CN104499091B - A kind of polyester composite filament arranged side by side and preparation method thereof - Google Patents
A kind of polyester composite filament arranged side by side and preparation method thereof Download PDFInfo
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- CN104499091B CN104499091B CN201410852074.8A CN201410852074A CN104499091B CN 104499091 B CN104499091 B CN 104499091B CN 201410852074 A CN201410852074 A CN 201410852074A CN 104499091 B CN104499091 B CN 104499091B
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Abstract
A kind of polyester composite filament arranged side by side, described polyester composite filament arranged side by side is to be obtained by composite spinning arranged side by side by PBT, modified poly ester PET section, described modified poly ester is made up of with amino ethylene glycol fatty acid polyester, described amino ethylene glycol fatty acid is dispersed in the molecule interchain of described polyester, and the molecule interchain of described amino ethylene glycol fatty acid and described polyester has hydrogen bond action, described amino ethylene glycol fatty acid is made to fix with the relative position of the strand of described polyester；Described polyester composite filament arranged side by side polyester is under the conditions of temperature is 90～130 DEG C, and the free volume space of fibrous inside molecule interchain increases 20～30v/v%；Described polyester composite filament arranged side by side, in the case of using the dyestuffs such as Disperse Red 3B, has the dye-uptake more much higher than general fibre, and the loose colour formed after dyeing is less；Described polyester composite filament arranged side by side has broad prospect of application in garment material field.
Description
Technical field
The invention belongs to fibre technology field, relate to a kind of polyester composite filament arranged side by side and preparation method thereof.
Background technology
Polyethylene terephthalate (PET) fiber, since coming out, has obtained rapidly because of the performance of its excellence
Development, its yield has become as the hat of world's synthetic fibers.Polyester fiber has fracture strength and elastic modelling quantity is high, and resilience is fitted
In, thermal finalization is excellent, and heat-resisting light resistance is good and a series of premium properties such as acid-fast alkali-proof corrosion resistance, and fabric has anti-
The advantages such as wrinkle, stiffness are good, so, polyester fiber is widely used in the field such as clothing, home textile.
PET belongs to symmetric straight chain macromolecular, and strand does not contains side-chain radical, and regularity is the best, its main chain
Phenyl ring containing rigidity and flexible alkyl, and the ester group being directly connected with phenyl ring and phenyl ring constitute the conjugated body of rigidity
System, thus constrain rotating freely of its soft segment.This structure is it will be evident that increase on the impact of glass transition temperature
The wall ridge of molecule segment motion, the glass transition temperature of PET is higher, need to dye at very high temperatures, promotes dyestuff
Molecule is to the diffusion of fibrous inside.It addition, the strand of PET is regular, good crystallinity, strand arrangement is tight, and strand
The upper polar group not having an effect with dye molecule, the colouring making polyester fiber is more difficult.
For the problem of solution PET dyeing difficulty, techniques or methods are now used mainly to be connect by introducing dye molecule
By base or the method for increase polyester amorphous regions amount, although the dyeability of polyester can be improved, destroy the segment rule of PET
Whole property, to reduce the performance of polyester fiber to obtain the raising of dyeability.Do not destroying polyester fiber crystallinity and permutation degree
In the case of, the method used at present has three kinds of colouring methods such as support methods, high temperature and high pressure method and high temperature thermosoling.
Polyester composite filament arranged side by side is to utilize the percent thermal shrinkage of PET with PBT both components different, by Compound spinning arranged side by side
Silk, it is thus achieved that have from crimpability, PET/PBT composite bicomponent arranged side by side fiber that superior elasticity can be provided.Due to two component heat
The difference of shrinkage factor be released in last handling process thus create permanent two-dimensional helical curling " shrinkage factor is higher
PBT in the inner side of spiral, the relatively low PET of shrinkage factor is at outside spiral.The difference of two kinds of component shrinkage factors and polymeric inner
Factor (as macromolecular chain chemical composition and structure is different) and external condition (such as stretching, the change of heat set conditions) are relevant.With
Time due to PBT dyeing temperature low compared with PET 10-20 DEG C, the difficulty brought is to select low temperature dyeing, then PET on, dye is inadequate；Select height
Temperature dyeing, then the elasticity of composite filament is impaired.
Summary of the invention
It is an object of the invention to provide a kind of polyester composite filament arranged side by side and preparation method thereof, the present invention utilizes amino fatty acid
Glycol ester is when uniform temperature condition, and the increasing degree of free volume is far longer than the characteristic of polyester macromolecule chain, by carrying
High dispersive dyestuff molecule enters the degree within polyester, improves the dyeability of polyester, the most also can reduce dyeing temperature
Degree reaches Color, reduces the elastic extent of damage of composite filament；Simultaneously because in amino ethylene glycol fatty acid molecule
The existence of the first amino, increases the hydrogen bond action between itself and polyester macromolecule chain, add its compatibility with polyester and
Dispersion in the polyester, decreases migration to greatest extent.Polyester construction regularity, crystallinity are not destroyed simultaneously, keep
The premium properties of polyester.
A kind of polyester composite filament arranged side by side of the present invention, described polyester composite filament arranged side by side is to be cut into slices by PBT, modified poly ester PET
Being obtained by composite spinning arranged side by side, described modified poly ester is to be made up of polyester and amino ethylene glycol fatty acid, described aminolipid
Fat acid glycol ester is dispersed in the molecule interchain of described polyester, and the molecule of described amino ethylene glycol fatty acid and described polyester
Interchain has hydrogen bond action, makes described amino ethylene glycol fatty acid fix with the relative position of the strand of described polyester；Described
Polyester composite filament arranged side by side is under the conditions of temperature is 90～130 DEG C, and the free volume space of fibrous inside molecule interchain increases；
The molecular structure of described amino ethylene glycol fatty acid is:
H2N(CH2)nCOOCH2CH2OOC(CH2)nNH2；
Wherein, n=10-50.
As preferred technical scheme:
Described a kind of polyester composite filament arranged side by side, line density deviation ratio≤0.5% of described polyester composite filament arranged side by side, fracture
Intensity >=3.0cN/dtex, fracture strength CV value≤5.0%, elongation at break is 30.0 ± 3.0%, extension at break CV value≤
10.0%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.
Described a kind of polyester composite filament arranged side by side, described amino ethylene glycol fatty acid accounts for described polyester composite filament arranged side by side
Percentage by weight is 0.5～2.5%.
Present invention also offers the preparation method of a kind of polyester composite filament arranged side by side, it is characterized in that by PBT, modified poly ester PET
Section, respectively through the most threaded, carry out compound distribution at composite component, and extrudes at composite spinneret, cool down, oils, draws
Stretch, thermal finalization and winding, prepare polyester composite filament arranged side by side；
The temperature of described extrusion is 275～285 DEG C；
The pathogenic wind-warm of described cooling is 20～25 DEG C；
The speed of described winding is 4000～4600m/min；
Filament number is 0.7～1.5dtex；
The preparation process of described modified poly ester includes:
(1) preparation of amino ethylene glycol fatty acid:
1) binary of fatty acids is added in reactor with the amount of 1:1.5 mol ratio with methanol, under the catalysis of concentrated sulphuric acid, add
Heat is to 80～110 DEG C, and refuxing esterification, cooling, separating-purifying obtains binary of fatty acids mono-methyl；Described binary of fatty acids is 12
Alkane dicarboxylic acids is to the one in dopentacontane dicarboxylic acids；Reaction equation is:
HOOC(CH2)nCOOH+CH3OH→CH3OOC(CH2)nCOOH
Wherein n=10～50；
2) by described binary of fatty acids mono-methyl, lead tetraacetate and lithium bromide during 1:1:1 is dissolved in benzene in molar ratio, wherein two
The concentration of unit's fatty acid mono-methyl is 0.05～0.1mol/L, and under nitrogen atmosphere, 80～90 DEG C of reactions, backflow, when no longer
When having gas to produce, add a certain amount of dilute sulfuric acid and react 2～3 hours, be washed out, purify and be dried, obtain product bromo
Fatty acid；Reaction equation is:
3), by the ammonia of bromo fatty acid and 15～25wt% during 1:2 joins reactor in molar ratio, stirring, in room temperature
Lower reaction, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is less than 70 DEG C, until nothing
Bubble produces, and i.e. stops distillation, then carries out cooling down and sucking filtration, and filter cake is washed with deionized water to without bromide ion, by product
Vacuum drying obtains product amino fatty acid；Vacuum drying temperature can use 60～70 DEG C；Reaction equation is:
HOOC(CH2)nBr+NH3→HOOC(CH2)nNH2+NH4Br；
4) ethylene glycol and amino fatty acid are stirred for 1.1:2 in molar ratio, and press the hundred of amino fatty acid wt
/ mono-add concentration be 40～50wt% sulphuric acid be catalyst, carry out esterification, esterification reaction temperature is 160～220
DEG C, it is esterification terminal that esterification water quantity of distillate reaches more than the 90% of theoretical value；The separated purification of product obtains amino
Ethylene glycol fatty acid；Reaction equation is:
HOOC(CH2)nNH2+HOCH2CH2OH→
H2N(CH2)nCOOCH2CH2OOC(CH2)nNH2；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
Use p-phthalic acid and ethylene glycol as raw material, after being made into uniform sizing material, carry out esterification, obtain esterification and produce
Thing；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at normal pressure～0.3MPa, and temperature is at 250～260 DEG C, and esterification water evaporates
It is esterification terminal that output reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
In the described polycondensation reaction coarse vacuum stage, esterification products adds catalyst and stabilizer, under conditions of negative pressure
Starting polycondensation reaction, this staged pressure is steadily evacuated to below absolute pressure 500Pa by normal pressure, and temperature controls at 260～270 DEG C,
Response time is 30～50 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino ethylene glycol fatty acid, and stir, generally stir
15～20 minutes；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 275～280 DEG C, response time 50～90 minutes；
Prepare modified poly ester.
The preparation method of a kind of polyester composite filament arranged side by side as above, described ethylene glycol rubs with described p-phthalic acid
Your ratio is 1.2～2.0:1.
The preparation method of a kind of polyester composite filament arranged side by side as above, described catalyst is selected from antimony oxide, second two
One in alcohol antimony and antimony acetate, catalyst amount is the 0.01%～0.05% of described p-phthalic acid weight.
The preparation method of a kind of polyester composite filament arranged side by side as above, described stabilizer is selected from triphenyl phosphate, phosphoric acid
One in trimethyl and NSC 6513, stabilizing agent dosage is the 0.01%～0.05% of described p-phthalic acid weight.
The preparation method of a kind of polyester composite filament arranged side by side as above, is washed with deionized water to without using bromide ion
Silver nitrate solution detects.
The preparation method of a kind of polyester composite filament arranged side by side as above, described concentrated sulphuric acid refer to mass concentration be 70～
The sulphuric acid of 80%, concentrated sulphuric acid addition is the 1～3wt% of binary of fatty acids；Described a certain amount of dilute sulfuric acid refers to mass concentration
Being the sulphuric acid of 40～50%, dilute sulfuric acid addition is the 1～3wt% of binary of fatty acids mono-methyl.
The preparation method of a kind of polyester composite filament arranged side by side as above, it is characterised in that described PBT slicing characteristics sticks
Degree [η]
It is 1.10～1.30dl/g；Described modified poly ester PET slicing characteristics viscosity [η] is 0.64～0.75dl/g；
The preparation method of a kind of polyester composite filament arranged side by side as above, it is characterised in that PBT Yu PET weight in composite filament
The ratio of amount is 4:6～6:4.
Polyester fiber is when dyeing, and disperse dyes can be divided into the following four stage to the upper dye process of polyester fiber:
1) disperse dyes flowing with dye liquor in dye liquor moves closer to fiber interface；2) disperse dyes are near fiber interface
Adsorbed by fiber surface rapidly；3), after disperse dyes are adsorbed to fiber surface, in fiber, a concentration difference or inside and outside is produced
Dyestuff chemistry potential difference, dyestuff will spread to fibrous inside；4) disperse dyes diffusion velocity and fiber unformed area content, hole or
Free volume content is relevant, and therefore the dyeing speed of disperse dyes is in addition to dyestuff dissolubility in the solution, further depends on
When the structure of fiber is outer and dyes, the degree of swelling of fiber is relevant.
Polyster fibre is hydrophobic synthetic fibers, lacks as cellulose or protein fibre in terylene molecular structure
Energy and dyestuff occur combine active group, terylene molecules align must compare closely, only exist less space in fiber,
When dyeing under the conditions of humidity, polyester fiber will not can be by the most swelling and make space increase as cotton fiber, dyestuff divides
Son is difficult to see through fibrous inside.Therefore, raising will assist in the carrying out of dyeing to the free volume between fiber molecule.
The molecular chain structure of polyester is the linear macromolecule containing benzene ring structure, the functional group's marshalling on strand,
Unbranched, macromole chain flexibility is poor.The regularity of polyester is good and rigidity is the biggest simultaneously, and intermolecular active force is bigger.
Compared with other macromolecular materials, the strand generation sliding of polyester, rotation the most more difficulty, these characteristics hinder dyestuff and enter
Enter inside polyester, thus dyeability is poor.
It is main that amino ethylene glycol fatty acid is mainly with C-C, C-O key, has certain molecular weight simultaneously, i.e. has certain
The strand of length, strand flexibility is relatively big, linear big compared with benzene ring structure of the amount of crimp of amino ethylene glycol fatty acid
Molecule is bigger, simultaneously strong compared with the linear macromolecule containing benzene ring structure to the sensitivity of temperature.When the temperature is changed, amino fatty acid
Glycol ester moves prior to the linear macromolecule containing benzene ring structure, and the produced free volume of motion is far longer than containing phenyl ring
Produced by the linear macromolecule of structure.
Added the free volume diffusion with increase dyestuff of polyester fiber by fatty acid ester, improve polyester fiber
Dyeability, make fiber obtain high dye-uptake.
Oxygen in fatty acid ester can form hydrogen bond, but oxygen is when centre position, due to space steric effect and fat
The factors such as the curling of fat acid ester molecules reduce the quantity of itself and the hydrogen evolution hydrogen bond in polyester macromolecule chain；If amino is in α position
On, i.e. amino acids, owing to amino and carbonyl interact, also it is unfavorable for amino and the hydrogen evolution hydrogen in polyester macromolecule chain
Key；When end position at macromole of the amino of amino fatty acid ester, the curling of macromole is little on its impact, adds aminolipid
Amino in fat acid esters and the formation of the hydrogen evolution hydrogen bond in polyester macromolecule chain, improve amino fatty acid ester and polyester simultaneously
Active force between macromolecular chain, decreases sliding and the migration of amino fatty acid ester.
Add amino fatty acid ester and the compatibility of polyester and dispersion in the polyester, decrease to greatest extent and move
Move.Polyester construction regularity, crystallinity are not destroyed simultaneously, maintain the premium properties of polyester.
Beneficial effect:
The polyester composite filament arranged side by side of gained the most of the present invention, owing to amino ethylene glycol fatty acid is based on C-C, has simultaneously
Having certain molecular weight, i.e. have the strand of certain length, strand flexibility is relatively big, and it is compatible that amino adds with polyester
Property.The polyester composite filament arranged side by side of gained is good with the compatibility of amino ethylene glycol fatty acid.
2. due in amino ethylene glycol fatty acid molecule in the existence of the first amino, increase and it and polyester macromolecule chain
Between hydrogen bond action, add its compatibility with polyester and dispersion in the polyester, decrease migration to greatest extent.
The modified poly ester of gained the most of the present invention, owing to the content of amino ethylene glycol fatty acid is less, advises polyester construction
Whole property, crystallinity are not destroyed, and maintain the premium properties of polyester.
4. the amount of crimp of amino ethylene glycol fatty acid is bigger, simultaneously to temperature compared with the linear macromolecule of benzene ring structure
Sensitive strong compared with the linear macromolecule containing benzene ring structure.When the temperature is changed, transport prior to the linear macromolecule containing benzene ring structure
Dynamic, the produced free volume of motion of amino ethylene glycol fatty acid is far longer than the linear macromolecule institute containing benzene ring structure
Produce, increase the diffusion of additive, improve the functional of polyester.
5. fatty acid ester adds the free volume diffusion with increase dyestuff of polyester fiber, by improving dispersion dye
Material molecule enters the degree within polyester, improves the dyeability of polyester, also can reduce dyeing temperature simultaneously and reach
Color, reduces the elastic extent of damage of composite filament；
6. obtain the composite filament arranged side by side that elasticity is excellent, dyeability is excellent.
Detailed description of the invention
Below in conjunction with detailed description of the invention, the present invention is expanded on further.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 that the present invention lectures, art technology
The present invention can be made various changes or modifications by personnel, and these equivalent form of values fall within the application appended claims equally and limited
Fixed scope.
A kind of polyester composite filament arranged side by side of the present invention, described polyester composite filament arranged side by side is to be cut into slices by PBT, modified poly ester PET
Being obtained by composite spinning arranged side by side, described modified poly ester is made up of polyester and amino ethylene glycol fatty acid, described amino fat
Acid glycol ester is dispersed in the molecule interchain of described polyester, and the strand of described amino ethylene glycol fatty acid and described polyester
Between have hydrogen bond action, make described amino ethylene glycol fatty acid fix with the relative position of the strand of described polyester；Described poly-
Ester composite filament arranged side by side under the conditions of temperature is 90～130 DEG C, the free volume space of fibrous inside molecule interchain increase 20～
30v/v%；
The molecular structure of described amino ethylene glycol fatty acid is:
H2N(CH2)nCOOCH2CH2OOC(CH2)nNH2
Wherein, n=10-50.
A kind of polyester composite filament arranged side by side as above, line density deviation ratio≤0.5% of described polyester composite filament arranged side by side,
Fracture strength >=3.0cN/dtex, fracture strength CV value≤5.0%, elongation at break is 30.0 ± 3.0%, extension at break CV value
≤ 10.0%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.
A kind of polyester composite filament arranged side by side as above, described amino ethylene glycol fatty acid accounts for described polyester and is combined side by side
The percentage by weight of silk is 0.5～2.5%.
The preparation method of a kind of polyester composite filament arranged side by side as above, described PBT slicing characteristics viscosity [η] is 1.10
～1.30dl/g；Described modified poly ester PET slicing characteristics viscosity [η] is 0.64～0.75dl/g；
The preparation method of a kind of polyester composite filament arranged side by side as above, in composite filament, the ratio of PBT Yu PET weight is 4:
6～6:4.
Colouring method: dyeing disperse dyes are Disperse Red 3B, the disperse blue SE-2R bright blue S-GL of dispersion, fiber exists respectively
High Temperature High Pressure machine dyes.Before dye, fiber nonionic surfactant processes 30 minutes at 60 DEG C.Dye dosage is 2.0%
(o.w.f)；Dispersant NNO1.2g/L, pH value is 5, and bath raio is 1:50,60 DEG C of people dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C,
120 DEG C of each constant temperature dyeing 1h.
Dye uptake uses residual liquid colorimetry to determine, draws appropriate dyeing stock solution and dyeing residual liquid, adds N, N-2 first
Base Methanamide (DMF) and distilled water, be that the ratio of the DMF in dye liquor to be measured and water is 70/30 (v/v), and dye liquor absorbance uses
Ultraviolet-visible spectrophotometer measures, and calculates dye uptake with following formula.
In above formula, A0 and A1 is respectively dyeing stock solution and the absorbance of dyeing residual liquid.
Embodiment 1
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) dodecanedicarboxylic acid is added in reactor with methanol with the amount of 1:1.5 mol ratio, under the catalysis of concentrated sulphuric acid,
Being heated to 80 DEG C, refuxing esterification, cooling, separating-purifying obtains dodecanedicarboxylic acid mono-methyl；Described concentrated sulphuric acid refers to that quality is dense
Degree is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 3wt% of dodecanedicarboxylic acid；
2) described dodecanedicarboxylic acid mono-methyl, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), wherein
Dodecanedicarboxylic acid mono-methyl concentration is 0.05mol/L, under nitrogen atmosphere, in 80 DEG C of reactions, backflow, produces when no longer there being gas
Time raw, add a certain amount of dilute sulfuric acid and react 2 hours, be washed out, purify and be dried, obtain product bromoundecane carboxylic acid；
Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 40%, and dilute sulfuric acid addition is dodecanedicarboxylic acid mono-methyl
3wt%；
3), by the ammonia of bromoundecane carboxylic acid Yu 15wt% during 1:2 joins reactor in molar ratio, stirring, in room temperature
Lower reaction, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 60 DEG C, until bubble-free
Producing, i.e. stop distillation, then carry out cooling down and sucking filtration, filter cake is washed with deionized water to without bromide ion, uses silver nitrate
Solution detects, and product vacuum drying is obtained product amino-undecanoic carboxylic acid；
4) ethylene glycol and amino-undecanoic carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino-undecanoic carboxylic acid
1% addition concentration of weight is the sulphuric acid of 40wt%, carries out esterification, and esterification reaction temperature is 160 DEG C, esterification water quantity of distillate
Reaching more than the 90% of theoretical value is esterification terminal；The separated purification of product obtains amino-undecanoic carboxylic acid ethylene glycol
Ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:1.2 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.3MPa, and temperature is 250 DEG C, esterification
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, three oxidations of the 0.01% of addition p-phthalic acid weight in esterification products
Two antimony and the triphenyl phosphate of p-phthalic acid weight 0.01%, start polycondensation reaction, this staged pressure under conditions of negative pressure
Steadily be evacuated to below absolute pressure 500Pa by normal pressure, temperature controls at 260 DEG C, and the response time is 50 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino-undecanoic carboxylic acid glycol ester, and stir 15 points
Clock；Described amino-undecanoic carboxylic acid glycol ester, addition is the 0.5wt% of modified poly ester；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 275 DEG C, 90 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 15000；Described modified poly ester is under the conditions of temperature is 90 DEG C, in polyester
The free volume space of parton interchain increases 20v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 4:6 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 275 DEG C；
The pathogenic wind-warm of described cooling is 20 DEG C；
The speed of described winding is 4300m/min；
Filament number is 1.0dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.2cN/dtex, fracture strength CV value 4.8%, elongation at break is 30.0%, extension at break CV
Value 9.8%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester
Composite filament dyes side by side, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 68.3 | 83.9 | 93.7 | 93.8 | 94.1 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 |
| Disperse blue SE-2R | Modified fibre | 76.5 | 88.9 | 94.2 | 95.4 | 96.7 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 67.5 | 88.8 | 93.6 | 94.1 | 96.7 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 2
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) dopentacontane dicarboxylic acids is added in reactor with methanol with the amount of 1:1.5 mol ratio, in the catalysis of concentrated sulphuric acid
Under, it being heated to 110 DEG C, refuxing esterification, cooling, separating-purifying obtains dopentacontane mono methyl dicarboxylate；Described concentrated sulphuric acid refers to
Mass concentration is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 3wt% of dopentacontane dicarboxylic acids；
2) described dopentacontane mono methyl dicarboxylate, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), its
Middle dopentacontane mono methyl dicarboxylate's concentration is 0.07mol/L, and under nitrogen atmosphere, 85 DEG C of reactions, backflow, when no longer there being gas
When body produces, add a certain amount of dilute sulfuric acid and react 3 hours, be washed out, purify and be dried, obtain product bromo henpentacontane
Carboxylic acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 40%, and dilute sulfuric acid addition is dopentacontane dicarboxylic acids
The 3wt% of mono-methyl；
3), by the ammonia of bromo henpentacontane carboxylic acid Yu 25wt% during 1:2 joins reactor in molar ratio, stirring, in room
The lower reaction of temperature, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 62 DEG C, until depletion of QI
Bubble produces, and i.e. stops distillation, then carries out cooling down and sucking filtration, and filter cake is washed with deionized water to without bromide ion, uses nitric acid
Silver solution detection, obtains product amino henpentacontane carboxylic acid by product vacuum drying；
4) ethylene glycol and amino henpentacontane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino henpentacontane
2% addition concentration of carboxylic acid weight is the sulphuric acid of 45wt%, carries out esterification, and esterification reaction temperature is 220 DEG C, and esterification water evaporates
It is esterification terminal that output reaches more than the 90% of theoretical value；The separated purification of product obtains amino henpentacontane carboxylic acid
Glycol ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:2.0 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.2MPa, and temperature, at 260 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, three oxidations of the 0.05% of addition p-phthalic acid weight in esterification products
Two antimony and right
The triphenyl phosphate of phthalic acid weight 0.05%, starts polycondensation reaction, this staged pressure under conditions of negative pressure
Steadily be evacuated to below absolute pressure 500Pa by normal pressure, temperature controls at 270 DEG C, and the response time is 30 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino henpentacontane carboxylic acid glycol ester, and stir 20 points
Clock；Described amino henpentacontane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 2.5%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 280 DEG C, 50 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 30000；Described modified poly ester is under the conditions of temperature is 130 DEG C, in polyester
The free volume space of parton interchain increases 30v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 5:5 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 285 DEG C；
The pathogenic wind-warm of described cooling is 25 DEG C；
The speed of described winding is 4600m/min；
Filament number is 0.7dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.4cN/dtex, fracture strength CV value 4.5%, elongation at break is 28.0%, extension at break CV
Value 9.6%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester
Composite filament dyes side by side, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 69.5 | 85.9 | 94.1 | 94.2 | 95.1 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 77.5 | 90.2 | 95.3 | 96.8 | 97.0 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 68.9 | 89.8 | 94.0 | 95.2 | 97.1 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 3
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) pentacosane dicarboxylic acid is added in reactor with methanol with the amount of 1:1.5 mol ratio, under the catalysis of concentrated sulphuric acid,
Being heated to 85 DEG C, refuxing esterification, cooling, separating-purifying obtains pentacosane dicarboxylic acid mono-methyl；Described concentrated sulphuric acid refers to that quality is dense
Degree is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 3wt% of pentacosane dicarboxylic acid；
2) described pentacosane dicarboxylic acid mono-methyl, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), wherein
Pentacosane dicarboxylic acid mono-methyl concentration is 0.08mol/L, under nitrogen atmosphere, in 90 DEG C of reactions, backflow, produces when no longer there being gas
Time raw, add a certain amount of dilute sulfuric acid and react 2.5 hours, be washed out, purify and be dried, obtain product bromotetradecane carboxylic
Acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 50%, and dilute sulfuric acid addition is pentacosane dicarboxylic acid list first
The 3wt% of ester；
3), by the ammonia of bromotetradecane carboxylic acid Yu 20wt% during 1:2 joins reactor in molar ratio, stirring, in room temperature
Lower reaction, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 60 DEG C, until bubble-free
Producing, i.e. stop distillation, then carry out cooling down and sucking filtration, filter cake is washed with deionized water to without bromide ion, uses silver nitrate
Solution detects, and product vacuum drying is obtained product amino tetradecane carboxylic acid；
4) ethylene glycol and amino tetradecane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino tetradecane carboxylic acid
2% addition concentration of weight is the sulphuric acid of 50wt%, carries out esterification, and esterification reaction temperature is 190 DEG C, esterification water quantity of distillate
Reaching more than the 90% of theoretical value is esterification terminal；The separated purification of product obtains amino tetradecane carboxylic acid ethylene glycol
Ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:1.6 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.3MPa, and temperature, at 255 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, three oxidations of the 0.03% of addition p-phthalic acid weight in esterification products
Two antimony and the triphenyl phosphate of p-phthalic acid weight 0.03%, start polycondensation reaction, this staged pressure under conditions of negative pressure
Steadily be evacuated to below absolute pressure 500Pa by normal pressure, temperature controls at 265 DEG C, and the response time is 40 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino tetradecane carboxylic acid glycol ester, and stir 16 points
Clock；Described amino tetradecane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 1.0%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 276 DEG C, 70 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 22500；Described modified poly ester is under the conditions of temperature is 100 DEG C, in polyester
The free volume space of parton interchain increases 21v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 6:4 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 280 DEG C；
The pathogenic wind-warm of described cooling is 250 DEG C；
The speed of described winding is 4300m/min；
Filament number is 1.1dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.5%, fracture strength 3.1cN/dtex, fracture strength CV value 4.6%, elongation at break is 30.5%, extension at break CV
Value 9.7%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester
Composite filament dyes side by side, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 67.6 | 82.1 | 91.9 | 92.6 | 93.5 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 75.6 | 87.3 | 93.2 | 94.5 | 95.5 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 66.2 | 87.3 | 91.9 | 93.9 | 95.7 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 4
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) eicosane dicarboxylic acids is added in reactor with methanol with the amount of 1:1.5 mol ratio, under the catalysis of concentrated sulphuric acid,
Being heated to 85 DEG C, refuxing esterification, cooling, separating-purifying obtains eicosane mono methyl dicarboxylate；Described concentrated sulphuric acid refers to that quality is dense
Degree is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 3wt% of eicosane dicarboxylic acids；
2) described eicosane mono methyl dicarboxylate, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), wherein
Eicosane mono methyl dicarboxylate's concentration is 0.09mol/L, under nitrogen atmosphere, in 80 DEG C of reactions, backflow, produces when no longer there being gas
Time raw, add a certain amount of dilute sulfuric acid and react 2.1 hours, be washed out, purify and be dried, obtain product bromo nonadecane carboxylic
Acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 43%, and dilute sulfuric acid addition is eicosane dicarboxylic acids list first
The 2wt% of ester；
3), by the ammonia of bromo nonadecane carboxylic acid Yu 16wt% during 1:2 joins reactor in molar ratio, stirring, in room temperature
Lower reaction, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 69 DEG C, until bubble-free
Producing, i.e. stop distillation, then carry out cooling down and sucking filtration, filter cake is washed with deionized water to without bromide ion, uses silver nitrate
Solution detects, and product vacuum drying is obtained product amino nonadecane carboxylic acid；
4) ethylene glycol and amino nonadecane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino nonadecane carboxylic acid
2% addition concentration of weight is the sulphuric acid of 42wt%, carries out esterification, and esterification reaction temperature is 160 DEG C, esterification water quantity of distillate
Reaching more than the 90% of theoretical value is esterification terminal；The separated purification of product obtains amino nonadecane carboxylic acid ethylene glycol
Ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:1.2 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.15MPa, and temperature, at 251 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, three oxidations of the 0.02% of addition p-phthalic acid weight in esterification products
Two antimony and the triphenyl phosphate of p-phthalic acid weight 0.02%, start polycondensation reaction, this staged pressure under conditions of negative pressure
Steadily be evacuated to below absolute pressure 500Pa by normal pressure, temperature controls at 262 DEG C, and the response time is 33 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino nonadecane carboxylic acid glycol ester, and stir 17 points
Clock；Described amino nonadecane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 1.5%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 277 DEG C, 55 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 16000；Described modified poly ester is under the conditions of temperature is 105 DEG C, in polyester
The free volume space of parton interchain increases 22v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 4:6 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 280 DEG C；
The pathogenic wind-warm of described cooling is 20 DEG C；
The speed of described winding is 4200m/min；
Filament number is 0.9dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.1cN/dtex, fracture strength CV value 4.7%, elongation at break is 29.5%, extension at break CV
Value 9.6%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 68.9 | 85.6 | 94.7 | 94.1 | 94.3 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 77.5 | 89.9 | 94.9 | 95.6 | 96.9 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 67.6 | 88.9 | 93.9 | 94.8 | 96.7 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 5
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) melissane dicarboxylic acids is added in reactor with methanol with the amount of 1:1.5 mol ratio, under the catalysis of concentrated sulphuric acid,
Being heated to 90 DEG C, refuxing esterification, cooling, separating-purifying obtains melissane mono methyl dicarboxylate；Described concentrated sulphuric acid refers to that quality is dense
Degree is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 3wt% of melissane dicarboxylic acids；
2) described melissane mono methyl dicarboxylate, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), wherein
Melissane mono methyl dicarboxylate's concentration be 0.10mol/L under nitrogen atmosphere, 85 DEG C of reactions, backflow, produce when no longer there being gas
Time raw, add a certain amount of dilute sulfuric acid and react 2.3 hours, be washed out, purify and be dried, obtain product bromo nonacosane carboxylic
Acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 40%, and dilute sulfuric acid addition is melissane dicarboxylic acids list first
The 3wt% of ester；
3), by the ammonia of bromo nonacosane carboxylic acid Yu 18wt% during 1:2 joins reactor in molar ratio, stirring, in room
The lower reaction of temperature, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 67 DEG C, until depletion of QI
Bubble produces, and i.e. stops distillation, then carries out cooling down and sucking filtration, and filter cake is washed with deionized water to without bromide ion, uses nitric acid
Silver solution detection, obtains product amino nonacosane carboxylic acid by product vacuum drying；
4) ethylene glycol and amino nonacosane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino nonacosane
2% addition concentration of carboxylic acid weight is the sulphuric acid of 48wt%, carries out esterification, and esterification reaction temperature is 170 DEG C, and esterification water evaporates
It is esterification terminal that output reaches more than the 90% of theoretical value；The separated purification of product obtains amino nonacosane carboxylic acid
Glycol ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:1.5 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.3MPa, and temperature, at 254 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, the ethylene glycol of the 0.01% of addition p-phthalic acid weight in esterification products
Antimony and the trimethyl phosphate of p-phthalic acid weight 0.03%, under conditions of negative pressure start polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to below absolute pressure 500Pa, and temperature controls at 266 DEG C, and the response time is 39 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino nonacosane carboxylic acid glycol ester, and stir 18 points
Clock；Described amino nonacosane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 2.5%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 278 DEG C, 60 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 22000；Described modified poly ester is under the conditions of temperature is 115 DEG C, in polyester
The free volume space of parton interchain increases 23v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 4:6 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 275 DEG C；
The pathogenic wind-warm of described cooling is 20 DEG C；
The speed of described winding is 4300m/min；
Filament number is 1.0dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.2cN/dtex, fracture strength CV value 4.8%, elongation at break is 30.0%, extension at break CV
Value 9.8%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester
Composite filament dyes side by side, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 69.2 | 84.5 | 93.8 | 93.9 | 94.1 |
| General fibre | 66.7 | 78.8 | 83.7 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 77.6 | 89.5 | 94.8 | 95.4 | 96.8 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 67.4 | 89.7 | 93.7 | 94.2 | 96.8 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 6
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) pentatriacontane dicarboxylic acids is added in reactor with methanol with the amount of 1:1.5 mol ratio, in the catalysis of concentrated sulphuric acid
Under, it being heated to 95 DEG C, refuxing esterification, cooling, separating-purifying obtains pentatriacontane mono methyl dicarboxylate；Described concentrated sulphuric acid refers to matter
Amount concentration is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 2wt% of pentatriacontane dicarboxylic acids；
2) described pentatriacontane mono methyl dicarboxylate, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), its
Middle pentatriacontane mono methyl dicarboxylate's concentration be 0.09mol/L under nitrogen atmosphere, 90 DEG C of reactions, backflow, when no longer there being gas
When body produces, add a certain amount of dilute sulfuric acid and react 2.6 hours, be washed out, purify and be dried, obtain product bromo 34
Alkane carboxylic acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 45%, and dilute sulfuric acid addition is pentatriacontane dicarboxyl
The 1wt% of acid mono-methyl
3), by the ammonia of bromo tetratriacontane carboxylic acid Yu 20wt% during 1:2 joins reactor in molar ratio, stirring, in room
The lower reaction of temperature, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 69 DEG C, until depletion of QI
Bubble produces, and i.e. stops distillation, then carries out cooling down and sucking filtration, and filter cake is washed with deionized water to without bromide ion, uses nitric acid
Silver solution detection, obtains product amino tetratriacontane carboxylic acid by product vacuum drying；
4) ethylene glycol and amino tetratriacontane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino tetratriacontane
1% addition concentration of carboxylic acid weight is the sulphuric acid of 50wt%, carries out esterification, and esterification reaction temperature is 180 DEG C, and esterification water evaporates
It is esterification terminal that output reaches more than the 90% of theoretical value；The separated purification of product obtains amino tetratriacontane carboxylic acid
Glycol ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:1.6 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.4MPa, and temperature, at 256 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, the antimony acetate of the 0.04% of addition p-phthalic acid weight in esterification products
With the NSC 6513 of p-phthalic acid weight 0.02%, under conditions of negative pressure start polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to below absolute pressure 500Pa, and temperature controls at 267 DEG C, and the response time is 40 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino tetratriacontane carboxylic acid glycol ester, and stir 18 points
Clock；Described amino tetratriacontane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 2.0%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 275 DEG C, 70 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 24000；Described modified poly ester is under the conditions of temperature is 120 DEG C, in polyester
The free volume space of parton interchain increases 25v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 4:6 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 275 DEG C；
The pathogenic wind-warm of described cooling is 20 DEG C；
The speed of described winding is 4300m/min；
Filament number is 1.0dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.2cN/dtex, fracture strength CV value 4.8%, elongation at break is 30.0%, extension at break CV
Value 9.8%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester
Composite filament dyes side by side, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 68.3 | 83.3 | 93.5 | 93.4 | 94.1 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 76.1 | 88.5 | 94.3 | 95.2 | 96.5 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 67.3 | 88.3 | 93.2 | 94.0 | 96.4 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 7
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) tetracontane dicarboxylic acids is added in reactor with methanol with the amount of 1:1.5 mol ratio, under the catalysis of concentrated sulphuric acid,
Being heated to 100 DEG C, refuxing esterification, cooling, separating-purifying obtains tetracontane mono methyl dicarboxylate；Described concentrated sulphuric acid refers to that quality is dense
Degree is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 3wt% of tetracontane dicarboxylic acids；
2) described tetracontane mono methyl dicarboxylate, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), wherein
Tetracontane mono methyl dicarboxylate's concentration be 0.06mol/L under nitrogen atmosphere, 80 DEG C of reactions, backflow, produce when no longer there being gas
Time raw, add a certain amount of dilute sulfuric acid and react 2.7 hours, be washed out, purify and be dried, obtain product bromo nonatriacontane carboxylic
Acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 48%, and dilute sulfuric acid addition is tetracontane dicarboxylic acids list first
The 2wt% of ester；
3), by the ammonia of bromo nonatriacontane carboxylic acid Yu 22wt% during 1:2 joins reactor in molar ratio, stirring, in room
The lower reaction of temperature, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is 60 DEG C, until depletion of QI
Bubble produces, and i.e. stops distillation, then carries out cooling down and sucking filtration, and filter cake is washed with deionized water to without bromide ion, uses nitric acid
Silver solution detection, obtains product amino nonatriacontane carboxylic acid by product vacuum drying；
4) ethylene glycol and amino nonatriacontane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino nonatriacontane
2% addition concentration of carboxylic acid weight is the sulphuric acid of 46wt%, carries out esterification, and esterification reaction temperature is 190 DEG C, and esterification water evaporates
It is esterification terminal that output reaches more than the 90% of theoretical value；The separated purification of product obtains amino nonatriacontane carboxylic acid
Glycol ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:1.8 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.2MPa, and temperature, at 258 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, the antimony acetate of the 0.05% of addition p-phthalic acid weight in esterification products
With the trimethyl phosphate of p-phthalic acid weight 0.03%, starting polycondensation reaction under conditions of negative pressure, this staged pressure is by often
Flattening and be surely evacuated to below absolute pressure 500Pa, temperature controls at 268 DEG C, and the response time is 45 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino nonatriacontane carboxylic acid glycol ester, and stir 16 points
Clock；Described amino nonatriacontane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 1.5%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power is down to absolute pressure and is less than 100Pa, and reaction temperature controls at 275 DEG C, 75 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 25000；Described modified poly ester is under the conditions of temperature is 128 DEG C, in polyester
The free volume space of parton interchain increases 27v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 5:5 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 275 DEG C；
The pathogenic wind-warm of described cooling is 20 DEG C；
The speed of described winding is 4300m/min；
Filament number is 1.0dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.2cN/dtex, fracture strength CV value 4.6%, elongation at break is 29%, extension at break CV value
9.6%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester also
Row composite filament dyes, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 68.4 | 84.1 | 93.9 | 93.9 | 94.1 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 76.7 | 89.1 | 94.8 | 95.4 | 96.8 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 67.8 | 88.4 | 93.7 | 94.2 | 96.7 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Embodiment 8
The preparation method of a kind of polyester composite filament arranged side by side, comprises the following steps:
(1) preparation of amino ethylene glycol fatty acid:
1) pentatetracontane dicarboxylic acids is added in reactor with methanol with the amount of 1:1.5 mol ratio, in the catalysis of concentrated sulphuric acid
Under, it being heated to 110 DEG C, refuxing esterification, cooling, separating-purifying obtains pentatetracontane mono methyl dicarboxylate；Described concentrated sulphuric acid refers to
Mass concentration is the sulphuric acid of 70%, and concentrated sulphuric acid addition is the 2wt% of pentatetracontane dicarboxylic acids；
2) described pentatetracontane mono methyl dicarboxylate, lead tetraacetate and lithium bromide are dissolved in benzene (mol ratio 1:1:1), its
Middle pentatetracontane mono methyl dicarboxylate's concentration is 0.07mol/L, and under nitrogen atmosphere, 88 DEG C of reactions, backflow, when no longer there being gas
When body produces, add a certain amount of dilute sulfuric acid and react 2.3 hours, be washed out, purify and be dried, obtain product bromo 44
Alkane carboxylic acid；Described a certain amount of dilute sulfuric acid refers to the sulphuric acid that mass concentration is 45%, and dilute sulfuric acid addition is pentatetracontane dicarboxyl
The 2wt% of acid mono-methyl；
3), by the ammonia of bromo tetratetracontane carboxylic acid Yu 25wt% during 1:2 joins reactor in molar ratio, stirring, in room
The lower reaction of temperature, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is less than 70 DEG C, until
Bubble-free produces, and i.e. stops distillation, then carries out cooling down and sucking filtration, and filter cake is washed with deionized water to without bromide ion, uses
Silver nitrate solution detects, and product vacuum drying is obtained product amino tetratetracontane carboxylic acid；
4) ethylene glycol and amino tetratetracontane carboxylic acid are stirred for 1.1:2 in molar ratio, and press amino tetratetracontane
1% addition concentration of carboxylic acid weight is the sulphuric acid of 50wt%, carries out esterification, and esterification reaction temperature is 210 DEG C, and esterification water evaporates
It is esterification terminal that output reaches more than the 90% of theoretical value；The separated purification of product obtains amino tetratetracontane carboxylic acid
Glycol ester；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
The p-phthalic acid using mol ratio to be 1:2.0 and ethylene glycol, as raw material, are esterified after being made into uniform sizing material
Reaction, obtains esterification products；Esterification is pressurizeed in nitrogen atmosphere, and Stress control is at 0.3MPa, and temperature, at 260 DEG C, is esterified
It is esterification terminal that water quantity of distillate reaches more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
The described polycondensation reaction coarse vacuum stage, the ethylene glycol of the 0.02% of addition p-phthalic acid weight in esterification products
Antimony and the trimethyl phosphate of p-phthalic acid weight 0.05%, under conditions of negative pressure start polycondensation reaction, this staged pressure by
Normal pressure is steadily evacuated to below absolute pressure 500Pa, and temperature controls at 270 DEG C, and the response time is 50 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino tetratetracontane carboxylic acid glycol ester, and stir 20 points
Clock；Described amino tetratetracontane carboxylic acid glycol ester addition be the percentage by weight of modified poly ester be 2.0%；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure
Power drops
To absolute pressure less than 100Pa, reaction temperature controls at 280 DEG C, 85 minutes response time；
Preparing modified poly ester, viscosity-average molecular weight is 30000；Described modified poly ester is under the conditions of temperature is 128 DEG C, in polyester
The free volume space of parton interchain increases 29v/v%.
(3) preparation of polyester composite filament arranged side by side
PBT, modified poly ester PET are cut into slices respectively through the most threaded, at composite component, carries out compound distribution, wherein PBT
Be 5:5 with the ratio of PET weight, and extrude at composite spinneret, cool down, oil, stretch, thermal finalization and winding, prepare polyester
Composite filament side by side；
The temperature of described extrusion is 275 DEG C；
The pathogenic wind-warm of described cooling is 20 DEG C；
The speed of described winding is 4300m/min；
Filament number is 1.0dtex；
A kind of polyester composite filament arranged side by side as above, it is characterised in that the line density of described polyester composite filament arranged side by side is inclined
Rate 0.4%, fracture strength 3.2cN/dtex, fracture strength CV value 4.6%, elongation at break is 29%, extension at break CV value
9.6%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content 1.00 ± 0.20%.By polyester also
Row composite filament dyes, and its dye-uptake is as follows:
The dye uptake (%) of fiber
| Dyestuff | Temperature | 90℃ | 100℃ | 110℃ | 120℃ | 130℃ |
| Disperse Red 3B | Modified fibre | 69.4 | 84.1 | 93.9 | 93.9 | 94.1 |
| General fibre | 66.7 | 78.8 | 83.6 | 91.4 | 92.3 | |
| Disperse blue SE-2R | Modified fibre | 76.7 | 89.1 | 94.8 | 95.4 | 96.8 |
| General fibre | 62.6 | 76.2 | 83.7 | 91.2 | 92.5 | |
| Disperse bright blue S-GL | Modified fibre | 67.8 | 88.4 | 93.7 | 94.2 | 96.6 |
| General fibre | 58.7 | 77.3 | 87.7 | 91.6 | 92.8 |
Claims (9)
1. a polyester composite filament arranged side by side, is characterized in that: described polyester composite filament arranged side by side is to be passed through by PBT and Modified polyester chips
Side by side composite spinning and obtain, described modified poly ester is made up of polyester and amino ethylene glycol fatty acid, described amino fatty acid second
Diol ester is dispersed in the molecule interchain of described polyester, and the molecule interchain of described amino ethylene glycol fatty acid and described polyester has
Hydrogen bond action, makes described amino ethylene glycol fatty acid fix with the relative position of the strand of described polyester；Described polyester is also
Row composite filament polyester under the conditions of temperature is 90～130 DEG C, the free volume space of fibrous inside molecule interchain increase 20～
30v/v%；
The molecular structure of described amino ethylene glycol fatty acid is:
H2N(CH2)nCOOCH2CH2OOC(CH2)n NH2；
Wherein, n=10-50；It is 0.5 that described amino ethylene glycol fatty acid accounts for the percentage by weight of described polyester composite filament arranged side by side
～2.5%.
A kind of polyester composite filament arranged side by side the most according to claim 1, it is characterised in that the line of described polyester composite filament arranged side by side
Density variation rate≤0.5%, fracture strength >=3.0cN/dtex, fracture strength CV value≤5.0%, elongation at break is 30.0 ±
3.0%, extension at break CV value≤10.0%, yarn unevenness CV≤2.00%, boiling water shrinkage 10.0 ± 0.5%, oil content
1.00 ± 0.20%.
The preparation method of a kind of polyester composite filament arranged side by side the most as claimed in claim 1, is characterized in that: by PBT and modified poly ester
Section, respectively through the most threaded, carry out compound distribution at composite component, and extrudes at composite spinneret, cool down, oils, draws
Stretch, thermal finalization and winding, prepare polyester composite filament arranged side by side；
The temperature of described extrusion is 275～285 DEG C；
The pathogenic wind-warm of described cooling is 20～25 DEG C；
The speed of described winding is 4000～4600m/min；
Filament number is 0.7～1.5dtex；
The preparation process of described modified poly ester includes:
(1) preparation of amino ethylene glycol fatty acid:
1) binary of fatty acids is added in reactor with the amount of 1:1.5 mol ratio with methanol, under the catalysis of concentrated sulphuric acid, be heated to
80～110 DEG C, refuxing esterification, cooling, separating-purifying obtains binary of fatty acids mono-methyl；Described binary of fatty acids is dodecane two
Carboxylic acid is to the one in dopentacontane dicarboxylic acids；
2) by described binary of fatty acids mono-methyl, lead tetraacetate and lithium bromide during 1:1:1 is dissolved in benzene in molar ratio, wherein binary fat
The concentration of fat acid mono-methyl is 0.05～0.1mol/L, and under nitrogen atmosphere, 80～90 DEG C of reactions, backflow, when no longer there being gas
When body produces, add a certain amount of dilute sulfuric acid and react 2～3 hours, be washed out, purify and be dried, obtain product bromo fat
Acid；
3) by the ammonia of bromo fatty acid and 15～25wt% during 1:2 joins reactor in molar ratio, stirring, the most instead
Should, then product is added thermal distillation, and absorb ammonia with cold water, the temperature adding thermal distillation is less than 70 DEG C, until bubble-free
Producing, i.e. stop distillation, then carry out cooling down and sucking filtration, filter cake is washed with deionized water to without bromide ion, by product vacuum
It is dried to obtain product amino fatty acid；
4) ethylene glycol and amino fatty acid are stirred for 1.1:2 in molar ratio, and press the 1～3% of amino fatty acid wt
Adding the sulphuric acid that concentration is 40～50wt%, carry out esterification, esterification reaction temperature is 160～220 DEG C, esterification water quantity of distillate
Reaching more than the 90% of theoretical value is esterification terminal；The separated purification of product obtains amino ethylene glycol fatty acid；
(2) preparation of modified poly ester, including esterification and polycondensation reaction:
Described esterification:
Use p-phthalic acid and ethylene glycol as raw material, carry out esterification after being made into uniform sizing material, obtain esterification products；Ester
Changing reaction to pressurize in nitrogen atmosphere, Stress control is at normal pressure～0.3MPa, and temperature is at 250～260 DEG C, and esterification water quantity of distillate reaches
It is esterification terminal to more than the 90% of theoretical value；
Described polycondensation reaction:
Including polycondensation reaction coarse vacuum stage and polycondensation reaction high vacuum stage of Fig:
In the described polycondensation reaction coarse vacuum stage, esterification products adds catalyst and stabilizer, starts under conditions of negative pressure
Polycondensation reaction, this staged pressure is steadily evacuated to below absolute pressure 500Pa by normal pressure, and temperature controls at 260～270 DEG C, reaction
Time is 30～50 minutes；
After the described polycondensation reaction coarse vacuum stage terminates, add amino ethylene glycol fatty acid, and stir；
Described polycondensation reaction high vacuum stage of Fig, after the described polycondensation reaction coarse vacuum stage, continues evacuation, makes reaction pressure drop
To absolute pressure less than 100Pa, reaction temperature controls at 275～280 DEG C, response time 50～90 minutes；
Prepare modified poly ester.
The preparation method of a kind of polyester composite filament arranged side by side the most according to claim 3, it is characterised in that described ethylene glycol with
The mol ratio of described p-phthalic acid is 1.2～2.0:1.
The preparation method of a kind of polyester composite filament arranged side by side the most according to claim 3, it is characterised in that described catalyst selects
One in antimony oxide, antimony glycol and antimony acetate, catalyst amount is the 0.01% of described p-phthalic acid weight
～0.05%；Described stabilizer one in triphenyl phosphate, trimethyl phosphate and NSC 6513, stabilizing agent dosage
For described p-phthalic acid weight 0.01%～0.05%.
The preparation method of a kind of polyester composite filament arranged side by side the most according to claim 3, it is characterised in that add amino fat
Stirring after acid glycol ester, the time is 15～20 minutes.
The preparation method of a kind of polyester composite filament arranged side by side the most according to claim 3, it is characterised in that described PBT cuts
Sheet intrinsic viscosity [η] is 1.10～1.30dL/g；Described modified poly ester PET slicing characteristics viscosity [η] is 0.64～0.75dL/
g。
The preparation method of a kind of polyester composite filament arranged side by side the most according to claim 3, it is characterised in that described concentrated sulphuric acid is
Referring to the sulphuric acid that mass concentration is 70～80%, concentrated sulphuric acid addition is the 1～3wt% of binary of fatty acids；Described a certain amount of dilute
Sulphuric acid refers to the sulphuric acid that mass concentration is 40～50%, and dilute sulfuric acid addition is the 1～3wt% of binary of fatty acids mono-methyl.
The preparation method of a kind of polyester composite filament arranged side by side the most according to claim 3, it is characterised in that PBT in composite filament
It is 4:6～6:4 with the ratio of PET weight.
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| CN107938002A (en) * | 2017-12-14 | 2018-04-20 | 江苏恒力化纤股份有限公司 | A kind of foreign components composite filament and preparation method thereof |
| CN109024002A (en) * | 2018-07-04 | 2018-12-18 | 杭州奔马化纤纺丝有限公司 | A kind of compound colorful staple fiber and preparation method thereof arranged side by side |
| CN109722728B (en) * | 2018-12-27 | 2020-07-03 | 江苏恒力化纤股份有限公司 | PBT-containing double-component elastic yarn and preparation method thereof |
| CN114592255A (en) * | 2022-03-09 | 2022-06-07 | 舟山欣欣化纤有限公司 | Preparation method of low-temperature dyeable composite elastic fiber |
| CN114645333A (en) * | 2022-03-10 | 2022-06-21 | 江苏嘉通能源有限公司 | Production method and production equipment of polyester parallel composite yarns shaped like Chinese character' wang |
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| CN1630741A (en) * | 2002-02-12 | 2005-06-22 | 齐默尔股份公司 | A process for the production and for the winding of polyester multi-filament yarns as well as the polyester multi-filament yarns obtainable by said method and a device for the winding of one or more m |
| CN101440538A (en) * | 2008-12-31 | 2009-05-27 | 邹祖林 | Novel dual-color side-by-side composite polyester fiber |
| CN101851812A (en) * | 2009-12-18 | 2010-10-06 | 东丽纤维研究所（中国）有限公司 | Parallel composite elastic fiber and manufacture method thereof |
| CN104141178A (en) * | 2014-07-31 | 2014-11-12 | 江苏盛虹科技股份有限公司 | Elastic PET composite fiber and method for preparing elastic PET composite fiber |
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| JPH09316184A (en) * | 1996-05-29 | 1997-12-09 | Asahi Chem Ind Co Ltd | Production of modified polyester |
| KR100531617B1 (en) * | 2004-03-25 | 2005-11-28 | 주식회사 효성 | Conjugated fiber and manufacturing thereof |
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| CN1630741A (en) * | 2002-02-12 | 2005-06-22 | 齐默尔股份公司 | A process for the production and for the winding of polyester multi-filament yarns as well as the polyester multi-filament yarns obtainable by said method and a device for the winding of one or more m |
| CN101440538A (en) * | 2008-12-31 | 2009-05-27 | 邹祖林 | Novel dual-color side-by-side composite polyester fiber |
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