CN1693543A - Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre - Google Patents

Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre Download PDF

Info

Publication number
CN1693543A
CN1693543A CN 200510025708 CN200510025708A CN1693543A CN 1693543 A CN1693543 A CN 1693543A CN 200510025708 CN200510025708 CN 200510025708 CN 200510025708 A CN200510025708 A CN 200510025708A CN 1693543 A CN1693543 A CN 1693543A
Authority
CN
China
Prior art keywords
screw extruder
ppta
double screw
mixing
continuously
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.)
Granted
Application number
CN 200510025708
Other languages
Chinese (zh)
Other versions
CN100395381C (en
Inventor
刘兆峰
尤秀兰
陈蕾
潘婉莲
胡祖明
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.)
Donghua University
Original Assignee
Donghua University
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 Donghua University filed Critical Donghua University
Priority to CNB2005100257083A priority Critical patent/CN100395381C/en
Publication of CN1693543A publication Critical patent/CN1693543A/en
Application granted granted Critical
Publication of CN100395381C publication Critical patent/CN100395381C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Artificial Filaments (AREA)

Abstract

The invention discloses a method for continuously preparing p-phenylene terephthalamide (PPTA) fiber, including the steps of: (1) continuously adding 98-100% oil of vitriol and PPTA with specific logarithmic viscosity of 4.0-8.5 dl/g to an double spiral extruder, where the weight percent of PPTA is 14-24% and the mixing temperature is 50-100 deg.C; (2) fully mixing and entering in the other extruder, where the adjusting temperature is 50-100 deg.C and the staying time is 10-60 min, fully mixing, adjusting temperature and defoaming and then extruding them; (3) after measuring and filtering spinning solution, obtaining the invention by the routine steps, such as dry spraying-wet spinning. The advantages are short time for mixing materials, adjusting temperature and defoaming high mixing uniformity of materials able to implement continuous, stable filature in a short time, raising the production efficiency.

Description

A kind of method of continuously preparing poly poly P phenylene diamine terephthalamide fiber
Technical field
The present invention designs a kind of fiber preparation method, particularly relates to a kind of method of continuously preparing poly poly P phenylene diamine terephthalamide fiber
Background technology
As everyone knows, the Fanglun 1414 is a kind of typical aromatic polyamide fibre, be called Fanglun l414 or PPTA fiber again, it has high-strength, Gao Mo, excellent properties such as high temperature resistant, it is a class tec fiber with the fastest developing speed in the fibrous material in recent years, mainly use on fabrics for industrial use, particularly many product requirement lightweights, high performance occasion can only be used PPTA (PPTA) fiber.
Last century, early seventies was that PPTA/H has at first invented in E.I.Du Pont Company by U.S.A 2SO 4Liquid crystal solution is done the method for spray-wet spinning, has made the PPTA fiber of this high-strength and high-modulus, but still exists PPTA/H so far 2SO 4The stirring of the preparation process medium-high viscosity solution of spinning liquid crystal solution and deaeration difficult technologies problem, generally, the PPTA resin dissolves under 80~90 ℃ of conditions in 99~100% sulfuric acid, needs 3 hours at least, and PPTA/H 2SO 4The deaeration of spinning liquid crystal solution often needs the longer time, reaches tens hours to tens hours, and not only bad for the industrial production of serialization, and PPTA degrading in dissolving and the deaeration process for a long time easily, thereby influences the intensity of PPTA fiber.
A kind of semicontinuous Fanglun 1414's of preparation method is disclosed in the Chinese invention patent 200310109240, after mixing in PPTA resin and the concentrated sulfuric acid adding mixing drum, carry out double screw extruder, solve the problem of the long and spinning solution deaeration difficulty of the dissolution time of PPTA resin in the concentrated sulfuric acid, but for industrialization is produced, also had the problem that stirs difficulty and be difficult for mixing in the mixed process.
Summary of the invention
Technical problem to be solved by this invention is: a kind of method of continuously preparing poly poly P phenylene diamine terephthalamide fiber is provided, to remedy the deficiencies in the prior art and defective, meets the needs of production.
In order to solve the problems of the technologies described above the technical solution adopted in the present invention be: a kind of method of continuously preparing poly poly P phenylene diamine terephthalamide fiber may further comprise the steps:
(1) be 98~100% the concentrated sulfuric acid with concentration and dry logarithmic viscosity number is that the PPTA resin of 4.0~8.5dl/g adds double screw extruder 1 continuously, wherein the percentage by weight of PPTA resin is 14~24%, mixing temperature is 50~100 ℃, the time of staying is 1~10 minute, and the shear rate of double screw extruder 1 is 300~2000s -1
(2) above material enters double screw extruder 2 continuously after fully mixing, and regulating temperature is 50~100 ℃, and the time of staying is 10~60 minutes, extruding spinning solution after fully mixing, temperature adjustment, the deaeration;
(3) after spinning solution metering, the filtration, obtain poly-paraphenylene terephthalamide's diphenylamines fiber through doing conventional steps such as spray-wet spinning.
As optimized technical scheme: the concentrated sulfuric acid adopts liquid meter charging system weighing, and the PPTA resin adopts the metering of high accuracy weight-loss type continuous metering electronic scale.
The screw diameter of described double screw extruder 1 is 25~90mm, and draw ratio is 8~20, can be in the same way, also incorgruous rotation, and rotating speed is 150~300rpm.
The screw diameter of described double screw extruder 2 is 25~145mm, and draw ratio is 30~60, and screw speed is 10~200rpm, and the time of staying of material in this screw extruder is 10~60 minutes.
Two screw rods of described double screw extruder 1 are made up of to the deep trouth threaded block multistage bull or single head just (or anti-), on the forward screw thread, also have the reverse shallow thread groove of bull, therefore material has strong back mixing effect therein, and automatic cleaning action is good and shear rate is high, can reach 300~2000s -1, material can reach microcosmic at short notice to be mixed, thereby can improve PPTA and H 2SO 4Mixing uniformity.
The first half of two intermeshing screw rods in the described double screw extruder 2, from the screw rod total length that enters the mouth 30~80% part, kneading piece and a spot of reverse thread cover by various forward thread bush, different rotation directions are formed, wherein, the total length of kneading piece accounts for more than 30% of this partial-length.
The latter half of two intermeshing screw rods is made up of the thread bush that reduces gradually along Way out pitch in the described double screw extruder 2.
The invention has the beneficial effects as follows: mixing of materials, temperature adjustment, deaeration time weak point, the mixture homogeneity height of material can be realized continuous, stable spinning in the short time, has improved production efficiency.
The specific embodiment
Below in conjunction with specific embodiment the present invention is further elaborated.
Embodiment 1
Adopting liquid meter charging system and high accuracy weight-loss type continuous metering electronic scale that 100% concentrated sulfuric acid and PPTA (PPTA) powder are added diameter with the speed of 71.08g/min and 16.6g/min respectively is Φ 40, draw ratio is 15, incorgruous rotation, rotating speed is in the double screw extruder 1 of 200rpm, after fully mixing, entering diameter continuously is 55mm, draw ratio is 60, rotating speed is in the double screw extruder 2 of 40rpm, control double screw extruder 1,2 extruder temperature is 85 ℃, extrude abundant mixing continuously, adjustment is good, bubble takes off most spinning solution, through metering, after the filtration, send into spinning head, the spinneret cap specification is Φ 0.06 * 300 hole, through the air gap of 5cm layer, enter the coagulating bath spin duct, coagulation bath temperature is 5 ℃, and spinning speed is 120m/min, 6 times of jet stretches, spun tow is after the washing neutralization, send into annealing device, 400 ℃ of 10 seconds of following heat treatment, reoiling is wound into tube, measure according to GB, the intensity of gained PPTA (PPTA) fiber is 2.71GPa, and initial modulus is 182GPa, and extension at break is 1.41%.
Embodiment 2
Adopting liquid meter charging system and high accuracy weight-loss type continuous metering electronic scale that 99% concentrated sulfuric acid and PPTA (PPTA) powder are added diameter with the speed of 71.08g/min and 16.6g/min respectively is Φ 25, draw ratio is 8, rotation in the same way, rotating speed is in the double screw extruder 1 of 150rpm, after fully mixing, entering diameter continuously is 25mm, draw ratio is 30, rotating speed is in the double screw extruder 2 of 200rpm, control double screw extruder 1,2 extruder temperature is 50 ℃, extrude abundant mixing continuously, adjustment is good, bubble takes off most spinning solution, through metering, after the filtration, send into spinning head, the spinneret cap specification is Φ 0.06 * 300 hole, through the air gap of 5cm layer, enter the coagulating bath spin duct, coagulation bath temperature is 5 ℃, and spinning speed is 120m/min, 6 times of jet stretches, spun tow is after the washing neutralization, send into annealing device, 400 ℃ of 10 seconds of following heat treatment, reoiling is wound into tube, measure according to GB, the intensity of gained PPTA (PPTA) fiber is 2.75GPa, and initial modulus is 185GPa, and extension at break is 1.41%.
Embodiment 3
Adopting liquid meter charging system and high accuracy weight-loss type continuous metering electronic scale that 98% concentrated sulfuric acid and PPTA (PPTA) powder are added diameter with the speed of 70.08g/min and 20.6g/min respectively is Φ 90, draw ratio is 20, incorgruous rotation, rotating speed is in the double screw extruder 1 of 300rpm, after fully mixing, entering diameter continuously is 145mm, draw ratio is 60, rotating speed is in the double screw extruder 2 of 10rpm, control double screw extruder 1,2 extruder temperature is 100 ℃, extrude abundant mixing continuously, adjustment is good, bubble takes off most spinning solution, through metering, after the filtration, send into spinning head, the spinneret cap specification is Φ 0.06 * 300 hole, through the air gap of 5cm layer, enter the coagulating bath spin duct, coagulation bath temperature is 5 ℃, and spinning speed is 120m/min, 6 times of jet stretches, spun tow is after the washing neutralization, send into annealing device, 400 ℃ of 10 seconds of following heat treatment, reoiling is wound into tube, measure according to GB, the intensity of gained PPTA (PPTA) fiber is 2.73GPa, and initial modulus is 183GPa, and extension at break is 1.31%.
The comparative result that conventional spinning method, semicontinuous spinning process (200310109240) and the inventive method is spinned the 2Kg Fanglun 1414 respectively is as shown in table 1.
Table 1 with traditional spinning, semicontinuous spinning process and the inventive method relatively
Sample Intensity (GPa) Modulus (GPa) Mixing, dissolving, spinning time
Conventional spinning method ??2.62 ??181 12.5 hour
Semicontinuous spinning process ??2.60 ??180 4 hours
The embodiment of the invention 1 ??2.71 ??182 2 hours

Claims (5)

1, a kind of method of continuously preparing poly poly P phenylene diamine terephthalamide fiber is characterized in that, may further comprise the steps:
(1) be 98~100% the concentrated sulfuric acid with concentration and dry logarithmic viscosity number is that the PPTA resin of 4.0~8.5dl/g adds double screw extruder (1) continuously, wherein the percentage by weight of PPTA resin is 14~24%, mixing temperature is 50~100 ℃, the time of staying is 1~10 minute, and the shear rate of double screw extruder (1) is 300~2000s -1
(2) above material enters double screw extruder (2) continuously after fully mixing, and regulating temperature is 50~100 ℃, and the time of staying is 10~60 minutes, extruding spinning solution after fully mixing, temperature adjustment, the deaeration;
(3) after spinning solution metering, the filtration, obtain poly-paraphenylene terephthalamide's diphenylamines fiber through doing conventional steps such as spray-wet spinning.
2, preparation method according to claim 1 is characterized in that: the concentrated sulfuric acid adopts liquid meter charging system weighing, and the PPTA resin adopts the metering of high accuracy weight-loss type continuous metering electronic scale.
3, preparation method according to claim 1 is characterized in that: the screw diameter of described double screw extruder (1) is 25~90mm, and draw ratio is 8~20, and in the same way or incorgruous rotation, rotating speed is 150~300rpm.
4, preparation method according to claim 1 is characterized in that: two screw rods of described double screw extruder (1) are made up of to the deep trouth threaded block multistage bull or single head just (or anti-), also have the reverse shallow thread groove of bull on the forward screw thread.
5, preparation method according to claim 1, it is characterized in that: the screw diameter of described double screw extruder (2) is 25~145mm, draw ratio is 30~60, screw speed is 10~200rpm, the time of staying of material in this screw extruder is 10~60 minutes, the first half of two intermeshing screw rods, from the screw rod total length that enters the mouth 30~80% part, be by various forward thread bush, the kneading piece of different rotation directions, and a spot of reverse thread cover is formed, wherein, the total length of mediating piece accounts for more than 30% of this partial-length, the latter half of two intermeshing screw rods is made up of the thread bush that reduces gradually along Way out pitch.
CNB2005100257083A 2005-05-10 2005-05-10 Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre Expired - Fee Related CN100395381C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100257083A CN100395381C (en) 2005-05-10 2005-05-10 Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100257083A CN100395381C (en) 2005-05-10 2005-05-10 Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre

Publications (2)

Publication Number Publication Date
CN1693543A true CN1693543A (en) 2005-11-09
CN100395381C CN100395381C (en) 2008-06-18

Family

ID=35352659

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100257083A Expired - Fee Related CN100395381C (en) 2005-05-10 2005-05-10 Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre

Country Status (1)

Country Link
CN (1) CN100395381C (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101871129A (en) * 2009-04-27 2010-10-27 盐城市兰邦工业纤维有限公司 Preparation method of alkali-soluble hydroxyethylcellulose fiber spinning solution with high solid content
CN101555631B (en) * 2008-04-10 2011-04-06 中国神马集团有限责任公司 Industrial method for preparing PPTA spinning slurry with solid sulphuric acid
CN101220530B (en) * 2007-01-08 2011-06-22 上海艾麦达化纤科技有限公司 Production of uniform polyphenylene terephthalamide fibre
CN102268743A (en) * 2011-05-06 2011-12-07 上海舟汉纤维材料科技有限公司 Device and method for efficiently dissolving poly(p-phenytene terephthalamide) resin
CN102471933A (en) * 2009-08-11 2012-05-23 利斯特股份公司 Method for treating monomer, pre-polymer, polymer or corresponding mixture
CN102953128A (en) * 2012-04-16 2013-03-06 国能飞腾科技有限公司 Continuous spinning system of poly (p-phenylene terephthalamide)
CN105696104A (en) * 2016-04-21 2016-06-22 山东万圣博科技股份有限公司 Method for preparing black para-aramid fibers
CN109295506A (en) * 2018-09-13 2019-02-01 清华大学 A kind of p-aramid fiber spinning solution compounding system and its preparation method

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL172680C (en) * 1979-06-08 1983-10-03 Akzo Nv PROCESS FOR MANUFACTURING FIBERS FROM POLY-P-PHENYLENE DEPTHALAMIDE AND THE PRODUCTS PRODUCED SO.
US5582911A (en) * 1990-12-27 1996-12-10 Michelin Recherche Et. Technique, S.A. Aramid monofilament having a slightly structured skin--process for producing this monofilament
NL1000276C2 (en) * 1995-05-02 1996-11-05 Akzo Nobel Nv Process for the production of fibers from poly (p-phenylene terephthalamide).
CN1047414C (en) * 1995-06-07 1999-12-15 刘兆峰 Ultrastrength polyethylene fibre spinning apparatus
CN1187393C (en) * 2002-08-12 2005-02-02 东华大学 preparation method of para Fanglun slurry cake
CN1256474C (en) * 2003-12-10 2006-05-17 中国石化仪征化纤股份有限公司 Manufacturing method of poly p phenylene diamine terephthalamide fiber

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101220530B (en) * 2007-01-08 2011-06-22 上海艾麦达化纤科技有限公司 Production of uniform polyphenylene terephthalamide fibre
CN101555631B (en) * 2008-04-10 2011-04-06 中国神马集团有限责任公司 Industrial method for preparing PPTA spinning slurry with solid sulphuric acid
CN101871129A (en) * 2009-04-27 2010-10-27 盐城市兰邦工业纤维有限公司 Preparation method of alkali-soluble hydroxyethylcellulose fiber spinning solution with high solid content
CN102471933A (en) * 2009-08-11 2012-05-23 利斯特股份公司 Method for treating monomer, pre-polymer, polymer or corresponding mixture
CN102268743A (en) * 2011-05-06 2011-12-07 上海舟汉纤维材料科技有限公司 Device and method for efficiently dissolving poly(p-phenytene terephthalamide) resin
CN102268743B (en) * 2011-05-06 2013-04-03 上海舟汉纤维材料科技有限公司 Device and method for efficiently dissolving poly(p-phenytene terephthalamide) resin
CN102953128A (en) * 2012-04-16 2013-03-06 国能飞腾科技有限公司 Continuous spinning system of poly (p-phenylene terephthalamide)
CN105696104A (en) * 2016-04-21 2016-06-22 山东万圣博科技股份有限公司 Method for preparing black para-aramid fibers
CN109295506A (en) * 2018-09-13 2019-02-01 清华大学 A kind of p-aramid fiber spinning solution compounding system and its preparation method
CN109295506B (en) * 2018-09-13 2020-07-28 清华大学 Para-aramid spinning solution preparation system and preparation method thereof

Also Published As

Publication number Publication date
CN100395381C (en) 2008-06-18

Similar Documents

Publication Publication Date Title
CN1693543A (en) Method of continuously preparing poly terephthaloyl-p-phenylene diamine fibre
RU2625306C2 (en) Method of manufacture of lignin-containing prediminary fiber, and also of carbon fibers
CN1298900C (en) Cellulose multi-filament for tyre cord and its producing method
CN106012103B (en) A kind of preparation method of high intensity alginate fibre
CN1247835C (en) Apparatus and method for spinning hollow polymeric fibres
JP2005515309A (en) Polypeptide fibers and methods for their production
CN101994161A (en) Method for preparing polytetrafluoroethylene superfine fiber
CN100427650C (en) High shearing rate method for spinning poly-terephthaloyl p-phenylenediamine fibre
CN1256474C (en) Manufacturing method of poly p phenylene diamine terephthalamide fiber
KR20140002991A (en) Process for manufacturing cellulose-based carbone fibers
CN112941657B (en) Spinning forming method of poly (p-phenylene-benzobisoxazole) fibers
CN101736411A (en) Method for preparing polyacrylonitrile spinning solution for carbon fiber
CN115787124A (en) Preparation process of superfine denier para-aramid fiber
CN101220530B (en) Production of uniform polyphenylene terephthalamide fibre
CN201092591Y (en) Continuous defoaming device for manufacturing homogeneous Poly(p-phenyleneterephthalamide) fibre
CN1232686C (en) Polyimide fibre and its preparing process
CN1079121C (en) Preparation of spinnable isotropic cellulose solution
CN104278338A (en) Gel spinning method for manufacturing aramid fiber III
CN101608347A (en) A kind of gradient coagulating bath device for preparing polyphenylene Ben Bing Er oxazole fiber
CN101906677B (en) Preparation method of anti-ultraviolet aging polyphenylene benzodioxazole fiber
JP2001316936A (en) Method for producing solvent spun cellulose fiber
CN113373540B (en) Polyacrylonitrile fiber and preparation method thereof
CN217869236U (en) Horizontal multistage water washing device for preparing polyacrylonitrile-based carbon fiber precursor
CN106192041B (en) A kind of preparation method of cellulose fibre
Alfonso et al. Ultrahigh‐modulus fibers from rigid and semirigid aromatic polyamides

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
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20080618

Termination date: 20170510

CF01 Termination of patent right due to non-payment of annual fee