CN104294397B - Terylene has the manufacture craft of light abnormity half elastic force drafting - Google Patents

Terylene has the manufacture craft of light abnormity half elastic force drafting Download PDF

Info

Publication number
CN104294397B
CN104294397B CN201310299679.4A CN201310299679A CN104294397B CN 104294397 B CN104294397 B CN 104294397B CN 201310299679 A CN201310299679 A CN 201310299679A CN 104294397 B CN104294397 B CN 104294397B
Authority
CN
China
Prior art keywords
melt
minutes
elastic force
successively
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201310299679.4A
Other languages
Chinese (zh)
Other versions
CN104294397A (en
Inventor
左平安
陈阿斌
刘雪峰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujian Billion Polymerization Fiber Technology Industrial Co Ltd
Original Assignee
Fujian Billion Polymerization Fiber Technology Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fujian Billion Polymerization Fiber Technology Industrial Co Ltd filed Critical Fujian Billion Polymerization Fiber Technology Industrial Co Ltd
Priority to CN201310299679.4A priority Critical patent/CN104294397B/en
Publication of CN104294397A publication Critical patent/CN104294397A/en
Application granted granted Critical
Publication of CN104294397B publication Critical patent/CN104294397B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Artificial Filaments (AREA)

Abstract

The present invention relates to the manufacture craft that a kind of terylene has light abnormity half elastic force drafting, comprise from the preliminary treatment of polyester raw material low-shrinkage, high mould is blended light melt treatment, the multistage straight melt-spun silk of melt, filter screen spray silk cools the oil particular design of half elastic force stretch processing processing step and the special optimization of relevant parameter, form the manufacture craft that a kind of terylene has light abnormity half elastic force drafting, solve the deficiency that gloss and elasticity drawing-off performance in prior art are lower, achieve it in anaclasis, reflection, percent thermal shrinkage, and half elasticity, drawing-off, flexible texture, gloss, the effect that low elasticity aspect performance is more excellent.

Description

Terylene has the manufacture craft of light abnormity half elastic force drafting
Technical field
The present invention relates to the manufacture technology field of drafting, particularly relate to a kind of manufacture craft of special-shaped half elastic force drafting, relate to the manufacture craft that a kind of terylene has light abnormity half elastic force drafting in particular.
Background technology
Ultra-coarse denier lustrous terylene drawn yarn adopt by p-phthalic acid's (be called for short PTA), ethylene glycol (abbreviated as MEG) be polymerized make have light directly to spin melt to be raw material, to be made by the operation such as spinning, stretching.In current chemical fibre industry, the line density of polyester drawn yarns the most only can reach for 300 dawn, its production technology is: with PTA, what MEG polymerization was made has light directly to spin melt is raw material, after booster pump supercharging, spinning manifold is sent into by melt Conveying pipeline, and through measuring pump accurate measurement, melt shape fiber is formed after the filament spinning component in spinning manifold filters, as-spun fibre is become again through lateral blowing cooling curing, again after oil tanker oils, again through the first draw-off godet hot-rolling, second spinning reel hot-rolling carries out stretching HEAT SETTING, then by thread guide polyster fibre line is merged into and has light polyester drawn yarns about 300 dawn, finally will there is light polyester drawn yarns package build by winding head.The shortcoming of above-mentioned preparation method is: in production technology, the later stage of three leaf odd-shaped cross section lustrous fibre lines merges, and makes to lack cohesive force between monofilament, easily diverges in the use procedure of rear road; Monofilament cohesive force is uneven, and during stretching, between monofilament, tension force differs, three leaf abnormity have light easily to produce boundling is irregular, single wire fracture forms lousiness, thus after impact, road is weaved and the flatness of cloth cover, cannot reach the aft-loaded airfoil requirement of coarse denier fiber; And the polyester drawn yarns that conventional spinning obtains the most only can reach for 300 dawn, and range of application is restricted.
Nearest Two decades years comes, for improving polyester fiber moisture absorption, water vapour permeability, do a lot of work in Japan and Taiwan, according to patent report in the past, occurred two research peak periods, first research peak period is-1986 years nineteen eighty-twos, mainly with polymerization methods synthetic copolyester during this, then direct copolyesters carries out spinning, or by copolyesters and conventional polyester mixing after carry out spinning again; Second research peak period is nineteen ninety-five, mainly to synthesize batching or to add hole plasticizer in mixing mode, then via alkali treatment processing, makes fiber produce hole.
As Japanese Di Ren company released hollow micro-porous fibre first generation product patent in 1986, its commodity are called WellkeyFilament, its preparation is the microphase-separated principle utilizing conventional polyester and hole plasticizer, then after making high oriented yarn HOY (Highlyorientedyarn) via high-speed spinning, then give suitable alkali treatment and be prepared from.Japanese Di Ren company also utilizes unique chemical method simultaneously, by a kind of silk-fibroin of high-absorbency material, be coated on hygroscopicity fibre, develop " moisture-absorbing fibre ", this kind of fiber called after WellkeyMA fiber, the absorbing sweat/fast dry characteristic of its fabric, than strong ten times, conventional polyester fabric, but its hollow rate is not high, between 5-10%.In addition, the nineties in 20th century is developed the dry and comfortable fiber of the many micropores of hollow, trade (brand) name Hydropre at the Industrial Technology Research Institute of Taiwan's chemical industry place, and it adopts special spinning process, allows the inside and outside tube wall of fiber all have elongated groove, by these grooves and hole moisture absorption, moisture-inhibiting.But polyester fiber only has moisture absorption, moisture permeable effect is far from being enough.Above-described all patents only improve emphatically the moisture absorption of polyester fiber, ventilative, comfort type, do not improve other functions of fiber further.Certainly, the many microporous fibres of hollow are owing to preparing burden or pore former owing to having copolyesters or synthesizing, and spinning technique difficulty controls, and finished silk intensity reduces, takes easy fibrillation in process, functional after-finishing not easily carries out, and before fibroblast, give functional form also certainly will be more difficult.
Along with the raising of people's living standard, various comfortableness, health functional fibre emerge in an endless stream.So can produce and both there is moisture absorption, moisture permeable effect, there is there again the fiber of manifest function health properties? first, because the many microporous fibres of hollow are inherently wayward by hollow type spinnerets spinning technique by two kinds of component slices, moreover after adding function modified master batch, require stricter to spinning and aftertreatment technology.At present, there is no the report of this respect both at home and abroad.
Terylene as one of the large main force of three in synthetic fiber fiber, because its excellent physics and chemistry characteristic is widely used in garment material and other non-garment industry.Dacron product since appearance, also once so that its drapability is good, intensity is high, well-pressed and be used as main textile raw material to weave all kinds of textiles by downstream user.Along with economic globalization, internationalizationof of market, the requirement of people to clothes is also more and more higher, not only comfortableness will be had, also will have functional, fabric is just to light, soft, functional future development, and composite fibre materials just needs to improve constantly performance to meet requirements of weaving process.
Nearly ten years, the development of China polyester industrial rapidly, polyester fiber output from 516.5 at the beginning of 2000 ten thousand tons develop into ten thousand tons, 2700 at the end of 2010, average annual growth rate, more than 25%, has accounted for 66% of global polyester output.Terylene has become the maximum synthetic fiber kind of output in chemical fibre, is widely used in clothing, decoration, household textiles, fabrics for industrial use and the national economy such as national defence, Industrial Engineering various aspects.5 years from now on, also will keep increasing fast.But as textile material, polyester fiber also has obvious shortcoming.Therefore, the processing method of science, efficient, high-quality, energy-saving and environmental protection is selected, to adapting to and promoting that the high speed sustainable development of polyester industrial, polyster fibre is most important.
Although in synthetic fiber, polyester fiber has the multiple performance of applicable textile applications and industry application, and thus it has achieved the development attracted people's attention since large-scale production.But along with the progress of World Science technology and the development of world industry, polyester fiber is in performance and the requirement that functionally can not meet people completely.The result of development and innovation makes to be developed large quantities of differential, functionalization and high performance synthetic fiber.
Due to " small-size effect ", " interfacial effect ", " quantum size effect " and " macro quanta tunnel effect " that nano material has, nano material is made to show the specificity different from common material in structure, photoelectricity, magnetic and chemical property etc.
Full-drawn yarn adopts low speed spinning, high-speed stretch technique, and two procedures is on a spin-drawing combination machine, for one-step technology route, spinning speed is 900-1500m/min, stretching and winding speed is 3200-4200m/min, draw ratio is about 3.5, and full-drawn yarn has the more stable feature of quality.
Present inventor is devoted to material modification to have in light abnormity half elastic force drafting at terylene to transform, and subsequent treatment carries out particular design, and completes the present invention in conjunction with full-drawn yarn production technology of the prior art.
Summary of the invention
The object of the invention is for above-mentioned deficiency, there is provided a kind of from a series of particular design of strong reflecting low-stretch yarn step of preparation process and the special optimization of relevant parameter such as raw material preparation, material modification preliminary treatment, spinning, post processings, form the manufacture craft that a kind of terylene has light abnormity half elastic force drafting, reach it in anaclasis, reflection, percent thermal shrinkage and half elasticity, drawing-off, flexible texture, gloss, the effect that low elasticity aspect performance is more excellent.
For achieving the above object, the present invention is achieved by the following technical solutions:
A kind of terylene of the present invention has the manufacture craft of light abnormity half elastic force drafting, it is characterized in that, this terylene has the manufacture craft of light abnormity half elastic force drafting to comprise successively: the preliminary treatment of polyester raw material low-shrinkage, high mould be blended to be had the multistage straight melt-spun silk of light melt treatment, melt, filter screen to spray silk cooling to oil half elastic force stretch processing.
Wherein:
The preliminary treatment of described polyester raw material low-shrinkage comprises esterification process and polymerisation process, described esterification process: by 1, ammediol, ethylene glycol, phthalic acid, terephthalic acid (TPA) adds in sealing esterification ware according to mol ratio 12:7:4:11, described sealing esterification ware is built-in with and carries out stirring low-frequency oscillation instrument and infrared heating pipeline, described infrared heating pipeline keeps described sealing esterification utensil temperature to control to continue 55 minutes within the scope of 225 ~ 234 DEG C, and then add micro-potassium antimonate fine catalyst again continue within 35 ~ 45 minutes, fully carry out esterification, wherein said potassium antimonate powder weight account for described 1,3-PD, ethylene glycol, phthalic acid, terephthalic acid (TPA) amount of the mixture 0.01 ~ 0.03%, described polymerisation process: the polymerization single polymerization monomer above-mentioned esterification obtained carries out high temperature polymerization under the existence of polymerization catalyst and defoamer, then the polymer after polymerization is obtained polymer chips through pelletizing, the temperature of wherein said high temperature polymerization is 323 ~ 325 DEG C, before polymerisation is carried out, add the methylcellulose nano particle accounting for described polymer chips gross weight 0.002 ~ 0.005% in described polymerization single polymerization monomer, described methylcellulose nano particle joins in described polymerization single polymerization monomer with homodisperse form,
Described high mould is blended light melt treatment: added successively by the above-mentioned polymer chips that above-mentioned polymerisation process obtains in two rotation batch mixing vacuum reaction cylinders and carry out the process of high mould blended melting; Wherein, by above-mentioned polymer chips and flux according to weight ratio 16:0.3, add first rotation batch mixing vacuum reaction cylinder, initial temperature is 145 DEG C, then with the temperature rate of 0.5 DEG C/min, keep 55 ~ 65 minutes after being at the uniform velocity increased to 275 DEG C, the rotary speed of described first rotation batch mixing vacuum reaction cylinder is 65 ~ 75 revs/min; Then at the uniform velocity being joined via S shape melt canal by the molten mixture of described first rotation batch mixing vacuum reaction cylinder is built-in with in second rotation batch mixing vacuum reaction cylinder of optical brightener, the rotary speed of described second rotation batch mixing vacuum reaction cylinder at the uniform velocity remains on 224 ~ 226 revs/min all the time, when being at the uniform velocity increased to 262 DEG C with the temperature rate of 1.2 DEG C/min from 22 DEG C, keep 12 ~ 16 minutes; Wherein, described flux be albite, hydroxypropyl cellulose, isobutanol, ethyl cellulose according to weight portion 2 parts, 5 parts, 3 parts, 7 parts, at temperature 187 DEG C, Homogeneous phase mixing is after 92 ~ 95 minutes, is at the uniform velocity cooled to 65 DEG C and the mixture obtained after keeping 13 ~ 16 minutes; Described optical brightener be dodecyl semi-annular jade pendant acid sodium, silicone oil, trimethyl phosphate, butyl titanate according to weight portion 11 parts, 3 parts, 9 parts, 7 parts, at temperature 105 DEG C, Homogeneous phase mixing is after 35 ~ 40 minutes, is at the uniform velocity cooled to 35 DEG C and the mixture obtained after keeping 85 minutes;
The multistage straight melt-spun silk of described melt: have the homogeneous fused mass of light melt treatment to be injected in real time in twin (double) screw extruder by S shape injection-tube by blended for above-mentioned high mould, wherein, the screw extruding melting pipeline of described twin (double) screw extruder is divided into five melting zones successively, first melting zone and the 5th melting zone are low temperature 164 ~ 168 DEG C, keep 95 minutes; Second melting zone and the 4th melting zone, all from initial 232 ~ 234 DEG C, after being increased to 255 ~ 258 DEG C, keep 20 ~ 25 minutes with the speed of 0.5 DEG C/min; 3rd melting zone, from initial 255 ~ 258 DEG C, with behind rate reduction to 165 ~ 168 of 0.25 DEG C/min DEG C, keeps 75 minutes;
The cooling of described filter screen spray silk oils half elastic force stretch processing: by multistage for described melt straight melt-spun silk via the homogeneous fused mass after twin (double) screw extruder, enter back taper fondant filter, built-in three the parallel filter nets of described back taper fondant filter, described three parallel filter nets from top to bottom mesh diminish successively, spinning pump accurate measurement is delivered to by melt distributing pipe after filtration, the nascent strand of ejection in the special-shaped composite component be incubated by spinning manifold is accordingly evenly distributed to by multiple isometric S shape melt pipe, cooling forming is carried out successively again through ring blowing device, oil nozzle oils, then drawing and heat-setting is carried out, then described nascent strand is more successively after multiple tracks tension rollers and multiple pre-Network device, again after the control roll that three road tension force successively decrease successively, enter the draw zone being provided with three groups of drawing-off hot-rollings again and carry out share split drawing-off, again after six groups of sizing hot-rolling share split HEAT SETTING of symmetry, plying enters master network device and carries out network processes, then coiling and molding is carried out via up-coiler.
Beneficial effect: the present invention is except the said goods performance, simple for process, processing cost is low, parameter optimization, thus makes constant product quality, bar is evenly dry, and filoplume rate is low, and Color is good, good mechanical performance.
Detailed description of the invention
Below in conjunction with detailed description of the invention, set forth the present invention further.
Embodiment 1:
A kind of terylene has the manufacture craft of light abnormity half elastic force drafting, it is characterized in that, this terylene has the manufacture craft of light abnormity half elastic force drafting to comprise successively: the preliminary treatment of polyester raw material low-shrinkage, high mould be blended to be had the multistage straight melt-spun silk of light melt treatment, melt, filter screen to spray silk cooling to oil half elastic force stretch processing.
Embodiment 2:
A kind of terylene has the manufacture craft of light abnormity half elastic force drafting, it is characterized in that, this terylene has the manufacture craft of light abnormity half elastic force drafting to comprise successively: the preliminary treatment of polyester raw material low-shrinkage, high mould be blended to be had the multistage straight melt-spun silk of light melt treatment, melt, filter screen to spray silk cooling to oil half elastic force stretch processing, the preliminary treatment of described polyester raw material low-shrinkage comprises esterification process and polymerisation process, described esterification process: by 1, ammediol, ethylene glycol, phthalic acid, terephthalic acid (TPA) adds in sealing esterification ware according to mol ratio 12:7:4:11, described sealing esterification ware is built-in with and carries out stirring low-frequency oscillation instrument and infrared heating pipeline, described infrared heating pipeline keeps described sealing esterification utensil temperature to control to continue 55 minutes within the scope of 225 ~ 234 DEG C, and then add micro-potassium antimonate fine catalyst again continue within 35 ~ 45 minutes, fully carry out esterification, wherein said potassium antimonate powder weight account for described 1,3-PD, ethylene glycol, phthalic acid, terephthalic acid (TPA) amount of the mixture 0.01 ~ 0.03%, described polymerisation process: the polymerization single polymerization monomer above-mentioned esterification obtained carries out high temperature polymerization under the existence of polymerization catalyst and defoamer, then the polymer after polymerization is obtained polymer chips through pelletizing, the temperature of wherein said high temperature polymerization is 323 ~ 325 DEG C, before polymerisation is carried out, add the methylcellulose nano particle accounting for described polymer chips gross weight 0.002 ~ 0.005% in described polymerization single polymerization monomer, described methylcellulose nano particle joins in described polymerization single polymerization monomer with homodisperse form,
Described high mould is blended light melt treatment: added successively by the above-mentioned polymer chips that above-mentioned polymerisation process obtains in two rotation batch mixing vacuum reaction cylinders and carry out the process of high mould blended melting; Wherein, by above-mentioned polymer chips and flux according to weight ratio 16:0.3, add first rotation batch mixing vacuum reaction cylinder, initial temperature is 145 DEG C, then with the temperature rate of 0.5 DEG C/min, keep 55 ~ 65 minutes after being at the uniform velocity increased to 275 DEG C, the rotary speed of described first rotation batch mixing vacuum reaction cylinder is 65 ~ 75 revs/min; Then at the uniform velocity being joined via S shape melt canal by the molten mixture of described first rotation batch mixing vacuum reaction cylinder is built-in with in second rotation batch mixing vacuum reaction cylinder of optical brightener, the rotary speed of described second rotation batch mixing vacuum reaction cylinder at the uniform velocity remains on 224 ~ 226 revs/min all the time, when being at the uniform velocity increased to 262 DEG C with the temperature rate of 1.2 DEG C/min from 22 DEG C, keep 12 ~ 16 minutes; Wherein, described flux be albite, hydroxypropyl cellulose, isobutanol, ethyl cellulose according to weight portion 2 parts, 5 parts, 3 parts, 7 parts, at temperature 187 DEG C, Homogeneous phase mixing is after 92 ~ 95 minutes, is at the uniform velocity cooled to 65 DEG C and the mixture obtained after keeping 13 ~ 16 minutes; Described optical brightener be dodecyl semi-annular jade pendant acid sodium, silicone oil, trimethyl phosphate, butyl titanate according to weight portion 11 parts, 3 parts, 9 parts, 7 parts, at temperature 105 DEG C, Homogeneous phase mixing is after 35 ~ 40 minutes, is at the uniform velocity cooled to 35 DEG C and the mixture obtained after keeping 85 minutes;
The multistage straight melt-spun silk of described melt: have the homogeneous fused mass of light melt treatment to be injected in real time in twin (double) screw extruder by S shape injection-tube by blended for above-mentioned high mould, wherein, the screw extruding melting pipeline of described twin (double) screw extruder is divided into five melting zones successively, first melting zone and the 5th melting zone are low temperature 164 ~ 168 DEG C, keep 95 minutes; Second melting zone and the 4th melting zone, all from initial 232 ~ 234 DEG C, after being increased to 255 ~ 258 DEG C, keep 20 ~ 25 minutes with the speed of 0.5 DEG C/min; 3rd melting zone, from initial 255 ~ 258 DEG C, with behind rate reduction to 165 ~ 168 of 0.25 DEG C/min DEG C, keeps 75 minutes;
The cooling of described filter screen spray silk oils half elastic force stretch processing: by multistage for described melt straight melt-spun silk via the homogeneous fused mass after twin (double) screw extruder, enter back taper fondant filter, built-in three the parallel filter nets of described back taper fondant filter, described three parallel filter nets from top to bottom mesh diminish successively, spinning pump accurate measurement is delivered to by melt distributing pipe after filtration, the nascent strand of ejection in the special-shaped composite component be incubated by spinning manifold is accordingly evenly distributed to by multiple isometric S shape melt pipe, cooling forming is carried out successively again through ring blowing device, oil nozzle oils, then drawing and heat-setting is carried out, then described nascent strand is more successively after multiple tracks tension rollers and multiple pre-Network device, again after the control roll that three road tension force successively decrease successively, enter the draw zone being provided with three groups of drawing-off hot-rollings again and carry out share split drawing-off, again after six groups of sizing hot-rolling share split HEAT SETTING of symmetry, plying enters master network device and carries out network processes, then coiling and molding is carried out via up-coiler.
Embodiment 3:
A kind of terylene has the manufacture craft of light abnormity half elastic force drafting, it is characterized in that, this terylene has the manufacture craft of light abnormity half elastic force drafting to comprise successively: the preliminary treatment of polyester raw material low-shrinkage, high mould be blended to be had the multistage straight melt-spun silk of light melt treatment, melt, filter screen to spray silk cooling to oil half elastic force stretch processing, the preliminary treatment of described polyester raw material low-shrinkage comprises esterification process and polymerisation process, described esterification process: by 1, ammediol, ethylene glycol, phthalic acid, terephthalic acid (TPA) adds in sealing esterification ware according to mol ratio 12:7:4:11, described sealing esterification ware is built-in with and carries out stirring low-frequency oscillation instrument and infrared heating pipeline, described infrared heating pipeline keeps described sealing esterification utensil temperature to control to continue 55 minutes within the scope of 225 ~ 234 DEG C, and then add micro-potassium antimonate fine catalyst again continue within 35 ~ 45 minutes, fully carry out esterification, wherein said potassium antimonate powder weight account for described 1,3-PD, ethylene glycol, phthalic acid, terephthalic acid (TPA) amount of the mixture 0.02%, described polymerisation process: the polymerization single polymerization monomer above-mentioned esterification obtained carries out high temperature polymerization under the existence of polymerization catalyst and defoamer, then the polymer after polymerization is obtained polymer chips through pelletizing, the temperature of wherein said high temperature polymerization is 323 ~ 325 DEG C, before polymerisation is carried out, add the methylcellulose nano particle accounting for described polymer chips gross weight 0.002 ~ 0.005% in described polymerization single polymerization monomer, described methylcellulose nano particle joins in described polymerization single polymerization monomer with homodisperse form,
Described high mould is blended light melt treatment: added successively by the above-mentioned polymer chips that above-mentioned polymerisation process obtains in two rotation batch mixing vacuum reaction cylinders and carry out the process of high mould blended melting; Wherein, by above-mentioned polymer chips and flux according to weight ratio 16:0.3, add first rotation batch mixing vacuum reaction cylinder, initial temperature is 145 DEG C, then with the temperature rate of 0.5 DEG C/min, keep 55 ~ 65 minutes after being at the uniform velocity increased to 275 DEG C, the rotary speed of described first rotation batch mixing vacuum reaction cylinder is 65 ~ 75 revs/min; Then at the uniform velocity being joined via S shape melt canal by the molten mixture of described first rotation batch mixing vacuum reaction cylinder is built-in with in second rotation batch mixing vacuum reaction cylinder of optical brightener, the rotary speed of described second rotation batch mixing vacuum reaction cylinder at the uniform velocity remains on 224 ~ 226 revs/min all the time, when being at the uniform velocity increased to 262 DEG C with the temperature rate of 1.2 DEG C/min from 22 DEG C, keep 12 ~ 16 minutes; Wherein, described flux be albite, hydroxypropyl cellulose, isobutanol, ethyl cellulose according to weight portion 2 parts, 5 parts, 3 parts, 7 parts, at temperature 187 DEG C, Homogeneous phase mixing is after 92 ~ 95 minutes, is at the uniform velocity cooled to 65 DEG C and the mixture obtained after keeping 13 ~ 16 minutes; Described optical brightener be dodecyl semi-annular jade pendant acid sodium, silicone oil, trimethyl phosphate, butyl titanate according to weight portion 11 parts, 3 parts, 9 parts, 7 parts, at temperature 105 DEG C, Homogeneous phase mixing is after 35 ~ 40 minutes, is at the uniform velocity cooled to 35 DEG C and the mixture obtained after keeping 85 minutes;
The multistage straight melt-spun silk of described melt: have the homogeneous fused mass of light melt treatment to be injected in real time in twin (double) screw extruder by S shape injection-tube by blended for above-mentioned high mould, wherein, the screw extruding melting pipeline of described twin (double) screw extruder is divided into five melting zones successively, first melting zone and the 5th melting zone are low temperature 164 ~ 168 DEG C, keep 95 minutes; Second melting zone and the 4th melting zone, all from initial 232 ~ 234 DEG C, after being increased to 255 ~ 258 DEG C, keep 20 ~ 25 minutes with the speed of 0.5 DEG C/min; 3rd melting zone, from initial 257 DEG C, with after the rate reduction to 167 of 0.25 DEG C/min DEG C, keeps 75 minutes;
The cooling of described filter screen spray silk oils half elastic force stretch processing: by multistage for described melt straight melt-spun silk via the homogeneous fused mass after twin (double) screw extruder, enter back taper fondant filter, built-in three the parallel filter nets of described back taper fondant filter, described three parallel filter nets from top to bottom mesh diminish successively, spinning pump accurate measurement is delivered to by melt distributing pipe after filtration, the nascent strand of ejection in the special-shaped composite component be incubated by spinning manifold is accordingly evenly distributed to by multiple isometric S shape melt pipe, cooling forming is carried out successively again through ring blowing device, oil nozzle oils, then drawing and heat-setting is carried out, then described nascent strand is more successively after multiple tracks tension rollers and multiple pre-Network device, again after the control roll that three road tension force successively decrease successively, enter the draw zone being provided with three groups of drawing-off hot-rollings again and carry out share split drawing-off, again after six groups of sizing hot-rolling share split HEAT SETTING of symmetry, plying enters master network device and carries out network processes, then coiling and molding is carried out via up-coiler.
Embodiment 4:
A kind of terylene has the manufacture craft of light abnormity half elastic force drafting, it is characterized in that, this terylene has the manufacture craft of light abnormity half elastic force drafting to comprise successively: the preliminary treatment of polyester raw material low-shrinkage, high mould be blended to be had the multistage straight melt-spun silk of light melt treatment, melt, filter screen to spray silk cooling to oil half elastic force stretch processing, the preliminary treatment of described polyester raw material low-shrinkage comprises esterification process and polymerisation process, described esterification process: by 1, ammediol, ethylene glycol, phthalic acid, terephthalic acid (TPA) adds in sealing esterification ware according to mol ratio 12:7:4:11, described sealing esterification ware is built-in with and carries out stirring low-frequency oscillation instrument and infrared heating pipeline, described infrared heating pipeline keeps described sealing esterification utensil temperature to control to continue 55 minutes within the scope of 225 ~ 234 DEG C, and then add micro-potassium antimonate fine catalyst again continue within 39.5 minutes, fully carry out esterification, wherein said potassium antimonate powder weight account for described 1,3-PD, ethylene glycol, phthalic acid, terephthalic acid (TPA) amount of the mixture 0.02%, described polymerisation process: the polymerization single polymerization monomer above-mentioned esterification obtained carries out high temperature polymerization under the existence of polymerization catalyst and defoamer, then the polymer after polymerization is obtained polymer chips through pelletizing, the temperature of wherein said high temperature polymerization is 323 ~ 325 DEG C, before polymerisation is carried out, add the methylcellulose nano particle accounting for described polymer chips gross weight 0.002 ~ 0.005% in described polymerization single polymerization monomer, described methylcellulose nano particle joins in described polymerization single polymerization monomer with homodisperse form,
Described high mould is blended light melt treatment: added successively by the above-mentioned polymer chips that above-mentioned polymerisation process obtains in two rotation batch mixing vacuum reaction cylinders and carry out the process of high mould blended melting; Wherein, by above-mentioned polymer chips and flux according to weight ratio 16:0.3, add first rotation batch mixing vacuum reaction cylinder, initial temperature is 145 DEG C, then with the temperature rate of 0.5 DEG C/min, keep 55 ~ 65 minutes after being at the uniform velocity increased to 275 DEG C, the rotary speed of described first rotation batch mixing vacuum reaction cylinder is 65 ~ 75 revs/min; Then at the uniform velocity being joined via S shape melt canal by the molten mixture of described first rotation batch mixing vacuum reaction cylinder is built-in with in second rotation batch mixing vacuum reaction cylinder of optical brightener, the rotary speed of described second rotation batch mixing vacuum reaction cylinder at the uniform velocity remains on 224 ~ 226 revs/min all the time, when being at the uniform velocity increased to 262 DEG C with the temperature rate of 1.2 DEG C/min from 22 DEG C, keep 12 ~ 16 minutes; Wherein, described flux be albite, hydroxypropyl cellulose, isobutanol, ethyl cellulose according to weight portion 2 parts, 5 parts, 3 parts, 7 parts, at temperature 187 DEG C, Homogeneous phase mixing is after 92 ~ 95 minutes, is at the uniform velocity cooled to 65 DEG C and the mixture obtained after keeping 13 ~ 16 minutes; Described optical brightener be dodecyl semi-annular jade pendant acid sodium, silicone oil, trimethyl phosphate, butyl titanate according to weight portion 11 parts, 3 parts, 9 parts, 7 parts, at temperature 105 DEG C, Homogeneous phase mixing is after 35 ~ 40 minutes, is at the uniform velocity cooled to 35 DEG C and the mixture obtained after keeping 85 minutes;
The multistage straight melt-spun silk of described melt: have the homogeneous fused mass of light melt treatment to be injected in real time in twin (double) screw extruder by S shape injection-tube by blended for above-mentioned high mould, wherein, the screw extruding melting pipeline of described twin (double) screw extruder is divided into five melting zones successively, first melting zone and the 5th melting zone are low temperature 164 ~ 168 DEG C, keep 95 minutes; Second melting zone and the 4th melting zone, all from initial 232 ~ 234 DEG C, after being increased to 255 ~ 258 DEG C, keep 20 ~ 25 minutes with the speed of 0.5 DEG C/min; 3rd melting zone, from initial 255 ~ 258 DEG C, with behind rate reduction to 165 ~ 168 of 0.25 DEG C/min DEG C, keeps 75 minutes;
The cooling of described filter screen spray silk oils half elastic force stretch processing: by multistage for described melt straight melt-spun silk via the homogeneous fused mass after twin (double) screw extruder, enter back taper fondant filter, built-in three the parallel filter nets of described back taper fondant filter, described three parallel filter nets from top to bottom mesh diminish successively, spinning pump accurate measurement is delivered to by melt distributing pipe after filtration, the nascent strand of ejection in the special-shaped composite component be incubated by spinning manifold is accordingly evenly distributed to by multiple isometric S shape melt pipe, cooling forming is carried out successively again through ring blowing device, oil nozzle oils, then drawing and heat-setting is carried out, then described nascent strand is more successively after multiple tracks tension rollers and multiple pre-Network device, again after the control roll that three road tension force successively decrease successively, enter the draw zone being provided with three groups of drawing-off hot-rollings again and carry out share split drawing-off, again after six groups of sizing hot-rolling share split HEAT SETTING of symmetry, plying enters master network device and carries out network processes, then coiling and molding is carried out via up-coiler.
The present invention is not limited to above-mentioned specific embodiment, and do not deviating under the present invention's spirit and real situation thereof, those of ordinary skill in the art can make various corresponding change and distortion according to the present invention.These corresponding changes and distortion all should belong within the protection domain of claims of the present invention.

Claims (1)

1. a terylene has the manufacture craft of light abnormity half elastic force drafting, it is characterized in that, this terylene has the manufacture craft of light abnormity half elastic force drafting to comprise successively: the preliminary treatment of polyester raw material low-shrinkage, high mould be blended to be had the multistage straight melt-spun silk of light melt treatment, melt, filter screen to spray silk cooling to oil half elastic force stretch processing;
The preliminary treatment of described polyester raw material low-shrinkage comprises esterification process and polymerisation process, described esterification process: by 1, ammediol, ethylene glycol, phthalic acid, terephthalic acid (TPA) adds in sealing esterification ware according to mol ratio 12:7:4:11, described sealing esterification ware is built-in with and carries out stirring low-frequency oscillation instrument and infrared heating pipeline, described infrared heating pipeline keeps described sealing esterification utensil temperature to control to continue 55 minutes within the scope of 225 ~ 234 DEG C, and then add micro-potassium antimonate fine catalyst again continue within 35 ~ 45 minutes, fully carry out esterification, wherein said potassium antimonate powder weight account for described 1,3-PD, ethylene glycol, phthalic acid, terephthalic acid (TPA) amount of the mixture 0.01 ~ 0.03%, described polymerisation process: the polymerization single polymerization monomer above-mentioned esterification obtained carries out high temperature polymerization under the existence of polymerization catalyst and defoamer, then the polymer after polymerization is obtained polymer chips through pelletizing, the temperature of wherein said high temperature polymerization is 323 ~ 325 DEG C, before polymerisation is carried out, add the methylcellulose nano particle accounting for described polymer chips gross weight 0.002 ~ 0.005% in described polymerization single polymerization monomer, described methylcellulose nano particle joins in described polymerization single polymerization monomer with homodisperse form,
Described high mould is blended light melt treatment: added successively by the above-mentioned polymer chips that above-mentioned polymerisation process obtains in two rotation batch mixing vacuum reaction cylinders and carry out the process of high mould blended melting; Wherein, by above-mentioned polymer chips and flux according to weight ratio 16:0.3, add first rotation batch mixing vacuum reaction cylinder, initial temperature is 145 DEG C, then with the temperature rate of 0.5 DEG C/min, keep 55 ~ 65 minutes after being at the uniform velocity increased to 275 DEG C, the rotary speed of described first rotation batch mixing vacuum reaction cylinder is 65 ~ 75 revs/min; Then at the uniform velocity being joined via S shape melt canal by the molten mixture of described first rotation batch mixing vacuum reaction cylinder is built-in with in second rotation batch mixing vacuum reaction cylinder of optical brightener, the rotary speed of described second rotation batch mixing vacuum reaction cylinder at the uniform velocity remains on 224 ~ 226 revs/min all the time, when being at the uniform velocity increased to 262 DEG C with the temperature rate of 1.2 DEG C/min from 22 DEG C, keep 12 ~ 16 minutes; Wherein, described flux be albite, hydroxypropyl cellulose, isobutanol, ethyl cellulose according to weight portion 2 parts, 5 parts, 3 parts, 7 parts, at temperature 187 DEG C, Homogeneous phase mixing is after 92 ~ 95 minutes, is at the uniform velocity cooled to 65 DEG C and the mixture obtained after keeping 13 ~ 16 minutes; Described optical brightener be dodecyl semi-annular jade pendant acid sodium, silicone oil, trimethyl phosphate, butyl titanate according to weight portion 11 parts, 3 parts, 9 parts, 7 parts, at temperature 105 DEG C, Homogeneous phase mixing is after 35 ~ 40 minutes, is at the uniform velocity cooled to 35 DEG C and the mixture obtained after keeping 85 minutes;
The multistage straight melt-spun silk of described melt: have the homogeneous fused mass of light melt treatment to be injected in real time in twin (double) screw extruder by S shape injection-tube by blended for above-mentioned high mould, wherein, the screw extruding melting pipeline of described twin (double) screw extruder is divided into five melting zones successively, first melting zone and the 5th melting zone are low temperature 164 ~ 168 DEG C, keep 95 minutes; Second melting zone and the 4th melting zone, all from initial 232 ~ 234 DEG C, after being increased to 255 ~ 258 DEG C, keep 20 ~ 25 minutes with the speed of 0.5 DEG C/min; 3rd melting zone, from initial 255 ~ 258 DEG C, with behind rate reduction to 165 ~ 168 of 0.25 DEG C/min DEG C, keeps 75 minutes;
The cooling of described filter screen spray silk oils half elastic force stretch processing: by multistage for described melt straight melt-spun silk via the homogeneous fused mass after twin (double) screw extruder, enter back taper fondant filter, built-in three the parallel filter nets of described back taper fondant filter, described three parallel filter nets from top to bottom mesh diminish successively, spinning pump accurate measurement is delivered to by melt distributing pipe after filtration, the nascent strand of ejection in the special-shaped composite component be incubated by spinning manifold is accordingly evenly distributed to by multiple isometric S shape melt pipe, cooling forming is carried out successively again through ring blowing device, oil nozzle oils, then drawing and heat-setting is carried out, then described nascent strand is more successively after multiple tracks tension rollers and multiple pre-Network device, again after the control roll that three road tension force successively decrease successively, enter the draw zone being provided with three groups of drawing-off hot-rollings again and carry out share split drawing-off, again after six groups of sizing hot-rolling share split HEAT SETTING of symmetry, plying enters master network device and carries out network processes, then coiling and molding is carried out via up-coiler.
CN201310299679.4A 2013-07-17 2013-07-17 Terylene has the manufacture craft of light abnormity half elastic force drafting Active CN104294397B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310299679.4A CN104294397B (en) 2013-07-17 2013-07-17 Terylene has the manufacture craft of light abnormity half elastic force drafting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310299679.4A CN104294397B (en) 2013-07-17 2013-07-17 Terylene has the manufacture craft of light abnormity half elastic force drafting

Publications (2)

Publication Number Publication Date
CN104294397A CN104294397A (en) 2015-01-21
CN104294397B true CN104294397B (en) 2016-04-20

Family

ID=52314338

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310299679.4A Active CN104294397B (en) 2013-07-17 2013-07-17 Terylene has the manufacture craft of light abnormity half elastic force drafting

Country Status (1)

Country Link
CN (1) CN104294397B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105177732A (en) * 2015-10-21 2015-12-23 东华大学 Method for filtering and deaerating high-viscosity spinning solution during melt direct spinning

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1403635A (en) * 2001-09-13 2003-03-19 中国石化上海石油化工股份有限公司 Production process of composite Dacron filament with different fiber and different shrinkage
CN102586906A (en) * 2012-02-09 2012-07-18 桐乡市中辰化纤有限公司 Production method of circular-blow multi-end bright profiled polyester filament yarns more than 3dpf (denier per filament)
CN102586939A (en) * 2012-03-06 2012-07-18 江苏天地化纤有限公司 Profiled fire-retardant bright terylene FDY (Fully Drawn Yarn) filament and production process thereof
CN103526323A (en) * 2013-09-27 2014-01-22 苏州大学 Copolyester melt direct-spinning controllable multiple differential shrinkage composite fiber and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1403635A (en) * 2001-09-13 2003-03-19 中国石化上海石油化工股份有限公司 Production process of composite Dacron filament with different fiber and different shrinkage
CN102586906A (en) * 2012-02-09 2012-07-18 桐乡市中辰化纤有限公司 Production method of circular-blow multi-end bright profiled polyester filament yarns more than 3dpf (denier per filament)
CN102586939A (en) * 2012-03-06 2012-07-18 江苏天地化纤有限公司 Profiled fire-retardant bright terylene FDY (Fully Drawn Yarn) filament and production process thereof
CN103526323A (en) * 2013-09-27 2014-01-22 苏州大学 Copolyester melt direct-spinning controllable multiple differential shrinkage composite fiber and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
三叶异形丝有光涤纶拉伸丝的试制;栾宏志等;《上海纺织科技》;20001031;第28卷(第05期);第10-11页 *

Also Published As

Publication number Publication date
CN104294397A (en) 2015-01-21

Similar Documents

Publication Publication Date Title
CN103526323B (en) Copolyester melt direct-spinning controllable multiple differential shrinkage composite fiber and preparation method thereof
CN107502974A (en) A kind of method that covering yarn of chopped fiber bag micropore alkali soluble polyester long filament prepares hollow woven product
CN102864507B (en) Preparation method and product of melt direct spinning superfine porous differential polyester fiber
CN103290507A (en) Preparation method of polymerized micro-amount modified super bright polyester fibers
CN102677239A (en) Environment-friendly heather grey effect composite deformation filament yarn production process
CN106400175A (en) Production method of pre-spinning colored high-shrinkage polyester FDYs (Fully Drawn Yarns)
CN104294393B (en) Fused mass directly spinning high color fastness injects the processing technology of High Modulus And Low Shrinkage polyester filament in real time
CN102828278A (en) Polyester fully-drawn slub yarn and preparation method thereof
CN102330188A (en) Method for preparing nano silicon dioxide modified polyester fibers
CN102330172A (en) Nano titanium dioxide-modified terylene pre-oriented yarn
CN103484968A (en) Pre-oriented yarn made from copolyester melt through direct spinning, and preparation method of pre-oriented yarn
CN103590140B (en) A kind of imitative multiple polyisocyanate of linen look is combined short fibre and manufacture method thereof
CN102787383A (en) 1,2-propylene glycol modified terylene fully drawn yarn
CN102330184A (en) Modified terylene fully drawn yarn (FDY) with good abrasion resistance performance
CN104294397B (en) Terylene has the manufacture craft of light abnormity half elastic force drafting
CN104562250A (en) Micro-porous fine denier nylon 6 three-difference fiber and preparation method and application thereof
CN102330178A (en) Modified polyester fully drawn yarn with antibacterial effect
CN102719908A (en) Direct-spun black yarn FDY processing process based on master batch injection melt
CN102443861A (en) Intermediate-strength coarse-denier dacron FDY (Fully drawn yarn) and method for producing same
CN102330181A (en) Nanometer zinc oxide modified terylene low-elasticity network yarn
CN102330189A (en) Preparation method of nano-tin dioxide modified polyester fiber
CN104294394B (en) The processing technology of the pre-network long filament of POY bicomponent filament yarn multiple tracks
CN102330186A (en) Nano silver oxide modified polyester low-elasticity network yarns
CN102787388A (en) Nano-titanium dioxide modified terylene low elastic interlaced yarn
CN104153029A (en) Ultrafine polyamide 6 filament

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant