CN105420841A - Pre-orientated polyester filament yarn and manufacturing method thereof - Google Patents

Pre-orientated polyester filament yarn and manufacturing method thereof Download PDF

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Publication number
CN105420841A
CN105420841A CN201610014001.0A CN201610014001A CN105420841A CN 105420841 A CN105420841 A CN 105420841A CN 201610014001 A CN201610014001 A CN 201610014001A CN 105420841 A CN105420841 A CN 105420841A
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China
Prior art keywords
pet polyester
continuous yarn
preparation
terylene pre
tropism continuous
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CN201610014001.0A
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CN105420841B (en
Inventor
周克含
毛佳枫
陈志高
李永军
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ZHEJIANG HENGBAIHUA CHEMICAL FIBER Co Ltd
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ZHEJIANG HENGBAIHUA CHEMICAL FIBER Co Ltd
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/92Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • D01F1/106Radiation shielding agents, e.g. absorbing, reflecting agents

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Woven Fabrics (AREA)
  • Artificial Filaments (AREA)

Abstract

The invention discloses pre-orientated polyester filament yarn and a manufacturing method thereof. The manufacturing method comprises the following steps that 1, a fiber-grade PET board is cut into chips, and the PET chips are dried for twice to enable the moisture content of the PET chips to be smaller than or equal to 25 ppm; dried PET chips are fused, hexadecyl trimethyl silver ammonium bromide, 1,1'-sulfo-bis(2-naphthol), 2-hydroxybenzophenone and a nickelous EDTA complex are added after the dried PET chips are completely fused, and after the materials are evenly mixed, filamentation is performed through extrusion forming and cooling is performed; 2, PET yarn obtained in the step 1 is sequentially processed through collecting through a first roller, heating through an upper heating box, twisting through a heater, drawing through a second roller, sizing through a lower heating box, further sizing through a third roller, oiling through an oiling device and forming through a winding roll to obtain the pre-orientated polyester filament yarn, wherein a chemical fiber oiling agent is contained in the oiling device, and the production speed of the pre-orientated polyester filament yarn is controlled at 3300 rad/min. The pre-orientated polyester filament yarn has the better anti-ultraviolet property and the higher breaking strength.

Description

Terylene pre-tropism continuous yarn and manufacture method thereof
Technical field
The present invention relates to synthetic fiber technical field, more particularly, it relates to a kind of terylene pre-tropism continuous yarn and manufacture method thereof.
Background technology
Along with improving constantly of social materials educational level, the requirement of people to clothing fabric, ornament materials is abundanter.Natural fabric and tModified Cellulose Fibers are no matter in output or can not meet the growing demand of people qualitatively.Therefore synthetic fiber technology is able to research and development widely, and chemical fibre, through the more function of modified imparting, instead of natural fabric gradually.And terylene is as first synthetic fiber, the multifunctional novel product of the applicable consumer demand of exploitation enjoys the concern of people.
Existing Authorization Notice No. is two-step method preparation technology and the polyester industrial yarn thereof that the Chinese patent of CN1321230C discloses a kind of HMLS terylene polyester industrial yarn, although its polyester industrial yarn prepared has the performance of HMLS terylene rate, its anti-ultraviolet property is bad.
Summary of the invention
For the deficiency that prior art exists, the object of the present invention is to provide a kind of terylene pre-tropism continuous yarn, there is good anti-ultraviolet property and higher fracture strength.
For achieving the above object, the invention provides following technical scheme:
A kind of terylene pre-tropism continuous yarn, in mass fraction, its raw material comprises: fiber level PET polyester sheet 90 ~ 100 parts, cetyl trimethyl silver bromide ammonium 0.1 ~ 0.5 part, 1,1 '-thiobis (beta naphthal) 1 ~ 1.3 part, 2-dihydroxy benaophenonel 0.7 ~ 1.2 part, 0.1 ~ 0.5 part, nickelous EDTA complex compound, preparation medium 2.7 ~ 3.2 parts.
Another object of the present invention is to provide the preparation method of terylene pre-tropism continuous yarn described above, comprise the steps:
Step 1) fiber level PET polyester sheet is cut into slices; It is dry that PET polyester slice carries out first time, and baking temperature is 160 ~ 180 DEG C, and drying time is 30min; It is dry that PET polyester slice carries out second time, and baking temperature is 185 DEG C, and drying time is 4 ~ 6 hours, makes the moisture content≤25ppm of PET polyester slice; PET polyester slice after drying carries out melting, cetyl trimethyl silver bromide ammonium, 1 is added after melting completely, 1 '-thiobis (beta naphthal), 2-dihydroxy benaophenonel, nickelous EDTA complex compound, evenly rear extruded one-tenth silk, cooling to be mixed;
Step 2) by step 1) in the PET Polyester Filament of gained carries out collecting through first roller successively, upper hot case heating, heater twisting, the second roller carry out stretching, lower hot case sizing, the 3rd roller are shaped further, oiling machine carries out refueling, take up roll shaping terylene pre-tropism continuous yarn; Wherein, fill preparation medium in described oiling machine, the speed of production controlling described terylene pre-tropism continuous yarn is 3300rad/min.
Step 1) described in section thickness be 0.5mm.
Step 1) described in the temperature of melting be 280 ~ 290 DEG C.
Step 1) described in cooling adopt ring quenching, wherein wind-warm syndrome is 18 ~ 22 DEG C, relative humidity is 70 ~ 80%, wind speed is 0.4 ~ 0.6m/s.
Step 2) described in the heating-up temperature of upper hot case sizing be 175 ~ 180 DEG C.
In step 1) in gained PET Polyester Filament after, directly carry out step 2) process.
Compared with prior art, the present invention has following beneficial effect:
(1) cetyl trimethyl silver bromide ammonium, silver ion is different with the Antibacterial Mechanism of quaternary ammonium salt, the Antibacterial Mechanism of silver ion is: because silver ion is positively charged, microorganism is generally electronegative, according to the effect of Coulomb attraction, both are attracting, when antimicrobial surface accumulates the anion of the concentration of some, anion just effectively can puncture the cell membrane of microorganism, and penetrate in microbial cell and react with the sulfydryl of protein, microprotein is solidified, protease inactivation, thus make microbial cell lose division, fertility, silver ion also has high reduction potential simultaneously, the space of surrounding can be made to produce elemental oxygen and greatly improve antibacterial effect, and the Antibacterial Mechanism of quaternary ammonium salt is Antibacterial Mechanism: quaternary ammonium salt progresses into cell by antimicrobial surface anion binding, destroys cell membrane, make cell content beyond the region of objective existence rush down and cause cell death, thus suppress microbial reproduction.It is unexpected that discovery cetyl trimethyl silver bromide ammonium can improve the fracture strength of pre-oriented yarn of the present invention, this may be due to degree of crystallinity when cetyl trimethyl silver bromide ammonium can improve spinning, improve the tightness of fibre structure, and then improve the fracture strength of pre-oriented yarn of the present invention.
(2) 1,1 '-thiobis (beta naphthal) is a kind of high-efficiency multi-function antioxidant; 2-dihydroxy benaophenonel is UV absorbers, containing o-hydroxy ketone group in its molecular structure, hydrogen bond ring can be formed in molecule, proton translocation is there is after molecule absorption ultraviolet is stimulated, and its molecule has high conjugated structure, can form resonance stable state, the molecule being in excited electronic state becomes vibrational excitation ground state by power conversion, restores to the original state with the form deactivation of heat release; Nickelous EDTA complex compound is quencher very effectively, can effectively cancellation excitation state carbonyl and singlet-oxygen quenching, and catches free radical; When 2-dihydroxy benaophenonel and nickelous EDTA complex compound share, synergy is produced to uvioresistant aspect, and 1,1 '-thiobis (beta naphthal) has the effect of enhancing to its synergy.
(3) fracture strength of production technology of the present invention to terylene pre-tropism continuous yarn has a great impact, and this all has influence on orientation and the crystallization of terylene pre-oriented fiber, thus the mechanical property of endowing terylene pre-oriented yarn.
Detailed description of the invention
Below the specific embodiment of the present invention is described in detail.Should be understood that, detailed description of the invention described herein, only for instruction and explanation of the present invention, is not limited to the present invention.
Embodiment 1
Step 1) fiber level PET polyester sheet 90Kg (polyethylene terephthalate plate, brand is German Gai Er) to be cut into slices, the thickness of section is 0.5mm; It is dry that PET polyester slice carries out first time, and baking temperature is 160 DEG C, and drying time is 30min; It is dry that PET polyester slice carries out second time, and baking temperature is 185 DEG C, and drying time is 4 hours, makes the moisture content≤25ppm of PET polyester slice; The cetyl trimethyl silver bromide ammonium of the PET polyester slice after drying and 0.2Kg, 1 of 1.1Kg, the 2-dihydroxy benaophenonel of 1 '-thiobis (beta naphthal), 0.7Kg, the nickelous EDTA complex compound of 0.5Kg fully mix in screw extruder, in 280 DEG C of meltings, extruded one-tenth silk, cooling, wherein cool that wind-warm syndrome is 20 DEG C, relative humidity 75%, wind speed 0.5m/s.
Step 2) by step 1) in the PET Polyester Filament of gained carries out collecting through first roller successively, the upper hot casees heating in 175 DEG C, heater twisting, the second roller carry out stretching, lower hot case sizing, the 3rd roller are shaped further, oiling machine carries out refueling, take up roll shaping terylene pre-tropism continuous yarn; Wherein, preparation medium (preparation medium is buied by Moraceae fibers material Products Co., Ltd of Zhongshan city, and oil applying rate is 3%, i.e. preparation medium 2.775Kg) is filled in described oiling machine,, the speed of production controlling described terylene pre-tropism continuous yarn is 3300rad/min.
Embodiment 2
The other the same as in Example 1, the irritated temperature of carrying out first time drying unlike PET polyester slice is 180 DEG C, and the drying time of second time drying is 6 hours, and melt temperature is 290 DEG C; Wind-warm syndrome during cooling is 18 DEG C, relative humidity is 70%, wind speed is 0.6m/s; The heating-up temperature of upper hot case sizing is 180 DEG C; Wherein its raw material comprises: fiber level PET polyester sheet 90Kg, cetyl trimethyl silver bromide ammonium 0.4Kg, 1,1 '-thiobis (beta naphthal) 1.3Kg, 2-dihydroxy benaophenonel 1.2Kg, nickelous EDTA complex compound 0.1Kg, preparation medium 3.2Kg.
Embodiment 3
The other the same as in Example 1, the irritated temperature of carrying out first time drying unlike PET polyester slice is 170 DEG C, and the drying time of second time drying is 5 hours, and melt temperature is 285 DEG C; Wind-warm syndrome during cooling is 22 DEG C, relative humidity is 80%, wind speed is 0.4m/s; The heating-up temperature of upper hot case sizing is 177 DEG C; Wherein its raw material comprises: fiber level PET polyester sheet 95Kg, cetyl trimethyl silver bromide ammonium (antiseptic) 0.5Kg, 1,1 '-thiobis (beta naphthal) (antioxidant) 1Kg, 2-dihydroxy benaophenonel (UV absorbers) 1Kg, nickelous EDTA complex compound (quencher) 0.3Kg, preparation medium 3Kg.
Embodiment 4
The other the same as in Example 1 is 288 DEG C unlike melt temperature; Wind-warm syndrome during cooling is 21 DEG C, relative humidity is 78%, wind speed is 0.5m/s; The heating-up temperature of upper hot case sizing is 177 DEG C; Wherein its raw material comprises: fiber level PET polyester sheet 97Kg, cetyl trimethyl silver bromide ammonium (antiseptic) 0.2Kg, 1,1 '-thiobis (beta naphthal) (antioxidant) 1.1Kg, 2-dihydroxy benaophenonel (UV absorbers) 1.1Kg, nickelous EDTA complex compound (quencher) 0.2Kg, preparation medium 2.9Kg.
Embodiment 5
The other the same as in Example 1, the irritated temperature of carrying out first time drying unlike PET polyester slice is 165 DEG C, and the drying time of second time drying is 5.5 hours, and melt temperature is 283 DEG C; Wind-warm syndrome during cooling is 19 DEG C, relative humidity is 75%, wind speed is 0.5m/s; The heating-up temperature of upper hot case sizing is 176 DEG C; Wherein its raw material comprises: fiber level PET polyester sheet 92Kg, cetyl trimethyl silver bromide ammonium (antiseptic) 0.3Kg, 1,1 '-thiobis (beta naphthal) (antioxidant) 1.3Kg, 2-dihydroxy benaophenonel (UV absorbers) 0.9Kg, nickelous EDTA complex compound (quencher) 0.3Kg, preparation medium 3.1Kg.
Comparative example 1
The other the same as in Example 1, dry unlike directly carrying out second time after the section of fiber level PET polyester sheet, save the technique of first time drying.
Comparative example 2
The other the same as in Example 1, unlike in step 1) in gained PET Polyester Filament after, after 30min, carry out step 2 again) process.
Comparative example 3
The other the same as in Example 1, unlike in step 1) do not add cetyl trimethyl silver bromide ammonium (antiseptic), but in step 2) in add preparation medium to.
Comparative example 4
The other the same as in Example 1, eliminate the technique that the 3rd roller is shaped further, direct oiling machine refuels.
In above-described embodiment and comparative example, the fracture strength of terylene pre-tropism continuous yarn according to GB/T16604-1996 in the powerful aircraft measurements of INSTRON-1122, rate of extension 500mm/min, sample clamping length 500mm.
Shrinkage factor measures according to GB/T16604-1996, external tension 0.5cN/Tex, at 177 DEG C of heat treatment 10min, measures the length variations of terylene pre-tropism continuous yarn, is calculated as follows out shrinkage factor:
Shrinkage factor=(initial sample length-sample final lengths)/initial sample length × 100%.
Extend stress corresponding when extending 5% when 5% stress refers to and utilizes INSTRON-1122 strength machine to measure fracture strength.
Terylene pre-tropism continuous yarn in table 1 above-described embodiment, after tested, its main performance index is as follows
Drawn by the data analysis in his-and-hers watches 1, the fracture strength of production technology of the present invention to terylene pre-tropism continuous yarn has a great impact, and this all has influence on orientation and the crystallization of terylene pre-oriented fiber, thus the mechanical property of endowing terylene pre-oriented yarn.(1) object that redrying is carried out in the section of fiber level PET polyester sheet is that to allow it carry out pre-crystallized, forms nucleus, strengthens induced crystallization effect; (2) in step 1) in gained PET Polyester Filament after, directly carry out step 2) the object of process be in order to uncrystallized polyethylene terephthalate is carried out recrystallization, improve close structure degree and the stability of terylene pre-oriented fiber further; (3) the interpolation opportunity of cetyl trimethyl silver bromide ammonium (antiseptic), add after melting, cetyl trimethyl silver bromide ammonium becomes out-phase nucleus, allows it shift to an earlier date crystallization, is released the effect playing antiseptic after the melting of cetyl trimethyl silver bromide; The object that (4) the 3rd rollers are shaped further is the degree of orientation improving terylene pre-oriented fiber.
Comparative example 5
The other the same as in Example 1, unlike not adding 2-dihydroxy benaophenonel (UV absorbers).
Comparative example 6
The other the same as in Example 1, unlike not adding nickelous EDTA complex compound (quencher).
Comparative example 7
The other the same as in Example 1, unlike there is no interpolation 1,1 '-thiobis (beta naphthal) (antioxidant).
Comparative example 8
Adopt the polyester industrial yarn that the two-step method preparation technology of Authorization Notice No. a kind of HMLS terylene polyester industrial yarn disclosed in the Chinese patent of CN1321230C manufactures.
The terylene pre-tropism continuous yarn obtained in embodiment 1 and comparative example 1 to 4 selects common plain weave to manufacture on ASL-2000 type rapier sample loom, and the tissue density of fabric is 260 × 190/10cm.Then adopt the antiultraviolet (UV) of Britain SDL company through and preventing coating protection test macro; according to AATCCTestMethod183-1998 testing standard, fabric is tested; each sample carries out 3 tests; angle is respectively 0 °, 45 ° and 90 °, obtains final UPF value after three times test value is average.
The anti-ultraviolet performance of table 2 fabric
Test event Embodiment 1 Comparative example 5 Comparative example 6 Comparative example 7 Comparative example 8
UPF value 60 10 5 25 11
Can be drawn by the data analysis of table 2: when 2-dihydroxy benaophenonel and nickelous EDTA complex compound share, synergy is produced to uvioresistant aspect, and 1,1 '-thiobis (beta naphthal) has the effect of enhancing to its synergy.
The above is only the preferred embodiment of the present invention; but the present invention is not limited to the detail in above-mentioned embodiment, within the scope of technical conceive of the present invention; can carry out multiple simple variant to technical scheme of the present invention, these simple variant all belong to protection domain of the present invention.

Claims (7)

1. a terylene pre-tropism continuous yarn, it is characterized in that, in mass fraction, its raw material comprises: fiber level PET polyester sheet 90 ~ 100 parts, cetyl trimethyl silver bromide ammonium (antiseptic) 0.1 ~ 0.5 part, 1,1 '-thiobis (beta naphthal) 1 ~ 1.3 part, 2-dihydroxy benaophenonel 0.7 ~ 1.2 part, 0.1 ~ 0.5 part, nickelous EDTA complex compound, preparation medium 2.7 ~ 3.2 parts.
2. the preparation method of terylene pre-tropism continuous yarn according to claim 1, is characterized in that, comprises the steps:
Step 1) fiber level PET polyester sheet is cut into slices; It is dry that PET polyester slice carries out first time, and baking temperature is 160 ~ 180 DEG C, and drying time is 30min; It is dry that PET polyester slice carries out second time, and baking temperature is 185 DEG C, and drying time is 4 ~ 6 hours, makes the moisture content≤25ppm of PET polyester slice; PET polyester slice after drying carries out melting, cetyl trimethyl silver bromide ammonium, 1 is added after melting completely, 1 '-thiobis (beta naphthal), 2-dihydroxy benaophenonel, nickelous EDTA complex compound, evenly rear extruded one-tenth silk, cooling to be mixed;
Step 2) by step 1) in the PET Polyester Filament of gained carries out collecting through first roller successively, upper hot case heating, heater twisting, the second roller carry out stretching, lower hot case sizing, the 3rd roller are shaped further, oiling machine carries out refueling, take up roll shaping terylene pre-tropism continuous yarn; Wherein, fill preparation medium in described oiling machine, the speed of production controlling described terylene pre-tropism continuous yarn is 3300rad/min.
3. the preparation method of terylene pre-tropism continuous yarn according to claim 2, is characterized in that, step 1) described in section thickness be 0.5mm.
4. the preparation method of terylene pre-tropism continuous yarn according to claim 2, is characterized in that, step 1) described in the temperature of melting be 280 ~ 290 DEG C.
5. the preparation method of terylene pre-tropism continuous yarn according to claim 2, is characterized in that, step 1) described in cooling adopt ring quenching, wherein wind-warm syndrome is 18 ~ 22 DEG C, relative humidity is 70 ~ 80%, wind speed is 0.4 ~ 0.6m/s.
6. the preparation method of terylene pre-tropism continuous yarn according to claim 2, is characterized in that, step 2) described in the heating-up temperature of upper hot case sizing be 175 ~ 180 DEG C.
7. the preparation method of terylene pre-tropism continuous yarn according to claim 2, is characterized in that, in step 1) in gained PET Polyester Filament after, directly carry out step 2) process.
CN201610014001.0A 2016-01-09 2016-01-09 Terylene pre-tropism continuous yarn and its manufacture method Active CN105420841B (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110699799A (en) * 2019-09-27 2020-01-17 浙江正堂实业股份有限公司 High-elastic polyester yarn and preparation method thereof
CN111485291A (en) * 2020-04-16 2020-08-04 莱芜富新纤维制品有限公司 Production process of polyester staple fiber
CN112281246A (en) * 2020-11-19 2021-01-29 湖州欣缘纺织有限公司 Preparation method of antistatic polyester filament yarn with good hydrophilicity
CN113004667A (en) * 2021-03-24 2021-06-22 北京悦康塑料制品有限公司 Complex plastic product and production process thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62223319A (en) * 1986-03-24 1987-10-01 Teijin Ltd Production of polyester fiber for hard twist yarn
JPH04281071A (en) * 1991-03-08 1992-10-06 Nippon Ester Co Ltd Production of polyester fiber
CN1464078A (en) * 2002-06-10 2003-12-31 中国石油化工股份有限公司 Process for manufacturing high modulus low retraction type trueran industrial filament and trueran industrial filament thereof
CN1537984A (en) * 2003-10-23 2004-10-20 王信友 Manufacturing method of high-modulus low-shrinking ferylene filament
CN101158054A (en) * 2007-08-09 2008-04-09 唐敏 Chromatic high-wet conductivity anti-bacterial fiber and spinning method thereof
CN101187087A (en) * 2007-11-28 2008-05-28 盛虹集团有限公司 Nanometer antibiotic ultra-fine polyester filament preparation method
CN102392317A (en) * 2011-09-07 2012-03-28 浙江三志纺织有限公司 Method for producing differential terylene color yarns

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62223319A (en) * 1986-03-24 1987-10-01 Teijin Ltd Production of polyester fiber for hard twist yarn
JPH04281071A (en) * 1991-03-08 1992-10-06 Nippon Ester Co Ltd Production of polyester fiber
CN1464078A (en) * 2002-06-10 2003-12-31 中国石油化工股份有限公司 Process for manufacturing high modulus low retraction type trueran industrial filament and trueran industrial filament thereof
CN1537984A (en) * 2003-10-23 2004-10-20 王信友 Manufacturing method of high-modulus low-shrinking ferylene filament
CN101158054A (en) * 2007-08-09 2008-04-09 唐敏 Chromatic high-wet conductivity anti-bacterial fiber and spinning method thereof
CN101187087A (en) * 2007-11-28 2008-05-28 盛虹集团有限公司 Nanometer antibiotic ultra-fine polyester filament preparation method
CN102392317A (en) * 2011-09-07 2012-03-28 浙江三志纺织有限公司 Method for producing differential terylene color yarns

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110699799A (en) * 2019-09-27 2020-01-17 浙江正堂实业股份有限公司 High-elastic polyester yarn and preparation method thereof
CN110699799B (en) * 2019-09-27 2021-03-02 浙江正堂实业股份有限公司 High-elastic polyester yarn and preparation method thereof
CN111485291A (en) * 2020-04-16 2020-08-04 莱芜富新纤维制品有限公司 Production process of polyester staple fiber
CN112281246A (en) * 2020-11-19 2021-01-29 湖州欣缘纺织有限公司 Preparation method of antistatic polyester filament yarn with good hydrophilicity
CN113004667A (en) * 2021-03-24 2021-06-22 北京悦康塑料制品有限公司 Complex plastic product and production process thereof

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