CN107988647A - The preparation method of Polyester Porous silk - Google Patents
The preparation method of Polyester Porous silk Download PDFInfo
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- CN107988647A CN107988647A CN201711340299.5A CN201711340299A CN107988647A CN 107988647 A CN107988647 A CN 107988647A CN 201711340299 A CN201711340299 A CN 201711340299A CN 107988647 A CN107988647 A CN 107988647A
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
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- 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
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/24—Formation of filaments, threads, or the like with a hollow structure; Spinnerette packs therefor
- D01D5/247—Discontinuous hollow structure or microporous structure
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- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
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- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/11—Compounds containing epoxy groups or precursors thereof
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- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
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- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/248—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing sulfur
- D06M13/256—Sulfonated compounds esters thereof, e.g. sultones
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- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/292—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
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- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/53—Polyethers
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- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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Abstract
The present invention relates to a kind of preparation method of Polyester Porous silk, polyester fondant is extruded through metering, porous spinneret, cools down, oil, stretching, Polyester Porous silk is made in thermal finalization and winding, the hole count of wherein porous spinneret is 144~288, contain crown ether in the finish to oil, and the content of crown ether is 67.30~85.58wt%, thermal weight loss is less than 15wt% after finish heats 2h at 200 DEG C, and for finish at (50 ± 0.01) DEG C, kinematic viscosity is 27.5~30.1mm2/ s, it is 0.93~0.95mm that finish, which is configured to the kinematic viscosity after the lotion that concentration is 10wt% with water,2/ s, the film strength of finish is 121~127N.Preparation method advantages of simple of the present invention, product, which is made, has soft fine and smooth and good appearance tactile impression advantage.
Description
Technical field
The invention belongs to fiber preparation field, is related to a kind of preparation method of Polyester Porous silk.
Background technology
Polyethylene terephthalate (PET) fiber since the advent of the world, obtains fast because of the excellent performance that it has
Suddenly develop, its yield has become the hat of world's synthetic fibers.Polyester fiber has high fracture strength, elasticity modulus height, returns
Moderate, the thermal finalization excellent performance of elasticity, heat-resisting light resistance be good and a series of excellent performance such as acid-fast alkali-proof good corrosion resistance,
And fabric prepared therefrom has the advantages that crease-resistant and stiffness is good, so, polyester fiber is standby to be widely used in clothes and family
The fields such as spinning.
, must in spinning process since the dielectric constant of most of PET fiber is smaller, regain is relatively low and friction coefficient is higher
Spinning oil must be used.The main component of finish is surfactant, can form oriented attachment layer on chemical fibre surface, i.e., oily
Film, on the one hand, the hydrophilic radical of oil film can adsorb the moisture in air, form continuous water on the fiber surface towards space
Film, makes charged ion that migration occur on it, reduces between fiber because of the accumulation of electrostatic charge caused by friction, so as to reduce
The sheet resistance of fiber, adds the electric conductivity of fiber, and on the other hand, oil film isolation fiber again can produce fiber certain
Affinity, makes it be not at random there are certain convergence, and in addition, oil film also imparts certain smooth of fiber
Property, makes fiber not be damaged in friction process, and has good feel, can be passed through in spinning winding, stretching,
The operational sequence such as dry, eliminates the electrostatic interaction during textile process, will not occur bad around apron, roller, cylinder etc.
Phenomenon, reduces the generation of lousiness and broken end, ensures the quality of fiber product.
After being ruptured due to the oil film of fiber surface under high temperature, high speed and certain pressure, the friction behavior of fiber can be changed,
Cause frictional force to increase, cause fiber the other problems such as lousiness, broken end occur, film strength is higher, is more not easily broken, more favourable
In the spinnability of fiber, when finish equably adsorbs on the fiber surface, surface forms the oil film of distribution uniform, and oil film exists
Fiber is rapid after being stretched and uniformly extends, if the viscosity of finish is excessive, is unfavorable for the scattered of finish, forms uniform oil
Film.And with the development of the high speed of polyester filament, ultrahigh speed and Mobyneb fiber, develop that a kind of heat resistance is good, viscosity
The great realistic meaning of finish low, that film strength is high, Lubricity is good and antistatic property is strong.
In the prior art due to spinneret hole count increase make it is obtained pulp freeness is small subtracts, under the permeability of finish
Drop, so as to influence the quality of fiber.
Therefore, a kind of preparation method of soft fine and smooth and good appearance tactile impression Polyester Porous silk is studied as currently urgently solving
Certainly the problem of.
The content of the invention
The purpose of the invention is to overcome to cause the permeability of finish since pulp freeness is small in the prior art
It is deteriorated, the problem of the friction coefficient increase between silk, the quality decline of silk, there is provided one kind has the soft fine and smooth and appearance tactile impression good
Polyester Porous silk preparation method.The use of the finish of the invention containing crown ether, improves the heat resistance and lubricity of finish, lifting
The quality of fiber.
In order to achieve the above object, the technical solution adopted by the present invention is:
The preparation method of Polyester Porous silk, polyester fondant is extruded through metering, porous spinneret, cools down, oil, stretching,
Polyester Porous silk is made in thermal finalization and winding;
The hole count of the porous spinneret is 144~288;
Contain crown ether in the finish to oil, and the content of crown ether is 67.30~85.58wt%, finish of the present invention
The content of middle crown ether need to be kept within the specific limits, and the addition of crown ether is too low, can not be made that viscosity is low, heat resistance is good and
The higher finish of film strength, the addition of crown ether is excessive, other performance indicators of finish can be affected.
Crown ether is a kind of heterocyclic organic compounds, includes multiple ether groups.The wettability of crown ether-like surfactant
Bigger than corresponding open chain compound, crown ether has preferable solubilising, and salt compounds are relatively low in the solubility of organic compound, but with
The solubility for the organic matter of the addition salt compounds of crown ether is improved.Conventional polyester class compound or polyethers in finish
Class, since molecular weight is larger and the effect of hydrogen bond, intermolecular effect is larger, and it is larger to show as kinematic viscosity, after adding crown ether,
Crown ether can be preferably compatible in polyesters compound or polyethers finish system, into polyesters compound or polyethers quasi-molecule
Between chain, the active force between strand is shielded, so as to cause the viscosity of finish system to reduce.Preparation medium is antistatic at the same time
Agent is broadly divided into anionic, cationic and amphoteric surfactant, is mostly deposited containing metal ion or in a salt form
This all makes antistatic additive and polyesters compound in finish or the phase tolerance of polyethers, the addition of crown ether, due to the molten effect of salt
Should, antistatic additive and polyesters compound or the compatibility of polyethers are improved, and then finish oil film strength is improved, this is right
The stability and the product amount of holding of spinning have larger meaning.The index of finish is the embodiment of a composite factor, thus to crown ether
Addition propose certain restriction, too low heat resistance, the advantage of film strength to finish embodies inadequate, and excessive other refer to
Rotating savings is restricted.
As preferable technical solution:
The preparation method of Polyester Porous silk as described above, thermal weight loss is less than after the finish heats 2h at 200 DEG C
15wt%, crown ether have the volatilization point of higher and excellent heat-resistant stability, and the heat resistance of the finish introduced after crown ether also obtains
To being obviously improved;
For the finish at (50 ± 0.01) DEG C, kinematic viscosity is 27.5~30.1mm2/ s, the finish are configured to water
Kinematic viscosity after the lotion that concentration is 10wt% is 0.93~0.95mm2/ s, the viscosity that crown ether can reduce finish are mainly
Since crown ether oneself viscosity is relatively low and is pearl small molecule, after introducing crown ether in finish system, crown ether can be preferably compatible to
In polyesters compound or polyether compound finish system, while enter polyesters compound or polyether compound strand
Between, the active force between strand is shielded, so as to reduce the viscosity of finish system;
The film strength of the finish is 121~127N, and the film strength of finish is relatively low in the prior art, generally in 110N
Left and right, this mostly exists containing metal ion or in a salt form mainly due to the antistatic additive of preparation medium, causes to resist
Electrostatic agent can improve film strength and be mainly with polyesters compound or the poor compatibility of polyether compound in finish, crown ether
Salting in effect can be produced after being added due to crown ether, improves antistatic additive and polyesters compound or the compatibility of polyethers,
And then improve finish oil film strength;
The surface tension of the finish is 23.2~26.8cN/cm, and ratio resistance is 1.0 × 108~1.8 × 108Ω·cm;
After oiling, confficient of static friction between fiber and fiber is 0.250~0.263, the coefficient of kinetic friction for 0.262~
0.273;
After oiling, confficient of static friction between fiber and metal is 0.202~0.210, the coefficient of kinetic friction for 0.320~
0.332。
The preparation method of Polyester Porous silk as described above, the finish when in use, with water be configured to concentration for 10~
The emulsion of 20wt%.
The preparation method of Polyester Porous silk as described above, the crown ether is 2- methylols -12-crown-4,15- crown ethers -5 or
2- methylol -15- crown-s 5.
The preparation method of Polyester Porous silk as described above, also containing mineral oil, phosphate kalium salt, three hydroxyls in the finish
Methylpropane laurate and sodium alkyl sulfonate.
The preparation method of Polyester Porous silk as described above, the mineral oil are one kind in the mineral oil of 9#~17#;
The phosphate kalium salt is 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, isomerous tridecanol polyoxyethylene ether phosphate kalium salt or ten
Tetracosanol phosphate kalium salt;
The sodium alkyl sulfonate is dodecyl sodium sulfate, pentadecyl sulfonic acid sodium or sodium cetanesulfonate.
The preparation method of Polyester Porous silk as described above, the preparation method of the finish are:By crown ether and phosphate potassium
Salt, trimethylolpropane laurate and sodium alkyl sulfonate are added in mineral oil are uniformly mixing to obtain finish after mixing;
Count in parts by weight, the addition of each component is as follows:
The mixing carries out at normal temperatures, and the temperature of the stirring is 40~55 DEG C, and the time is 1~3h.
The preparation method of Polyester Porous silk as described above, the spinning technology parameter of the Polyester Porous silk are as follows:
Spinning temperature:280~290 DEG C;
Cooling temperature:20~25 DEG C;
Network pressure:0.20~0.30MPa;
One roller speed:2200~2600m/min
One roll temperature:75~85 DEG C;
Two roller speeds:3600~3900m/min;
Two roll temperatures:135~165 DEG C;
The speed of winding:3550~3840m/min;
The initial pressure of filament spinning component is 120bar, and pressure rises Δ P≤0.6bar/ days.
The preparation method of Polyester Porous silk as described above, the fiber number of the Polyester Porous silk is 75~150dtex, fracture
Intensity >=3.8cN/dtex, elongation at break are 33.0 ± 3.0%, line density deviation ratio≤0.5%, fracture strength CV values≤
5.0%, extension at break CV value≤8.0%, yarn unevenness CV value≤2.00%, boiling water shrinkage is 7.5 ± 0.5%, oil-containing
Rate is 0.90 ± 0.20%, more than 4.5 grades of dyeing uniformity.
The preparation method of Polyester Porous silk as described above, the dyeing of the Polyester Porous silk are:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h;
Wherein, dyeing is Disperse Red 3B, disperse blue SE-2R with disperse dyes or disperses bright blue S-GL, and dye dosage is
2.0% (o.w.f), the concentration of dispersant NNO is 1.2g/L in dye liquor, and the pH value of dye liquor is 5, bath raio 1:50.
Invention mechanism:
The present invention has been made that a kind of viscosity is low, heat resistance is good and film strength is higher by introducing crown ether in finish
Finish.The viscosity of finish is higher mainly due to containing conventional polyester class compound or polyethers chemical combination in finish in the prior art
Thing, for such compound since molecular weight is larger and the effect of hydrogen bond, its intermolecular larger kinematic viscosity that shows as of effect is larger,
Thus cause the viscosity of finish higher, the viscosity of finish can significantly reduce after addition crown ether, viscous mainly due to crown ether itself
To spend relatively low and be pearl small molecule, crown ether can be preferably compatible in polyesters compound or polyethers finish system, while into
Enter between polyesters compound or polyether compound strand, the active force between strand is shielded, so as to reduce finish body
The viscosity of system.The relatively low antistatic additive mainly due to preparation medium of the film strength of finish mostly contains metal in the prior art
Ion exists in a salt form, causes antistatic additive and the poor compatibility of polyesters compound or polyethers in finish, hat
Ether, which can be improved after film strength is added mainly due to crown ether, can produce salting in effect, improve antistatic additive and polyesters
The compatibility of compound or polyethers, and then improve finish oil film strength.In addition, crown ether has the volatilization point of higher and excellent
Good heat-resistant stability, the heat resistance of the finish introduced after crown ether are also obviously improved.
The finish viscosity that the present invention uses is low, and permeability is high, and lubricity is good, precursor can be made to pass through spinning.Can be with
The film of the high protectiveness of one layer of intensity is formed on fiber precursor surface, prevents fibre damage of the precursor in spinning process.
It will not cause filametntary fracture in spinning process because of the generation of electrostatic problem, influence product quality, so that final system
The excellent properties that the composite filament obtained has soft fine and smooth, elasticity well and quality is high.
Beneficial effect:
(1) a kind of preparation method of Polyester Porous silk of the invention, preparation flow advantages of simple, obtained drafting silk have
The advantages of soft exquisiteness and good appearance tactile impression;
(2) preparation method of a kind of Polyester Porous silk of the invention, using porous spinneret, obtained fiber is thinner, soft
It is soft more preferable;
(3) a kind of preparation method of Polyester Porous silk of the invention, preparation process advantages of simple, make finish permeability high,
Obtained fiber lousiness is few;
(4) preparation method of a kind of Polyester Porous silk of the invention, the oil agent containing crown ether used during oiling
Have the characteristics that viscosity is low, heat resistance is good, film strength is high, Lubricity is good and antistatic property is strong, improve spinning
The processing performance of stability and fiber.
Embodiment
The invention will be further elucidated with reference to specific embodiments.It is to be understood that these embodiments are merely to illustrate this hair
It is bright rather than limit the scope of the invention.In addition, it should also be understood that, after reading the content taught by the present invention, art technology
Personnel can make various changes or modifications the present invention, and such equivalent forms equally fall within the application the appended claims and limited
Fixed scope.
Embodiment 1
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylols -12-crown-4 and 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, trimethylolpropane
Laurate and dodecyl sodium sulfate are added in 9# mineral oil and in 40 DEG C of uniform stirring 1h after mixing at normal temperatures
Obtain finish;Count in parts by weight, the addition of each component is as follows:2 parts of 9# mineral oil;Trimethylolpropane laurate 10
Part;2- methylols -90 parts of 12-crown-4;8 parts of 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite;3 parts of dodecyl sodium sulfate.The finish prepared
The content of middle crown ether is 79.6wt%, and the resistance to elevated temperatures of finish is excellent, and thermal weight loss is after heating 2h at 200 DEG C
14.5wt%;The viscosity of finish is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 29.6mm2/ s, being configured to concentration with water is
Kinematic viscosity after the lotion of 10wt% is 0.93mm2/s;The film strength of finish is higher, film strength 125N, finish
Surface tension is 24.8cN/cm, and ratio resistance is 1.3 × 108Ω cm, after oiling, the static friction between fiber and fiber (F/F)
Coefficient (μs) it is 0.255, the coefficient of kinetic friction (μd) it is 0.266, the confficient of static friction (μ between fiber and metal (F/M)s) be
0.203, the coefficient of kinetic friction (μd) it is 0.320, the finish of preparation is configured to the emulsification that concentration is 15wt% when in use, with water
Liquid;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 158.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 80dtex, fracture strength 3.9cN/dtex, and elongation at break is
30.0%, line density deviation ratio is 0.42%, and fracture strength CV values are 4.9%, and extension at break CV values are 7.7%, evenness fault
Rate CV values are 1.98%, boiling water shrinkage 7.0%, oil content 1.10%, 4.5 grades of dyeing uniformity.
Embodiment 2
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 15- crown ethers -5 and isomerous tridecanol polyoxyethylene ether phosphate kalium salt, three hydroxyl first
Base propane laurate and pentadecyl sulfonic acid sodium be added to after mixing at normal temperatures in 10# mineral oil and 43 DEG C uniformly
Stirring 1.5h obtains finish;Count in parts by weight, the addition of each component is as follows:2 parts of 10# mineral oil;The trimethylolpropane moon
15 parts of cinnamic acid ester;- 5 70 parts of 15- crown ethers;10 parts of isomerous tridecanol polyoxyethylene ether phosphate kalium salt;Pentadecyl sulfonic acid sodium 7
Part.The content of crown ether is 67.30wt% in the finish prepared, and the resistance to elevated temperatures of finish is excellent, heats 2h at 200 DEG C
Thermal weight loss is 13wt% afterwards, and the viscosity of finish is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 28.1mm2/ s, is configured with water
The kinematic viscosity after lotion for being 10wt% into concentration is 0.93mm2/ s, the film strength of finish is higher, is 123N, finish
Surface tension is 25.1cN/cm, and ratio resistance is 1.5 × 108Ω cm, after oiling, the static friction between fiber and fiber (F/F)
Coefficient (μs) it is 0.257, the coefficient of kinetic friction (μd) it is 0.265, after oiling, the confficient of static friction between fiber and metal (F/M)
(μs) it is 0.205, the coefficient of kinetic friction (μd) it is 0.323, when in use, it is 14wt%'s to be configured to concentration with water to the finish of preparation
Emulsion;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 176.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 100dtex, fracture strength 4.2cN/dtex, and elongation at break is
30.0%, line density deviation ratio is 0.49%, and fracture strength CV values are 4.5%, and extension at break CV values are 7.6%, evenness fault
Rate CV values are 1.94%, boiling water shrinkage 7.0%, oil content 0.90%, 4.5 grades of dyeing uniformity.
Embodiment 3
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylol -15- crown-s 5 and ten tetracosanol phosphate kalium salts, trihydroxy methyl third
Alkane laurate and pentadecyl sulfonic acid sodium are added in 11# mineral oil and in 48 DEG C of uniform stirrings after mixing at normal temperatures
3h obtains finish;Count in parts by weight, the addition of each component is as follows:8 parts of 11# mineral oil;Trimethylolpropane laurate
10 parts;
585 parts of 2- methylol -15- crown-s;Ten 11 parts of tetracosanol phosphate kalium salts;5 parts of pentadecyl sulfonic acid sodium.Prepare
The content of crown ether is 70.83wt% in the finish gone out, and the resistance to elevated temperatures of finish is excellent, and heat is lost after heating 2h at 200 DEG C
Weight is 11wt%, and the viscosity of finish is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 30.1mm2/ s, concentration is configured to water
It is 0.94mm for the kinematic viscosity after the lotion of 10wt%2/ s, the film strength of finish is higher, is 125N.The surface of finish
Power is 23.2cN/cm, and ratio resistance is 1.8 × 108Ω cm, after oiling, the confficient of static friction between fiber and fiber (F/F)
(μs) it is 0.250, the coefficient of kinetic friction (μd) it is 0.272, after oiling, the confficient of static friction (μ between fiber and metal (F/M)s) be
0.209, the coefficient of kinetic friction (μd) it is 0.329, the finish of preparation is configured to the emulsification that concentration is 10wt% when in use, with water
Liquid;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 144.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 135dtex, fracture strength 4.0cN/dtex, and elongation at break is
33.0%, line density deviation ratio is 0.48%, and fracture strength CV values are 5.0%, and extension at break CV values are 7.3%, evenness fault
Rate CV values are 1.96%, boiling water shrinkage 7.5%, oil content 0.90%, 5.0 grades of dyeing uniformity.
Embodiment 4
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylols -12-crown-4 and 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, trimethylolpropane
Laurate and sodium cetanesulfonate are added in 12# mineral oil and in 40 DEG C of uniform stirrings after mixing at normal temperatures
2.5h obtains finish;Count in parts by weight, the addition of each component is as follows:5 parts of 12# mineral oil;2- methylols -12-crown-4 95
Part;9 parts of 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite;2 parts of sodium cetanesulfonate.The content of crown ether is in the finish prepared
85.58wt%, the resistance to elevated temperatures of finish is excellent, and thermal weight loss is 9wt% after heating 2h at 200 DEG C, the viscosity of finish compared with
It is low, at (50 ± 0.01) DEG C, kinematic viscosity 29.5mm2/ s, the movement being configured to water after the lotion that concentration is 10wt%
Viscosity is 0.93mm2/ s, the film strength of finish is higher, is 121N, the surface tension of finish is 24.3cN/cm, and ratio resistance is
1.0×108Ω cm, after oiling, the confficient of static friction (μ between fiber and fiber (F/F)s) it is 0.260, the coefficient of kinetic friction
(μd) it is 0.263, after oiling, the confficient of static friction (μ between fiber and metal (F/M)s) it is 0.202, the coefficient of kinetic friction (μd) be
0.330, the finish of preparation is configured to the emulsion that concentration is 16wt% when in use, with water;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 252.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 150dtex, fracture strength 4.3cN/dtex, and elongation at break is
36.0%, line density deviation ratio is 0.45%, and fracture strength CV values are 4.8%, and extension at break CV values are 7.9%, evenness fault
Rate CV values are 1.90%, boiling water shrinkage 8.0%, oil content 0.70%, 5.5 grades of dyeing uniformity.
Embodiment 5
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 15- crown ethers -5 and isomerous tridecanol polyoxyethylene ether phosphate kalium salt, three hydroxyl first
Base propane laurate and dodecyl sodium sulfate be added to after mixing at normal temperatures in 13# mineral oil and 52 DEG C uniformly
Stirring 2h obtains finish;Count in parts by weight, the addition of each component is as follows:10 parts of 13# mineral oil;Trimethylolpropane bay
5 parts of acid esters;- 5 70 parts of 15- crown ethers;8 parts of isomerous tridecanol polyoxyethylene ether phosphate kalium salt;6 parts of dodecyl sodium sulfate.System
Content for crown ether in the finish gone out is 70.70wt%, and the resistance to elevated temperatures of finish is excellent, the heat after 200 DEG C of heating 2h
Weightlessness is 13.5wt%, and the viscosity of finish is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 28.6mm2/ s, is configured to water
Kinematic viscosity after the lotion that concentration is 10wt% is 0.95mm2/ s, the film strength of finish is higher, is 126N, the table of finish
Face tension force is 24.9cN/cm, and ratio resistance is 1.2 × 108Ω cm, after oiling, the static friction system between fiber and fiber (F/F)
Number (μs) it is 0.251, the coefficient of kinetic friction (μd) it is 0.262, after oiling, the confficient of static friction (μ between fiber and metal (F/M)s)
For 0.202, the coefficient of kinetic friction (μd) it is 0.332, the finish of preparation is configured to the emulsification that concentration is 18wt% when in use, with water
Liquid;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 208.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 145dtex, fracture strength 3.8cN/dtex, and elongation at break is
31.0%, line density deviation ratio is 0.41%, and fracture strength CV values are 4.1%, and extension at break CV values are 7.1%, evenness fault
Rate CV values are 1.96%, boiling water shrinkage 7.4%, oil content 1.00%, 4.5 grades of dyeing uniformity.
Embodiment 6
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylol -15- crown-s 5 and ten tetracosanol phosphate kalium salts, trihydroxy methyl third
Alkane laurate and pentadecyl sulfonic acid sodium are added in 14# mineral oil and in 55 DEG C of uniform stirrings after mixing at normal temperatures
1h obtains finish;Count in parts by weight, the addition of each component is as follows:3 parts of 14# mineral oil;Trimethylolpropane laurate
10 parts;5 75 parts of 2- methylol -15- crown-s;Ten 14 parts of tetracosanol phosphate kalium salts;7 parts of pentadecyl sulfonic acid sodium.Prepare
Finish in the content of crown ether be 68.80wt%, the resistance to elevated temperatures of finish is excellent, heats thermal weight loss after 2h at 200 DEG C
For 12wt%, the viscosity of finish is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 27.5mm2/ s, being configured to concentration with water is
Kinematic viscosity after the lotion of 10wt% is 0.95mm2/ s, the film strength of finish is higher, is 126N.The surface tension of finish
For 25.4cN/cm, ratio resistance is 1.6 × 108Ω cm, after oiling, the confficient of static friction (μ between fiber and fiber (F/F)s)
For 0.255, the coefficient of kinetic friction (μd) it is 0.267, after oiling, the confficient of static friction (μ between fiber and metal (F/M)s) be
0.203, the coefficient of kinetic friction (μd) it is 0.330, the finish of preparation is configured to the emulsification that concentration is 17wt% when in use, with water
Liquid;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 288.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 75dtex, fracture strength 3.9cN/dtex, and elongation at break is
35.0%, line density deviation ratio is 0.49%, and fracture strength CV values are 4.4%, and extension at break CV values are 7.5%, evenness fault
Rate CV values are 1.93%, boiling water shrinkage 7.4%, oil content 0.95%, 4.5 grades of dyeing uniformity.
Embodiment 7
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 15- crown ethers -5 and 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, trimethylolpropane laurate
Ester and sodium cetanesulfonate are added in 15# mineral oil and obtain oil in 41 DEG C of uniform stirring 2h after mixing at normal temperatures
Agent;Count in parts by weight, the addition of each component is as follows:8 parts of 15# mineral oil;20 parts of trimethylolpropane laurate;15-
100 parts of crown ether -5;15 parts of 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite;2 parts of sodium cetanesulfonate.Crown ether contains in the finish prepared
Measure as 68.97wt%, the resistance to elevated temperatures of finish is excellent, and thermal weight loss is 8.5wt% after heating 2h at 200 DEG C, finish
Viscosity is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 28.4mm2/ s, after the lotion that concentration is 10wt% is configured to water
Kinematic viscosity be 0.94mm2/ s, the film strength of finish is higher, is 122N.The surface tension of finish is 26.8cN/cm, than
Resistance is 1.8 × 108Ω cm, after oiling, the confficient of static friction (μ between fiber and fiber (F/F)s) it is 0.263, dynamic friction
Coefficient (μd) it is 0.268, after oiling, the confficient of static friction (μ between fiber and metal (F/M)s) it is 0.210, the coefficient of kinetic friction
(μd) it is 0.320, the finish of preparation is configured to the emulsion that concentration is 20wt% when in use, with water;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 236.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 95dtex, fracture strength 4.4cN/dtex, and elongation at break is
35.5%, line density deviation ratio is 0.5%, and fracture strength CV values are 4.6%, and extension at break CV values are 8.0%, yarn unevenness
CV values are 1.92%, boiling water shrinkage 7.3%, oil content 0.78%, 5.0 grades of dyeing uniformity.
Embodiment 8
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylols -12-crown-4 and ten tetracosanol phosphate kalium salts, trihydroxy methyl third
Alkane laurate and pentadecyl sulfonic acid sodium are added in 16# mineral oil and in 45 DEG C of uniform stirrings after mixing at normal temperatures
3h obtains finish;Count in parts by weight, the addition of each component is as follows:9 parts of 16# mineral oil;2- methylols -12-crown-4 80
Part;Ten 12 parts of tetracosanol phosphate kalium salts;5 parts of pentadecyl sulfonic acid sodium.The content of crown ether is in the finish prepared
83.33wt%, the resistance to elevated temperatures of finish is excellent, and thermal weight loss is 14wt% after heating 2h at 200 DEG C, the viscosity of finish compared with
It is low, at (50 ± 0.01) DEG C, kinematic viscosity 30.0mm2/ s, the movement being configured to water after the lotion that concentration is 10wt%
Viscosity is 0.93mm2/ s, the film strength of finish is higher, is 127N.The surface tension of finish is 23.5cN/cm, and ratio resistance is
1.5×108Ω cm, after oiling, the confficient of static friction (μ between fiber and fiber (F/F)s) it is 0.262, the coefficient of kinetic friction
(μd) it is 0.273, after oiling, the confficient of static friction (μ between fiber and metal (F/M)s) it is 0.208, the coefficient of kinetic friction (μd) be
0.328, the finish of preparation is configured to the emulsion that concentration is 18wt% when in use, with water;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 196.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 90dtex, fracture strength 4.2cN/dtex, and elongation at break is
33.0%, line density deviation ratio is 0.44%, and fracture strength CV values are 4.9%, and extension at break CV values are 7.2%, evenness fault
Rate CV values are 2.00%, boiling water shrinkage 8.0%, oil content 0.90%, 5.5 grades of dyeing uniformity.
Embodiment 9
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylol -15- crown-s 5 and 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, trimethylolpropane
Laurate and dodecyl sodium sulfate after mixing and obtain finish in 55 DEG C of uniform stirring 3h at normal temperatures;By weight
Number meter, the addition of each component are as follows:15 parts of trimethylolpropane laurate;5 90 parts of 2- methylol -15- crown-s;Dodecane
8 parts of base phosphate kalium salt;7 parts of dodecyl sodium sulfate.The content of crown ether is 81.81wt% in the finish prepared, finish
Resistance to elevated temperatures is excellent, and thermal weight loss is 10wt% after heating 2h at 200 DEG C, and the viscosity of finish is relatively low, in (50 ± 0.01)
DEG C when, kinematic viscosity 29.7mm2/ s, the kinematic viscosity being configured to water after the lotion that concentration is 10wt% is 0.94mm2/ s,
The film strength of finish is higher, is 126N.The surface tension of finish is 24.8cN/cm, and ratio resistance is 1.8 × 108Ω cm, on
After oil, the confficient of static friction (μ between fiber and fiber (F/F)s) it is 0.250, the coefficient of kinetic friction (μd) it is 0.264, after oiling,
Confficient of static friction (μ between fiber and metal (F/M)s) it is 0.210, the coefficient of kinetic friction (μd) it is 0.321, the finish of preparation exists
In use, it is configured to the emulsion that concentration is 17wt% with water;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 237.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 115dtex, fracture strength 4.7cN/dtex, and elongation at break is
30.0%, line density deviation ratio is 0.47%, and fracture strength CV values are 4.7%, and extension at break CV values are 7.5%, evenness fault
Rate CV values are 1.96%, boiling water shrinkage 7.5%, oil content 0.90%, 4.5 grades of dyeing uniformity.
Embodiment 10
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylol -15- crown-s 5 and 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, trimethylolpropane
Laurate and dodecyl sodium sulfate after mixing and obtain finish in 55 DEG C of uniform stirring 3h at normal temperatures;By weight
Number meter, the addition of each component are as follows:15 parts of trimethylolpropane laurate;5 90 parts of 2- methylol -15- crown-s;Dodecane
8 parts of base phosphate kalium salt;7 parts of dodecyl sodium sulfate.The content of crown ether is 81.81wt% in the finish prepared, finish
Resistance to elevated temperatures is excellent, and thermal weight loss is 10wt% after heating 2h at 200 DEG C, and the viscosity of finish is relatively low, in (50 ± 0.01)
DEG C when, kinematic viscosity 29.7mm2/ s, the kinematic viscosity being configured to water after the lotion that concentration is 10wt% is 0.94mm2/ s,
The film strength of finish is higher, is 126N, the surface tension of finish is 24.8cN/cm, and ratio resistance is 1.8 × 108Ω cm, on
After oil, the confficient of static friction (μ between fiber and fiber (F/F)s) it is 0.250, the coefficient of kinetic friction (μd) it is 0.264, after oiling,
Confficient of static friction (μ between fiber and metal (F/M)s) it is 0.210, the coefficient of kinetic friction (μd) it is 0.321, the finish of preparation exists
In use, it is configured to the emulsion that concentration is 19wt% with water;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 260.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 140dtex, fracture strength 3.8cN/dtex, and elongation at break is
36.0%, line density deviation ratio is 0.5%, and fracture strength CV values are 4.2%, and extension at break CV values are 7.6%, yarn unevenness
CV values are 1.95%, boiling water shrinkage 7.0%, oil content 1.10%, 4.5 grades of dyeing uniformity.
Embodiment 11
A kind of preparation method of Polyester Porous silk, comprises the following steps that:
(1) oil and prepared with finish:By 2- methylols -12-crown-4 and 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, trimethylolpropane
Laurate and dodecyl sodium sulfate are added in 9# mineral oil and in 40 DEG C of uniform stirring 1h after mixing at normal temperatures
Obtain finish;Count in parts by weight, the addition of each component is as follows:2 parts of 9# mineral oil;Trimethylolpropane laurate 10
Part;2- methylols -90 parts of 12-crown-4;8 parts of 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite;3 parts of dodecyl sodium sulfate.The finish prepared
The content of middle crown ether is 79.6wt%, and the resistance to elevated temperatures of finish is excellent, and thermal weight loss is after heating 2h at 200 DEG C
14.5wt%, the viscosity of finish is relatively low, at (50 ± 0.01) DEG C, kinematic viscosity 29.6mm2/ s, being configured to concentration with water is
Kinematic viscosity after the lotion of 10wt% is 0.93mm2/ s, the film strength of finish is higher, film strength 125N, finish
Surface tension is 24.8cN/cm, and ratio resistance is 1.3 × 108Ω cm, after oiling, the static friction between fiber and fiber (F/F)
Coefficient (μs) it is 0.255, the coefficient of kinetic friction (μd) it is 0.266, after oiling, the confficient of static friction between fiber and metal (F/M)
(μs) it is 0.203, the coefficient of kinetic friction (μd) it is 0.320, when in use, it is 15wt%'s to be configured to concentration with water to the finish of preparation
Emulsion;
(2) polyester fondant extruded through metering, porous spinneret, cooled down, oiled, stretched, thermal finalization and winding are made and wash
Synthetic fibre porous yarn, wherein the hole count of porous spinneret is 144.
The dyeing of Polyester Porous silk is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, 60 DEG C
Enter dye, be warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h, wherein, dyeing with disperse dyes be Disperse Red 3B,
Disperse blue SE-2R disperses bright blue S-GL, and dye dosage is 2.0% (o.w.f), and the concentration of dispersant NNO is 1.2g/ in dye liquor
L, the pH value of dye liquor is 5, bath raio 1:50.
The spinning technology parameter of Polyester Porous silk is shown in Table 1.
The fiber number of obtained Polyester Porous silk is 125dtex, fracture strength 4.1cN/dtex, and elongation at break is
33.0%, line density deviation ratio is 0.43%, and fracture strength CV values are 4.8%, and extension at break CV values are 8.0%, evenness fault
Rate CV values are 1.99%, boiling water shrinkage 7.5%, oil content 0.70%, 4.5 grades of dyeing uniformity.
Table 1
Claims (10)
1. the preparation method of Polyester Porous silk, it is characterized in that:By polyester fondant through metering, porous spinneret extrusion, cooling, on
Polyester Porous silk is made in oil, stretching, thermal finalization and winding;
The hole count of the porous spinneret is 144~288;
Contain crown ether in the finish to oil, and the content of crown ether is 67.30~85.58wt%.
2. the preparation method of Polyester Porous silk according to claim 1, it is characterised in that the finish is in 200 DEG C of heating
Thermal weight loss is less than 15wt% after processing 2h;
For the finish at (50 ± 0.01) DEG C, kinematic viscosity is 27.5~30.1mm2/ s, the finish are configured to concentration with water
It is 0.93~0.95mm for the kinematic viscosity after the lotion of 10wt%2/s;
The film strength of the finish is 121~127N;
The surface tension of the finish is 23.2~26.8cN/cm, and ratio resistance is 1.0 × 108~1.8 × 108Ω·cm;
After oiling, the confficient of static friction between fiber and fiber is 0.250~0.263, and the coefficient of kinetic friction is 0.262~0.273;
After oiling, the confficient of static friction between fiber and metal is 0.202~0.210, and the coefficient of kinetic friction is 0.320~0.332.
3. the preparation method of Polyester Porous silk according to claim 1 or 2, it is characterised in that the finish when in use,
The emulsion that concentration is 10~20wt% is configured to water.
4. the preparation method of Polyester Porous silk according to claim 3, it is characterised in that the crown ether for 2- methylols-
12-crown-4,15- crown ethers -5 or 2- methylol -15- crown-s 5.
5. the preparation method of Polyester Porous silk according to claim 4, it is characterised in that also contain mineral in the finish
Oil, phosphate kalium salt, trimethylolpropane laurate and sodium alkyl sulfonate.
6. the preparation method of Polyester Porous silk according to claim 5, it is characterised in that the mineral oil is 9#~17#
Mineral oil in one kind;
The phosphate kalium salt is 1-isobutyl-3,5-dimethylhexylphosphoric acid sylvite, isomerous tridecanol polyoxyethylene ether phosphate kalium salt or 12
Tetrol phosphate kalium salt;
The sodium alkyl sulfonate is dodecyl sodium sulfate, pentadecyl sulfonic acid sodium or sodium cetanesulfonate.
7. the preparation method of Polyester Porous silk according to claim 6, it is characterised in that the preparation method of the finish
For:Crown ether and phosphate kalium salt, trimethylolpropane laurate and sodium alkyl sulfonate are added to mineral oil after mixing
In be uniformly mixing to obtain finish;Count in parts by weight, the addition of each component is as follows:
The mixing carries out at normal temperatures, and the temperature of the stirring is 40~55 DEG C, and the time is 1~3h.
8. according to claim 1,2 and the preparation method of 4~7 any one of them Polyester Porous silks, it is characterised in that described to wash
The spinning technology parameter of synthetic fibre porous yarn is as follows:
Spinning temperature:280~290 DEG C;
Cooling temperature:20~25 DEG C;
Network pressure:0.20~0.30MPa;
One roller speed:2200~2600m/min
One roll temperature:75~85 DEG C;
Two roller speeds:3600~3900m/min;
Two roll temperatures:135~165 DEG C;
The speed of winding:3550~3840m/min;
The initial pressure of filament spinning component is 120bar, and pressure rises Δ P≤0.6bar/ days.
9. the preparation method of Polyester Porous silk according to claim 8, it is characterised in that the fiber number of the Polyester Porous silk
For 75~150dtex, fracture strength >=3.8cN/dtex, elongation at break is 33.0 ± 3.0%, line density deviation ratio≤
0.5%, fracture strength CV value≤5.0%, extension at break CV value≤8.0%, yarn unevenness CV value≤2.00%, boiling shrinkage
Rate is 7.5 ± 0.5%, and oil content is 0.90 ± 0.20%, more than 4.5 grades of dyeing uniformity.
10. the preparation method of Polyester Porous silk according to claim 9, it is characterised in that the dye of the Polyester Porous silk
Color technique is:
Polyester Porous silk dyes after being handled 30 minutes at 60 DEG C with nonionic surfactant in high temperature and pressure machine, and 60 DEG C enter
Dye, is warming up to 90 DEG C, 100 DEG C, 110 DEG C, 120 DEG C of each constant temperature dyeing 1h;
Wherein, dyeing is Disperse Red 3B, disperse blue SE-2R with disperse dyes or disperses bright blue S-GL, dye dosage 2.0%
(o.w.f), the concentration of dispersant NNO is 1.2g/L in dye liquor, and the pH value of dye liquor is 5, bath raio 1:50.
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CN201711340299.5A CN107988647B (en) | 2017-12-14 | 2017-12-14 | Preparation method of polyester porous yarn |
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