CN106957515A - A kind of PET/PTT blending and modifyings fiber - Google Patents
A kind of PET/PTT blending and modifyings fiber Download PDFInfo
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- CN106957515A CN106957515A CN201710170846.3A CN201710170846A CN106957515A CN 106957515 A CN106957515 A CN 106957515A CN 201710170846 A CN201710170846 A CN 201710170846A CN 106957515 A CN106957515 A CN 106957515A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/48—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of halogenated hydrocarbons
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/9258—Velocity
- B29C2948/9259—Angular velocity
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/12—Applications used for fibers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/08—Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape
- C08L2205/16—Fibres; Fibrils
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/24—Crystallisation aids
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Abstract
A kind of PET/PTT blending and modifyings fiber of disclosure of the invention, including following parts by weight composition:PBT30 parts, PTT15 parts, 5 parts of compatilizer, 0.5 part of nucleation accelerating agent, 20 parts of the modified Teflon fiber modified Teflon fiber include following weight parts composition:Double 5 parts of (dimethylamino) dimethylsilane 1 part of trifluoro propyl trichlorosilane (bromomethyl) 3 parts of trimethyl silane, 10 parts of the compound ethers of 5 parts of polytetrafluoroethylene (PTFE) 100 parts of N (BETA aminoethyls) GAMA aminopropyl trimethoxysilanes.Still there is preferable bending modulus under cold conditions in the present invention.
Description
Technical field
The present invention relates to fiber, more particularly to a kind of PET/PTT blending and modifyings fiber.
Background technology
PET (poly ethylene terephthalate, polyethylene terephthalate) is nineteen fifty-three by Dupont
Company realizes industrialized linear thermoplastic's polymer earliest, be it is a kind of have higher melting temperature (Tm) and glass transition temperature
(Tg) crystalline high polymer, can keep excellent physical property and mechanical property within the scope of wider temperature, it resistance to
Fatigability, rub resistance are excellent, and resistance to ag(e)ing is excellent, and electrical insulating property is protruded, stable to most of organic solvents and inorganic acid, and
And energy consumption is very low, processability is good, thus is widely used in the fields such as synthetic fibers, film and engineering plastics, but by
Make its crystallization rate slower in PET rigidity, the shortcoming of mould temperature height and molding cycle length makes it in engineering plastics
Application in field is restricted.
PTT be by terephthalic acid (TPA) (the application PTT of PTT should
With PTA) and 1,3- propane diols (PDO) polycondensation form, its molecular structural formula is ((CH2) 3O O=C O=CO)) ptt fiber is comprehensive
The flexibility of nylon, the bulkiness of acrylic fibers, the pollution resistance of terylene, add elasticity inherently, and can normal temperature dyeing etc.
Feature, rolls into one the excellent wearability of various fibers, so that as the currently popular macromolecule of recent development in the world
One of new material.
In the prior art, by obtaining elastic preferably fiber for PET and PTT blendings.But in the prior art
PET and PTT blended fibers under cryogenic, elastic modelling quantity can significantly decline.
The content of the invention
In view of the shortcomings of the prior art, it is an object of the invention to provide still have preferably elasticity under a kind of low temperature
The PET/PTT blending and modifying fibers of modulus.
To achieve the above object, the invention provides following technical scheme:
A kind of PET/PTT blending and modifyings fiber, including following parts by weight composition:
30 parts of PBT
15 parts of PTT
5 parts of compatilizer
0.5 part of nucleation accelerating agent
20 parts of modified Teflon fiber
The modified Teflon fiber is constituted including following weight parts:
100 parts of polytetrafluoroethylene (PTFE)
5 parts of N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes
Double 5 parts of (dimethylamino) dimethylsilanes
1 part of trifluoro propyl trichlorosilane
3 parts of (bromomethyl) trimethyl silane
10 parts of compound ether
The preparation method of the modified Teflon is:
By compound ether and N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes, double (dimethylamino) dimethylsilanes,
Double (dimethylamino) dimethylsilanes, (bromomethyl) trimethyl silane enter mixing, are mixed afterwards with polytetrafluoroethylgranule granule,
Modified Teflon is obtained in double screw extruder, modified Teflon fiber is spun to afterwards.
As a further improvement on the present invention,
The compound ether is constituted including following weight parts:
3 parts of 4,4- dinitro diphenyl ethers
4- bromophenyls -3 parts of phenyl ether.
As a further improvement on the present invention,
The compatilizer is the mixing of tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester
Thing.
As a further improvement on the present invention, tetrahydrophthalic acid 2-glycidyl ester and hexahydro are adjacent in the compatilizer
The mass ratio of phthalic acid 2-glycidyl ester is 1:1.
As a further improvement on the present invention, the nucleation accelerating agent is talcum powder.
As a further improvement on the present invention,
Step 1: the mass fraction as described in claim 1 to 5 weighs each component, and by the PET weighed and PBT 110~
Drying time more than 4 hours at a temperature of 130 DEG C, other components are dried more than 2 hours at a temperature of 60~80 DEG C;
Mixed Step 2: the PET after drying process, PTT, compatilizer, nucleation accelerating agent are put into high-speed mixer, in normal temperature
5~15min of lower stirring;
Step 3: the mixed material of step 2 is added in the hopper of double screw extruder, modified Teflon is fine
Tie up and add mouth from the glass in twin-screw stage casing and add, extruded through melt blending, water-cooled, air-dry, pelletizing;
Wherein, the temperature setting of double screw extruder is:One area:200℃;2nd area:220℃;3rd area:220~220 DEG C;4th area:
240℃;5th area:250℃;6th area:250℃;7th area:250℃;8th area:260℃;Head temperature:250℃;Screw speed is controlled
In 200~400r/min.
In the present invention, it is PET and PTT blending first, in Blending Processes, passes through compatilizer and nucleation accelerating agent
Addition enables to the PET and PTT mixing can be fully compatible and nucleation.As the key of the present invention, for polytetrafluoroethylene (PTFE)
It is modified, is by N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes, double (two first in modifying process
Methyl ammonia) dimethylsilane, trifluoro propyl trichlorosilane, the addition of (bromomethyl) trimethyl silane, can be for polytetrafluoroethyl-ne
Alkene is modified so that the material that modified Teflon is prepared into PET and PTT blendings carries out compound tense, can be had more preferable
Combined strength bination, while by the addition of compound ether, overall composite effect can be further improved, while collaboration can be played
Effect so that fiber still has preferably elasticity at low temperature.
Embodiment
Embodiment
A kind of PET/PTT blending and modifyings fiber, including following parts by weight composition:
30 parts of PBT
15 parts of PTT
5 parts of compatilizer
0.5 part of nucleation accelerating agent
20 parts of modified Teflon fiber
The modified Teflon fiber is constituted including following weight parts:
100 parts of polytetrafluoroethylene (PTFE)
5 parts of N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes
Double 5 parts of (dimethylamino) dimethylsilanes
1 part of trifluoro propyl trichlorosilane
3 parts of (bromomethyl) trimethyl silane
10 parts of compound ether
The preparation method of the modified Teflon is:
By compound ether and N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes, double (dimethylamino) dimethylsilanes,
Double (dimethylamino) dimethylsilanes, (bromomethyl) trimethyl silane enter mixing, are mixed afterwards with polytetrafluoroethylgranule granule,
Modified Teflon is obtained in double screw extruder, modified Teflon fiber is spun to afterwards.
The compound ether is constituted including following weight parts:
3 parts of 4,4- dinitro diphenyl ethers
4- bromophenyls -3 parts of phenyl ether.
The compatilizer is tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester
Mixture.
Tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester in the compatilizer
Mass ratio is 1:1.
The nucleation accelerating agent is talcum powder.
Step 1: the mass fraction as described in claim 1 to 5 weighs each component, and by the PET weighed and PBT 110
Drying time more than 4 hours at a temperature of~130 DEG C, other components are dried more than 2 hours at a temperature of 60~80 DEG C;
Mixed Step 2: the PET after drying process, PTT, compatilizer, nucleation accelerating agent are put into high-speed mixer, in normal temperature
5~15min of lower stirring;
Step 3: the mixed material of step 2 is added in the hopper of double screw extruder, modified Teflon is fine
Tie up and add mouth from the glass in twin-screw stage casing and add, extruded through melt blending, water-cooled, air-dry, pelletizing;
Wherein, the temperature setting of double screw extruder is:One area:200℃;2nd area:220℃;3rd area:220~220 DEG C;4th area:
240℃;5th area:250℃;6th area:250℃;7th area:250℃;8th area:260℃;Head temperature:250℃;Screw speed is controlled
In 200~400r/min.
Comparative example one
A kind of PET/PTT blending and modifyings fiber, including following parts by weight composition:
30 parts of PBT
15 parts of PTT
5 parts of compatilizer
0.5 part of nucleation accelerating agent
20 parts of polytetrafluoroethylene fibre
The compatilizer is the mixing of tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester
Thing.
Tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester in the compatilizer
Mass ratio is 1:1.
The nucleation accelerating agent is talcum powder.
Step 1: the mass fraction as described in claim 1 to 5 weighs each component, and by the PET weighed and PBT 110
Drying time more than 4 hours at a temperature of~130 DEG C, other components are dried more than 2 hours at a temperature of 60~80 DEG C;
Mixed Step 2: the PET after drying process, PTT, compatilizer, nucleation accelerating agent are put into high-speed mixer, in normal temperature
5~15min of lower stirring;
Step 3: the mixed material of step 2 is added in the hopper of double screw extruder, by polytetrafluoroethylene fibre from
The glass in twin-screw stage casing adds mouth and added, extruded through melt blending, water-cooled, air-dry, pelletizing;
Wherein, the temperature setting of double screw extruder is:One area:200℃;2nd area:220℃;3rd area:220~220 DEG C;4th area:
240℃;5th area:250℃;6th area:250℃;7th area:250℃;8th area:260℃;Head temperature:250℃;Screw speed is controlled
In 200~400r/min.
Comparative example two
A kind of PET/PTT blending and modifyings fiber, including following parts by weight composition:
30 parts of PBT
15 parts of PTT
5 parts of compatilizer
0.5 part of nucleation accelerating agent
20 parts of modified Teflon fiber
The modified Teflon fiber is constituted including following weight parts:
100 parts of polytetrafluoroethylene (PTFE)
5 parts of N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes
10 parts of 4,4- dinitro diphenyl ethers
The preparation method of the modified Teflon is:
Compound ether is entered to mix with N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes, afterwards and polytetrafluoroethylene (PTFE)
Particle is mixed, and modified Teflon is obtained in double screw extruder, and modified Teflon fiber is spun to afterwards.
The compatilizer is tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester
Mixture.
Tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester in the compatilizer
Mass ratio is 1:1.
The nucleation accelerating agent is talcum powder.
Step 1: the mass fraction as described in claim 1 to 5 weighs each component, and by the PET weighed and PBT 110
Drying time more than 4 hours at a temperature of~130 DEG C, other components are dried more than 2 hours at a temperature of 60~80 DEG C;
Mixed Step 2: the PET after drying process, PTT, compatilizer, nucleation accelerating agent are put into high-speed mixer, in normal temperature
5~15min of lower stirring;
Step 3: the mixed material of step 2 is added in the hopper of double screw extruder, modified Teflon is fine
Tie up and add mouth from the glass in twin-screw stage casing and add, extruded through melt blending, water-cooled, air-dry, pelletizing;
Wherein, the temperature setting of double screw extruder is:One area:200℃;2nd area:220℃;3rd area:220~220 DEG C;4th area:
240℃;5th area:250℃;6th area:250℃;7th area:250℃;8th area:260℃;Head temperature:250℃;Screw speed is controlled
In 200~400r/min.
Comparative example three
A kind of PET/PTT blending and modifyings fiber, including following parts by weight composition:
30 parts of PBT
15 parts of PTT
5 parts of compatilizer
0.5 part of nucleation accelerating agent
20 parts of modified Teflon fiber
The modified Teflon fiber is constituted including following weight parts:
100 parts of polytetrafluoroethylene (PTFE)
1 part of trifluoro propyl trichlorosilane
3 parts of (bromomethyl) trimethyl silane
4- bromophenyls -10 parts of phenyl ether
The preparation method of the modified Teflon is:
Compound ether is entered to mix with double (dimethylamino) dimethylsilanes, (bromomethyl) trimethyl silane, afterwards and polytetrafluoroethyl-ne
Alkene particle is mixed, and modified Teflon is obtained in double screw extruder, modified Teflon is spun to afterwards fine
Dimension.
The compatilizer is tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester
Mixture.
Tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester in the compatilizer
Mass ratio is 1:1.
The nucleation accelerating agent is talcum powder.
Step 1: the mass fraction as described in claim 1 to 5 weighs each component, and by the PET weighed and PBT 110
Drying time more than 4 hours at a temperature of~130 DEG C, other components are dried more than 2 hours at a temperature of 60~80 DEG C;
Mixed Step 2: the PET after drying process, PTT, compatilizer, nucleation accelerating agent are put into high-speed mixer, in normal temperature
5~15min of lower stirring;
Step 3: the mixed material of step 2 is added in the hopper of double screw extruder, modified Teflon is fine
Tie up and add mouth from the glass in twin-screw stage casing and add, extruded through melt blending, water-cooled, air-dry, pelletizing;
Wherein, the temperature setting of double screw extruder is:One area:200℃;2nd area:220℃;3rd area:220~220 DEG C;4th area:
240℃;5th area:250℃;6th area:250℃;7th area:250℃;8th area:260℃;Head temperature:250℃;Screw speed is controlled
In 200~400r/min.
In the present invention, it is PET and PTT blending first, in Blending Processes, passes through compatilizer and nucleation accelerating agent
Addition enables to the PET and PTT mixing can be fully compatible and nucleation.As the key of the present invention, for polytetrafluoroethylene (PTFE)
It is modified, is by N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes, double (two first in modifying process
Methyl ammonia) dimethylsilane, trifluoro propyl trichlorosilane, the addition of (bromomethyl) trimethyl silane, can be for polytetrafluoroethyl-ne
Alkene is modified so that the material that modified Teflon is prepared into PET and PTT blendings carries out compound tense, can be had more preferable
Combined strength bination, while by the addition of compound ether, overall composite effect can be further improved, while collaboration can be played
Effect so that fiber still has preferably elasticity at low temperature.
The above is only the preferred embodiment of the present invention, and protection scope of the present invention is not limited merely to above-mentioned implementation
Example, all technical schemes belonged under thinking of the present invention belong to protection scope of the present invention.It should be pointed out that for the art
Those of ordinary skill for, some improvements and modifications without departing from the principles of the present invention, these improvements and modifications
It should be regarded as protection scope of the present invention.
Claims (6)
1. a kind of PET/PTT blending and modifyings fiber, it is characterised in that:Including following parts by weight composition:
30 parts of PBT
15 parts of PTT
5 parts of compatilizer
0.5 part of nucleation accelerating agent
20 parts of modified Teflon fiber
The modified Teflon fiber is constituted including following weight parts:
100 parts of polytetrafluoroethylene (PTFE)
5 parts of N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes
Double 5 parts of (dimethylamino) dimethylsilanes
1 part of trifluoro propyl trichlorosilane
3 parts of (bromomethyl) trimethyl silane
10 parts of compound ether
The preparation method of the modified Teflon is:
By compound ether and N- (BETA- aminoethyls)-GAMA- aminopropyl trimethoxysilanes, double (dimethylamino) dimethylsilanes,
Double (dimethylamino) dimethylsilanes, (bromomethyl) trimethyl silane enter mixing, are mixed afterwards with polytetrafluoroethylgranule granule,
Modified Teflon is obtained in double screw extruder, modified Teflon fiber is spun to afterwards.
2. a kind of PET/PTT blending and modifyings fiber according to claim 1, it is characterised in that:
The compound ether is constituted including following weight parts:
3 parts of 4,4- dinitro diphenyl ethers
4- bromophenyls -3 parts of phenyl ether.
3. a kind of PET/PTT blending and modifyings fiber according to claim 2, it is characterised in that:
The compatilizer is the mixing of tetrahydrophthalic acid 2-glycidyl ester and hexahydrophthalic acid 2-glycidyl ester
Thing.
4. a kind of PET/PTT blending and modifyings fiber according to claim 3, it is characterised in that:Tetrahydrochysene in the compatilizer
The mass ratio of o-phthalic acid diglycidyl ester and hexahydrophthalic acid 2-glycidyl ester is 1:1.
5. a kind of PET/PTT blending and modifyings fiber according to claim 4, it is characterised in that:The nucleation accelerating agent is
Talcum powder.
6. a kind of preparation method of PET/PTT blending and modifyings fiber, it is characterised in that:
Step 1: the mass fraction as described in claim 1 to 5 weighs each component, and by the PET weighed and PBT 110~
Drying time more than 4 hours at a temperature of 130 DEG C, other components are dried more than 2 hours at a temperature of 60~80 DEG C;
Mixed Step 2: the PET after drying process, PTT, compatilizer, nucleation accelerating agent are put into high-speed mixer, in normal temperature
5~15min of lower stirring;
Step 3: the mixed material of step 2 is added in the hopper of double screw extruder, modified Teflon is fine
Tie up and add mouth from the glass in twin-screw stage casing and add, extruded through melt blending, water-cooled, air-dry, pelletizing;
Wherein, the temperature setting of double screw extruder is:One area:200℃;2nd area:220℃;3rd area:220~220 DEG C;4th area:
240℃;5th area:250℃;6th area:250℃;7th area:250℃;8th area:260℃;Head temperature:250℃;Screw speed is controlled
In 200~400r/min.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113417029A (en) * | 2021-06-24 | 2021-09-21 | 杭州惠丰化纤有限公司 | Elastic sea island yarn and production process thereof |
WO2022148357A1 (en) * | 2021-01-06 | 2022-07-14 | 杜邦中国集团有限公司 | Chemical fibre material made of mixed polyester |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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