphate in the presence of, under conditions of negative pressure start the coarse vacuum stage polycondensation reaction, this staged pressure
Absolute pressure 470pa is steadily evacuated to by normal pressure, at 268 DEG C, the response time is 45 minutes to temperature control;Then proceed to evacuation,
Carry out the polycondensation reaction of high vacuum stage of Fig, make reaction pressure be down to absolute pressure 40pa, reaction temperature controls at 279 DEG C, reaction
83 minutes time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 29000, by p-phthalic acid segment, ethylene glycol segment and 2- heptan
Base -1,5 pentanediol segment compositions, 2- heptyl -1,5 pentanediol segments are 4.6% with the Mole percent ratio of ethylene glycol segment.
Embodiment 23
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.457 for the mol ratio and 2- hexyl -1,5 pentanediols are made into slurry and add in reactor,
It is 55% in concentration, addition is under the catalytic action of 0.46% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 239 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.81 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 255 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.41% with the Mole percent ratio of ethylene glycol terephthalate, stirring mixing 19 minutes,
Addition is 0.042% the catalytic antimony trioxide of p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.048% stabilizer NSC 6513, start the polycondensation reaction in coarse vacuum stage, should
Staged pressure is steadily evacuated to absolute pressure 495pa by normal pressure, and at 265 DEG C, the response time is 45 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 50pa, reaction temperature controls 275
DEG C, 85 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 28000, own by p-phthalic acid segment, ethylene glycol segment and 2-
Base -1,5 pentanediol segment compositions, 2- hexyl -1,5 pentanediol segments are 4.41% with the Mole percent ratio of ethylene glycol segment.
Embodiment 24
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
By the p-phthalic acid for 1:1.47 for the mol ratio and 2- amyl group -1,5 pentanediols are made into slurry and add in reactor,
Concentration is 55wt%, and addition is under the catalytic action of 0.48% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 245 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.81 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 259 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.67% with the Mole percent ratio of ethylene glycol terephthalate, stirring mixing 19 minutes,
Addition is 0.041% the catalytic antimony trioxide of p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.042% stabilizer triphenyl phosphate, start the polycondensation reaction in coarse vacuum stage, this rank
Section pressure is steadily evacuated to absolute pressure 485pa by normal pressure, and at 268 DEG C, the response time is 46 minutes to temperature control;Then proceed to take out
Vacuum, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 50pa, and reaction temperature controls at 275 DEG C,
89 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 29000, by p-phthalic acid segment, ethylene glycol segment and 2- penta
Base -1,5 pentanediol segment compositions, 2- amyl group -1,5 pentanediol segments are 4.67% with the Mole percent ratio of ethylene glycol segment.
Embodiment 25
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
The p-phthalic acid for 1:1.45 for the mol ratio and 2- hexyl -1,5 pentanediol and 2- amyl group -1,4 butanediol is mixed
Compound is made into slurry and adds in reactor, wherein 2- hexyl -1, and the mol ratio of 5 pentanediols and 2- amyl group-Isosorbide-5-Nitrae butanediol is 3:1,
It is 55% in concentration, addition is under the catalytic action of 0.49% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.26mpa, and temperature is 236 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.8 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 258 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.4% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.042% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.047% stabilizer NSC 6513, start the polycondensation reaction in coarse vacuum stage, should
Staged pressure is steadily evacuated to absolute pressure 495pa by normal pressure, and at 265 DEG C, the response time is 49 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 50pa, reaction temperature controls 278
DEG C, 88 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester be 29000, by p-phthalic acid segment, ethylene glycol segment, 2- hexyl-
1,5 pentanediol segment and 2- amyl group-Isosorbide-5-Nitrae butanediol segment composition, 2- hexyl -1,5 pentanediol segments and 2- amyl group-Isosorbide-5-Nitrae fourth 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 p-phthalic acid binary alcohol esters:
By 2- octyl group -1,6 hexanediol of the p-phthalic acid sum for 1:1.45 for the mol ratio and 2- amyl group -1,5 pentanediol
Mixture is made into slurry and adds in reactor, wherein 2- octyl group -1,6 hexanediol and 2- amyl group -1, and the mol ratio of 5 pentanediols is 3:
2, it is 60% in concentration, addition is under the catalytic action of 0.45% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 239 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.84 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification anti-
Should, esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.29mpa, and temperature is 255 DEG C, when in esterification
It is esterification terminal that water quantity of distillate reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.6% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.0423% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.045% stabilizer NSC 6513, start the polycondensation reaction in coarse vacuum stage, should
Staged pressure is steadily evacuated to absolute pressure 495pa by normal pressure, and at 265 DEG C, the response time is 45 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 50pa, reaction temperature controls 278
DEG C, 85 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester be 28000, by p-phthalic acid segment, ethylene glycol segment, 2- octyl group-
1,6 hexanediol segment and 2- amyl group -1,5 pentanediol segment compositions, 2- octyl group -1,6 hexanediol segments and 2- amyl group -1,5 penta 2
Alcohol segment is 4.6% with the Mole percent ratio of ethylene glycol segment.
Embodiment 27
A kind of preparation method of modified poly ester, specifically includes following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
The p-phthalic acid for 1:1.45 for the mol ratio and 2- hexyl -1,5 pentanediol and 2- amyl group -1,4 butanediol is mixed
Compound is made into slurry and adds in reactor, wherein 2- hexyl -1, and the mol ratio of 5 pentanediols and 2- amyl group-Isosorbide-5-Nitrae butanediol is 3:1,
It is 55% in concentration, addition is under the catalytic action of 0.49% concentrated sulphuric acid of p-phthalic acid weight, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.26mpa, and temperature is 236 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 96% of theoretical value, obtains p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.8 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.28mpa, and temperature is 258 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.4% with the Mole percent ratio of ethylene glycol terephthalate, and stirring mixing 18 minutes is adding
Entering 0.042% the catalytic antimony trioxide that amount is p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.047% stabilizer NSC 6513, start the polycondensation reaction in coarse vacuum stage, should
Staged pressure is steadily evacuated to absolute pressure 495pa by normal pressure, and at 265 DEG C, the response time is 49 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 50pa, reaction temperature controls 278
DEG C, 88 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester be 29000, by p-phthalic acid segment, ethylene glycol segment, 2- hexyl-
1,5 pentanediol segment and 2- amyl group-Isosorbide-5-Nitrae butanediol segment composition, 2- hexyl -1,5 pentanediol segments and 2- amyl group-Isosorbide-5-Nitrae fourth 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 p-phthalic acid binary alcohol esters:
The p-phthalic acid for 1:1.45 for the mol ratio is own with 2- octyl group -1,3 propylene glycol, 2- amyl group -1,4 butanediol and 2-
Base -1, the mixture of 6 hexanediol is made into slurry and adds in reactor, wherein 2- octyl group -1,3 propylene glycol, 2- amyl group-Isosorbide-5-Nitrae fourth two
Alcohol and 2- hexyl -1, the mol ratio of 6 hexanediol is 3:2:1, is 60% in concentration, and addition is p-phthalic acid weight
Under the catalytic action of 0.47% concentrated sulphuric acid, carry out esterification, esterification compressive reaction in nitrogen atmosphere, moulding pressure
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 p-phthalic acid binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
By mol ratio be 1:1.8 p-phthalic acid and ethylene glycol is made into after slurry and adds in reactor, carries out esterification,
Esterification compressive reaction in nitrogen atmosphere, moulding pressure is 0.27mpa, and temperature is 258 DEG C, when the water in esterification evaporates
It is esterification terminal that output reaches during the 92% of theoretical value, obtains ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), right
Phthalic acid binary alcohol esters are 4.71% with the Mole percent ratio of ethylene glycol terephthalate, stirring mixing 18 minutes,
Addition is 0.04% the catalytic antimony trioxide of p-phthalic acid weight and addition is p-phthalic acid weight
Under conditions of negative pressure, in the presence of 0.041% stabilizer NSC 6513, start the polycondensation reaction in coarse vacuum stage, should
Staged pressure is steadily evacuated to absolute pressure 490pa by normal pressure, and at 268 DEG C, the response time is 49 minutes to temperature control;Then proceed to
Evacuation, carries out the polycondensation reaction of high vacuum stage of Fig, makes reaction pressure be down to absolute pressure 50pa, reaction temperature controls 277
DEG C, 84 minutes response time, prepared modified poly ester.
The number-average molecular weight of prepared modified poly ester is 29000, by p-phthalic acid segment, ethylene glycol segment, band side chain
Glycol segment composition, wherein branched glycol segment be 2- octyl group -1,3 propylene glycol segments, 2- amyl group-Isosorbide-5-Nitrae butanediol chain
Section and 2- hexyl -1,6 hexanediol segments form, and branched glycol segment with the Mole percent ratio of ethylene glycol segment is
4.71%.
Embodiment 29
A kind of preparation method of high uniformity high-strength polyester industrial fiber, high uniformity high-strength polyester industrial fiber is using many
Hole spinneret is obtained, and on spinneret, the arrangement mode of spinneret orifice is oval shaped arrangements, and oval shaped arrangements refer in the hole of spinneret orifice
The heart is located on concentration ellipse, and concentration ellipse is that series is oval, and all oval major axis are conllinear, and short axle is conllinear.
As shown in figure 1, the major axis of ellipse is 1.3 with the ratio of minor axis length, the spacing of adjacent spinneret orifice is equal to spinneret orifice
Guide hole diameter add 1.5mm, spinneret is circular spinneret, the diameter of circular spinneret oval maximum long axial length with series
The difference of degree is 11mm, a diameter of 2.0mm of guide hole of spinneret orifice, and the spray webbing hole count of spinneret is 374, the spinneret orifice of spinneret
Shape of cross section be circle.
The modified poly ester that embodiment 1 is obtained is extruded, cools down, oils, is drawn through solid phase polycondensation thickening, metering, porous spinneret
Stretch, thermal finalization and winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion be 280 DEG C, the pathogenic wind-warm of cooling
For 20 DEG C, gr-1 speed 440m/min;80 DEG C of temperature;Gr-2 speed 680m/min;100 DEG C of temperature;Gr-3 speed 2000m/
min;130 DEG C of temperature;Gr-4 speed 2700m/min;240 DEG C of temperature;Gr-5 speed 3000m/min;160 DEG C of temperature;Winding
Speed is 3000m/min.
The fracture strength of prepared high uniformity high-strength polyester industrial fiber is 8.9cn/dtex;Line density deviation ratio is
0.6%, fracture strength cv value is 1.8%, and extension at break cv value is 4.5%, and extension at break is 12.0, network 6, at 260 DEG C,
Melt viscosity declines 11%, under the test condition for 177 DEG C × 10min × 0.05cn/dtex for the temperature, the dry shrinkage of fiber
Rate is 8.0%.
Embodiment 30
A kind of preparation method of high uniformity high-strength polyester industrial fiber:
As shown in figure 3, the major axis of ellipse is 1.6 with the ratio of minor axis length, the spacing of adjacent spinneret orifice is equal to spinneret orifice
Guide hole diameter add 1.5mm, spinneret is circular spinneret, the diameter of circular spinneret oval maximum long axial length with series
The difference of degree is 11mm, a diameter of 2.0mm of guide hole of spinneret orifice, and the spray webbing hole count of spinneret is 382, the spinneret orifice of spinneret
Shape of cross section be circle.
The modified poly ester that embodiment 1 is obtained is extruded, cools down, oils, is drawn through solid phase polycondensation thickening, metering, porous spinneret
Stretch, thermal finalization and winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion be 280 DEG C, the pathogenic wind-warm of cooling
For 20 DEG C, gr-1 speed 440m/min;80 DEG C of temperature;Gr-2 speed 680m/min;100 DEG C of temperature;Gr-3 speed 2000m/
min;130 DEG C of temperature;Gr-4 speed 2700m/min;240 DEG C of temperature;Gr-5 speed 3000m/min;160 DEG C of temperature;Winding
Speed is 3000m/min.
The fracture strength of prepared high uniformity high-strength polyester industrial fiber is 8.8cn/dtex;Line density deviation ratio is
0.7%, fracture strength cv value is 1.7%, and extension at break cv value is 4.8%, and extension at break is 12.1, network 6, at 260 DEG C,
Melt viscosity declines 11%, under the test condition for 177 DEG C × 10min × 0.05cn/dtex for the temperature, the dry shrinkage of fiber
Rate is 8.2%.
Comparative example 1
A kind of preparation method of high uniformity high-strength polyester industrial fiber, high uniformity high-strength polyester industrial fiber is using many
Hole spinneret is obtained, and on spinneret, the arrangement mode of spinneret orifice is circular arrangement, and circular arrangement refers to the hole centre bit of spinneret orifice
On concentric circular, concentric circular is that series is circular.As shown in Fig. 2 the guide hole diameter that the spacing of adjacent spinneret orifice is equal to spinneret orifice adds
Upper 1.5mm, spinneret is circular spinneret, and the diameter of circular spinneret is 11mm with the difference of the circular maximum diameter of series,
The a diameter of 2.0mm of guide hole of spinneret orifice, the spray webbing hole count of spinneret is 370, and the shape of cross section of the spinneret orifice of spinneret is
Circular.
The modified poly ester that embodiment 1 is obtained is extruded, cools down, oils, is drawn through solid phase polycondensation thickening, metering, porous spinneret
Stretch, thermal finalization and winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion be 280 DEG C, the pathogenic wind-warm of cooling
For 20 DEG C, gr-1 speed 440m/min;80 DEG C of temperature;Gr-2 speed 680m/min;100 DEG C of temperature;Gr-3 speed 2000m/
min;130 DEG C of temperature;Gr-4 speed 2700m/min;240 DEG C of temperature;Gr-5 speed 3000m/min;160 DEG C of temperature;Winding
Speed is 3000m/min.
The fracture strength of prepared high uniformity high-strength polyester industrial fiber is 8.6cn/dtex;Line density deviation ratio is
1%, fracture strength cv value is 1.9%, and extension at break cv value is 5.3%, and extension at break is 12.1, network 7, at 260 DEG C, melts
Body viscosity declines 11%, under the test condition for 177 DEG C × 10min × 0.05cn/dtex for the temperature, the dry-hot shrinkage of fiber
For 8.4%.
When identical with the effective area that embodiment 29 contrast can be seen that spinneret, (circular arrangement when spray webbing hole count is close
Spray webbing hole count is 370, and oval shaped arrangements spray webbing hole count is 374), the spinneret orifice number of plies of oval shaped arrangements is 6, less than circular arrangement
The spinneret orifice number of plies 8, cooling effect is more preferable;When identical with the effective area that embodiment 30 contrast can be seen that spinneret, oval
The spinneret orifice number of plies of shape arrangement is 5, and less than the spinneret orifice number of plies 8 of circular arrangement, cooling effect is more preferable, the spray webbing of oval shaped arrangements
The hole count 382 in hole is more than the hole count 370 of the spinneret orifice of circular arrangement, and cooling effectiveness is higher.The comparing result of fibre property shows,
Fiber linear density deviation ratio that embodiment 29 and embodiment 30 are obtained, fracture strength cv value, extension at break cv value are less than comparative example
1, under the conditions of same process is described, it is better than adopting spinneret using the fibre property that the spinneret of spinneret orifice oval shaped arrangements is obtained
The spinneret of circular arrangement.
Embodiment 31~33
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 310 DEG C, and the pathogenic wind-warm of cooling is 20 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 440m/min;75 DEG C of temperature;Gr-2 speed 460m/min;90 DEG C of temperature;gr-3
Speed 1900m/min;125 DEG C of temperature;Gr-4 speed 2700m/min;220 DEG C of temperature;Gr-5 speed 2500m/min;Temperature 150
℃;The speed of winding is 2600m/min.
At 280 DEG C, melt viscosity declines percent to prepared high uniformity high-strength polyester industrial fiber, industry under room temperature
The mechanical performance data of silk, and temperature be 177 DEG C × 10min × 0.05cn/dtex test condition under, industrial yarn dry
Percent thermal shrinkage such as following table.
Embodiment 34~36
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 310 DEG C, and the pathogenic wind-warm of cooling is 30 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 650m/min;85 DEG C of temperature;Gr-2 speed 680m/min;100 DEG C of temperature;gr-3
Speed 2400m/min;140 DEG C of temperature;Gr-4 speed 3600m/min;250 DEG C of temperature;Gr-5 speed 3600m/min;Temperature 170
℃;The speed of winding is 3600m/min.
Prepared high uniformity high-strength polyester industrial fiber melt viscosity at 290 DEG C declines percentage ratio, industry under room temperature
The mechanical performance data of silk, and temperature be 177 DEG C × 10min × 0.05cn/dtex test condition under, industrial yarn dry
Percent thermal shrinkage such as following table.
Embodiment 37~39
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 290 DEG C, and the pathogenic wind-warm of cooling is 20 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 440m/min;75 DEG C of temperature;Gr-2 speed 460m/min;90 DEG C of temperature;gr-3
Speed 1900m/min;125 DEG C of temperature;Gr-4 speed 2700m/min;220 DEG C of temperature;Gr-5 speed 2500m/min;Temperature 150
℃;The speed of winding is 2600m/min.
Prepared high uniformity high-strength polyester industrial fiber melt viscosity at 270 DEG C declines percent, industry under room temperature
The mechanical performance data of silk, and temperature be 177 DEG C × 10min × 0.05cn/dtex test condition under, industrial yarn dry
Percent thermal shrinkage such as following table.
Embodiment 40~42
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 300 DEG C, and the pathogenic wind-warm of cooling is 25 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 450m/min;80 DEG C of temperature;Gr-2 speed 500m/min;95 DEG C of temperature;gr-3
Speed 2000m/min;130 DEG C of temperature;Gr-4 speed 3000m/min;240 DEG C of temperature;Gr-5 speed 3200m/min;Temperature 160
℃;The speed of winding is 3000m/min.
Prepared high uniformity high-strength polyester industrial fiber melt viscosity at 260 DEG C declines percentage ratio, industry under room temperature
The mechanical performance data of silk, and temperature be 177 DEG C × 10min × 0.05cn/dtex test condition under, industrial yarn dry
Percent thermal shrinkage such as following table.
Embodiment 43~45
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 290 DEG C, and the pathogenic wind-warm of cooling is 30 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 460m/min;85 DEG C of temperature;Gr-2 speed 600m/min;90 DEG C of temperature;gr-3
Speed 2000m/min;130 DEG C of temperature;Gr-4 speed 3600m/min;240 DEG C of temperature;Gr-5 speed 3500m/min;Temperature 150
℃;The speed of winding is 3200m/min.
Prepared high uniformity high-strength polyester industrial fiber at 280 DEG C, melt viscosity, the mechanical property of industrial yarn under room temperature
Energy data, and under the test condition for 177 DEG C × 10min × 0.05cn/dtex for the temperature, the dry-hot shrinkage of industrial yarn is such as
Following table.
Embodiment 46~48
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 310 DEG C, and the pathogenic wind-warm of cooling is 25 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 500m/min;80 DEG C of temperature;Gr-2 speed 580m/min;100 DEG C of temperature;gr-3
Speed 2200m/min;135 DEG C of temperature;Gr-4 speed 3100m/min;230 DEG C of temperature;Gr-5 speed 2800m/min;Temperature 160
℃;The speed of winding is 3000m/min.
Prepared high uniformity high-strength polyester industrial fiber melt viscosity at 280 DEG C declines percent, industry under room temperature
The mechanical performance data of silk, and temperature be 177 DEG C × 10min × 0.05cn/dtex test condition under, industrial yarn dry
Percent thermal shrinkage such as following table.
Embodiment 49~51
A kind of preparation method of high uniformity high-strength polyester industrial fiber.
Spinneret orifice be arranged as long axial symmetry, oval major axis is 1.4 with the ratio of minor axis length, between adjacent spinneret orifice
Add 1.6mm away from the guide hole diameter equal to spinneret orifice, spinneret is circular spinneret, the diameter of circular spinneret is oval with series
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, spray webbing
The shape of cross section of the spinneret orifice of plate is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 310 DEG C, and the pathogenic wind-warm of cooling is 30 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 480m/min;82 DEG C of temperature;Gr-2 speed 580m/min;97 DEG C of temperature;gr-3
Speed 2200m/min;130 DEG C of temperature;Gr-4 speed 3400m/min;230 DEG C of temperature;Gr-5 speed 3100m/min;Temperature 160
℃;The speed of winding is 3300m/min.
Prepared high uniformity high-strength polyester industrial fiber melt viscosity at 280 DEG C, the mechanical property of industrial yarn under room temperature
Energy data, and under the test condition for 177 DEG C × 10min × 0.05cn/dtex for the temperature, the dry-hot shrinkage of industrial yarn is such as
Following table.
Embodiment 52~57
A kind of preparation method of high uniformity high-strength polyester industrial fiber, spinneret orifice be arranged as long axial symmetry, oval
Major axis is 1.4 with the ratio of minor axis length, and the spacing of adjacent spinneret orifice is equal to the guide hole diameter of spinneret orifice plus 1.6mm, spray webbing
Plate is circular spinneret, and the diameter of circular spinneret is 12mm with the difference of the oval maximum long axis length of series, spinneret orifice
The a diameter of 1.5mm of guide hole, the spinneret orifice numerical digit 192 of spinneret, the shape of cross section of the spinneret orifice of spinneret is square.
High uniformity high-strength polyester industrial fiber through metering, porous spinneret extrude, cool down, oiling, stretching, thermal finalization and
Winding, prepared high uniformity high-strength polyester industrial fiber, the wherein temperature of extrusion are 310 DEG C, and the pathogenic wind-warm of cooling is 20 DEG C;Draw
Stretch, heat setting process parameter is: gr-1 speed 440m/min;75~85 DEG C of temperature;Gr-2 speed 680m/min;90 DEG C of temperature;
Gr-3 speed 2400m/min;140 DEG C of temperature;Gr-4 speed 2700m/min;220 DEG C of temperature;Gr-5 speed 3600m/min;Temperature
170 DEG C of degree;The speed of winding is 3000m/min.
Prepared high uniformity high-strength polyester industrial fiber melt viscosity at 280 DEG C declines percentage ratio, industry under room temperature
The mechanical performance data of silk, and temperature be 177 DEG C × 10min × 0.05cn/dtex test condition under, industrial yarn dry
Percent thermal shrinkage such as following table.
Claims (10)
1. a kind of high uniformity high-strength polyester industrial fiber, is characterized in that: described high uniformity high-strength polyester industrial fiber is by changing
Property polyester spinning after solid-phase tack producing obtains;The material of described high uniformity high-strength polyester industrial fiber is modified poly ester, described changes
Property polyester form by p-phthalic acid segment, ethylene glycol segment and containing the dihydroxylic alcohols segment of side chain, the described dihydroxylic alcohols containing side chain
Segment refers to that side chain is located on one of dihydroxylic alcohols segment non-end group carbon and side chain is the straight chain carbon containing 5-10 carbon atom
The dihydroxylic alcohols segment of chain;Fracture strength >=the 8.8cn/dtex of described high uniformity high-strength polyester industrial fiber;Described high uniform
Property high-strength polyester industrial fiber at 260~290 DEG C, melt viscosity decline 10-20%, line density deviation ratio≤1.0%, fracture
Intensity cv value≤2.0%, extension at break cv value≤5.5%.
2. a kind of high uniformity high-strength polyester industrial fiber according to claim 1 is it is characterised in that described high uniformity
The extension at break of high-strength polyester industrial fiber be 12.0 ± 1.5%, network 5 ± 2, temperature be 177 DEG C × 10min ×
Under the test condition of 0.05cn/dtex, the dry-hot shrinkage of fiber is 8.5 ± 1.5%;The number-average molecular weight of described modified poly ester
For 15000-30000.
3. a kind of high uniformity high-strength polyester industrial fiber according to claim 1 it is characterised in that described containing side chain
Dihydroxylic alcohols segment is 2- amyl group -1,3 propylene glycol segment, 2- hexyl -1,3 propylene glycol segment, 2- heptyl -1,3 propylene glycol segment, 2-
Octyl group -1,3 propylene glycol segment, 2- nonyl -1,3 propylene glycol segment, 2- decyl -1,3 propylene glycol segment, 2- amyl group -1,4 butanediol
Segment, 2- hexyl -1,4 butanediol segment, 2- heptyl -1,4 butanediol segment, 2- octyl group -1,4 butanediol segment, 2- nonyl -1,
4 butanediol segments, 2- decyl -1,4 butanediol segment, 2- amyl group -1,5 pentanediol segment, 2- hexyl -1,5 pentanediol segment, 2-
Heptyl -1,5 pentanediol segment, 2- octyl group -1,5 pentanediol segment, 2- nonyl -1,5 pentanediol segment, 2- decyl -1,5 pentanediol
Segment, 2- amyl group -1,6 hexanediol segment, 2- hexyl -1,6 hexanediol segment, 2- heptyl -1,6 hexanediol segment, 2- octyl group -1,
One or more of 6 hexanediol segments, 2- nonyl -1,6 hexanediol segment or 2- decyl -1,6 hexanediol segment;Described containing side chain
The Mole percent ratio of dihydroxylic alcohols segment and ethylene glycol segment be 2~5%.
4. the preparation method of a kind of high uniformity high-strength polyester industrial fiber as any one of claim 1-3, it is special
Levying is: modified poly ester is extruded, cools down, oiling, stretching through solid phase polycondensation thickening, metering, porous spinneret, thermal finalization and volume
Around prepared high uniformity high-strength polyester industrial fiber;
On described porous spinneret, the arrangement mode of spinneret orifice is oval shaped arrangements, and described oval shaped arrangements refer to the hole of spinneret orifice
It is centrally located on concentration ellipse, described concentration ellipse is that series is oval, and all oval major axis are conllinear, and short axle is conllinear;
The preparation process of modified poly ester comprises the following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
P-phthalic acid is made into after slurry with the dihydroxylic alcohols containing side chain, under the catalytic action of concentrated sulphuric acid, carries out esterification,
Obtain p-phthalic acid binary alcohol esters;The described dihydroxylic alcohols containing side chain are that side chain is located at one of dihydroxylic alcohols segment non-end group carbon
Upper and side chain is the dihydroxylic alcohols of the linear carbon chain containing 5-10 carbon atom;
(2) preparation of ethylene glycol terephthalate:
P-phthalic acid and ethylene glycol are made into after slurry, carry out esterification, obtain ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), stirring is mixed
Close, in the presence of catalyst and stabilizer, under conditions of negative pressure, carry out polycondensation reaction and the Gao Zhen in coarse vacuum stage successively
The polycondensation reaction in empty stage, prepared modified poly ester.
5. the preparation method of high uniformity high-strength polyester industrial fiber according to claim 4 is it is characterised in that described change
Property polyester preparation concretely comprise the following steps:
(1) preparation of p-phthalic acid binary alcohol esters:
P-phthalic acid and the dihydroxylic alcohols containing side chain are made into slurry add in reactor, under the catalytic action of concentrated sulphuric acid, enter
Row esterification, esterification compressive reaction in nitrogen atmosphere, moulding pressure is normal pressure~0.3mpa, and temperature is 180~240
DEG C, it is esterification terminal when the water quantity of distillate in esterification reaches more than the 90% of theoretical value;Obtain p-phthalic acid
Binary alcohol esters;
(2) preparation of ethylene glycol terephthalate:
P-phthalic acid and ethylene glycol are made into after slurry and add in reactor, carry out esterification, esterification is in blanket of nitrogen
Enclose middle compressive reaction, moulding pressure is normal pressure~0.3mpa, and temperature is 250~260 DEG C, when the water quantity of distillate in esterification reaches
To theoretical value more than 90% when be esterification terminal, obtain ethylene glycol terephthalate;
(3) preparation of modified poly ester:
After the esterification in step (2) terminates, add the p-phthalic acid binary alcohol esters of preparation in step (1), stirring is mixed
Close 15-20 minute, under conditions of negative pressure, in the presence of catalyst and stabilizer, start the polycondensation reaction in coarse vacuum stage,
This staged pressure is steadily evacuated to below absolute pressure 500pa by normal pressure, temperature control at 260~270 DEG C, the response time be 30~
50 minutes;Then proceed to evacuation, carry out the polycondensation reaction of high vacuum stage of Fig, make reaction pressure be down to absolute pressure and be less than
100pa, reaction temperature controls at 275~280 DEG C, 50~90 minutes response time, prepared modified poly ester;
Again modified poly ester is obtained Modified polyester chips through pelletizing, obtained polyester slice is viscosified by solid phase polycondensation, makes polyester
The intrinsic viscosity of section brings up to 1.0~1.2dl/g, as high viscous section;Again through metering, porous spinneret extrusion, cooling, on
Oil, stretching, thermal finalization and winding, prepared high uniformity high-strength polyester industrial fiber;
Spinning main technologic parameters are:
The temperature of described extrusion is 290~310 DEG C;
The pathogenic wind-warm of described cooling is 20~30 DEG C;
Described stretching, heat setting process parameter are:
Gr-1 speed 440~650m/min;75~85 DEG C of temperature;
Gr-2 speed 460~680m/min;90~100 DEG C of temperature;
Gr-3 speed 1900~2400m/min;125~140 DEG C of temperature;
Gr-4 speed 2700~3600m/min;220~250 DEG C of temperature;
Gr-5 speed 2500~3600m/min;150~170 DEG C of temperature;
The speed of described winding is 2600~3600m/min.
6. a kind of preparation method of high uniformity high-strength polyester industrial fiber according to claim 5 is it is characterised in that institute
State in step (1), p-phthalic acid is 1:1.3-1.5 with the mol ratio of the dihydroxylic alcohols containing side chain;Concentrated sulphuric acid addition is to benzene
The 0.3-0.5% of dioctyl phthalate weight;The concentration of described concentrated sulphuric acid is 50-60wt%;In described step (2), p-phthalic acid with
The mol ratio of ethylene glycol is 1:1.2~2.0;In described step (3), described p-phthalic acid binary alcohol esters and p-phthalic acid second
The Mole percent ratio of diol ester is 2~5%;Described catalyst is antimony oxide, antimony glycol or antimony acetate, and catalyst adds
Enter amount for the 0.01%~0.05% of p-phthalic acid gross weight;Described stabilizer is triphenyl phosphate, trimethyl phosphate or Asia
Trimethyl phosphate, stabilizer addition is the 0.01%~0.05% of described p-phthalic acid gross weight.
7. a kind of preparation method of high uniformity high-strength polyester industrial fiber according to claim 5 is it is characterised in that institute
State dihydroxylic alcohols containing side chain be 2- amyl group -1,3 propylene glycol, 2- hexyl -1,3 propylene glycol, 2- heptyl -1,3 propylene glycol, 2- octyl group -
1,3 propylene glycol, 2- nonyl -1,3 propylene glycol, 2- decyl -1,3 propylene glycol, 2- amyl group -1,4 butanediol, 2- hexyl -1,4 fourth two
Alcohol, 2- heptyl -1,4 butanediol, 2- octyl group -1,4 butanediol, 2- nonyl -1,4 butanediol, 2- decyl -1,4 butanediol, 2- penta
Base -1,5 pentanediol, 2- hexyl -1,5 pentanediol, 2- heptyl -1,5 pentanediol, 2- octyl group -1,5 pentanediol, 2- nonyl -1,5 penta
Glycol, 2- decyl -1,5 pentanediols, 2- amyl group -1,6 hexanediol, 2- hexyl -1,6 hexanediol, 2- heptyl -1,6 hexanediol, 2- are pungent
One or more of base -1,6 hexanediol, 2- nonyl -1,6 hexanediol or 2- decyl -1,6 hexanediol.
8. a kind of preparation method of high uniformity high-strength polyester industrial fiber according to claim 4 is it is characterised in that institute
Stating porous spinneret is circular spinneret or elliptical spinneret plate;The diameter of described circle spinneret oval maximum length with series
The difference of shaft length is more than 10mm, and described elliptical spinneret plate is more than 10mm with the difference of the oval maximum long axis length of series.
9. a kind of preparation method of high uniformity high-strength polyester industrial fiber according to claim 4 is it is characterised in that institute
State spinneret orifice on porous spinneret be arranged as major axis and/or short axle is symmetrical, the spacing of adjacent spinneret orifice is more than or equal to spinneret orifice
Guide hole diameter add 1.5mm;Oval major axis is 1.3~1.8 with the ratio of minor axis length.
10. a kind of high uniformity high-strength polyester industrial fiber according to claim 4 preparation method it is characterised in that
A diameter of 1.5~the 2.5mm of guide hole of described spinneret orifice;The spray webbing hole count of described spinneret is more than or equal to 192, described spinneret
The shape of cross section of spinneret orifice is circle, square, rhombus, yi word pattern, triangular form, trilobal cross, hollow type or platypelloid type.
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CN112779809A (en) * | 2020-12-29 | 2021-05-11 | 江苏恒力化纤股份有限公司 | Papermaking forming net and preparation method thereof |
JP2023553510A (en) * | 2020-12-29 | 2023-12-21 | 江蘇恒力化繊股▲ふん▼有限公司 | Flame-retardant polyester fiber for clothing and its manufacturing method |
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CN112725921A (en) * | 2020-12-29 | 2021-04-30 | 江苏恒力化纤股份有限公司 | High-strength low-elongation polyester industrial yarn and preparation method thereof |
CN112779809A (en) * | 2020-12-29 | 2021-05-11 | 江苏恒力化纤股份有限公司 | Papermaking forming net and preparation method thereof |
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JP2023553509A (en) * | 2020-12-29 | 2023-12-21 | 江蘇恒力化繊股▲ふん▼有限公司 | High strength/thermally stable polyester industrial yarn and its manufacturing method |
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