CN1077760A - Polyamide-imides wiredrawing method and prepared fiber - Google Patents
Polyamide-imides wiredrawing method and prepared fiber Download PDFInfo
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- CN1077760A CN1077760A CN92113840A CN92113840A CN1077760A CN 1077760 A CN1077760 A CN 1077760A CN 92113840 A CN92113840 A CN 92113840A CN 92113840 A CN92113840 A CN 92113840A CN 1077760 A CN1077760 A CN 1077760A
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/74—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polycondensates of cyclic compounds, e.g. polyimides, polybenzimidazoles
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
Abstract
The present invention relates to prepare the method for PAI fiber and prepared fiber thereof by the wire drawing of PAI solution.
Dry method or wet wire drawing in dimethyl alkylidene urea, again remove desolvate, and at high temperature excessive drawing and obtain fiber.
Prepared silk and fiber by with toluylene group diisocyanate or metaphenylene vulcabond be main component PAI and aromatics acidity acid anhydrides and/or aromatic dianhydride, also have one or more diacid compounds and obtain.
They have good thermo mechanical stability, and the fibre number that can reach is very low.
Description
The present invention relates to obtain the method for thermally-stabilised fiber and the fiber that obtains thus by the wire drawing of polyamide-imides solution.
Know by FR2079785, in the aqueous fluid that also contains N-methyl-pyrrolidones, N-methyl-pyrrolidone polymer solution wet method is reeled off raw silk from cocoons, draws then, washed, drying is produced with the polyamide-imides is the Fil-Lumiere of key component, contain from 3 of alkali metal or alkaline-earth metal at least 3% crosslinking agent of 5-dicarboxyl benzene sulfonate in the described key component.
But this silk is except color is buff, and concerning some was used, its thermo mechanical stability not enough.
In addition, according to this patent, when utilizing toluylene and metaphenylene vulcabond as initial vulcabond, the polyamide-imides fiber that can not obtain having good mechanical properties.
In order to improve the engineering properties of polyamide-imides, according to FR2643084 also prepared by 4,4 '-polyamide-imides that the diphenyl ether vulcabond obtains is the fiber of key component.But the tensility of this fibrid is low, can not reach low fibre number.
In addition, 4,4 '-the diphenyl ether vulcabond is to be difficult on a kind of market buy and very expensive product.
The present invention relates to a kind of producing with the polyamide-imides is the silk of main component and the method for fiber, and itself and fiber are to be obtained by the polymer solution drawing that comprises following part in dimethyl alkylidene urea:
-have an amide-imide chain (A) of following chemical formula:
-may have the acid amides chain (B) of following chemical formula:
-may have the acid amides chain (C) of following chemical formula:
-have an acid imide chain (D) of following chemical formula:
In the formula:
*Ar
1Represent toluylene and/or metaphenylene divalent aryl,
*Ar
2Represent the trivalent aryl,
*Ar
3Represent the tetravalence aryl,
*R represents divalent aryl
*M represents alkali metal or alkaline-earth metal
Chain (A) is 0-100%, 20-100% preferably,
Chain (B) is 0-5%,
Chain (C) is 0 to＜100%, 0-80% preferably,
Chain (D) is 0 to＜100%, 0-80% preferably,
Chain (A)+(B)+(C)+(D) and equal 100%,
Moisture setting medium contains 30-80%(weight) dimethyl alkylidene urea (DMAU), preferably 50-65%(weight)
-draw resulting silk with at least 2 * ratio,
-remove residual solvent
-with known method drying,
-with the excessive drawing of at least 2 * ratio, best at least 3 * ratio, temperature is at least 250 ℃, usually at least 300 ℃ or even higher, always draw ratio and be at least 5 *, preferably at least 6 *.
Best, the inherent viscosity 〉=0.8dl/g of the polyamide-imides of use.The dimethyl alkylidene urea that uses is dimethyl ethylidene-urea or dimethylpropylene urea preferably.
Silk of the present invention and fiber can also be in dimethyl alkylidene ureas, are 15-35% by containing above-mentioned chemical formula copolymer chain A, B, C, the polyamide-imides of D, concentration, and preferably the solution dry method of 20-30% draws and prepares the Ar among A, B, C, the D
1, Ar
2, Ar
3, R and M have same implication, its temperature remains on the boiling point that is close to or higher than solvent in evaporation atmosphere, wants its residual solvent of flush away at the silk of container for evaporation outlet., can wash with water for this reason, perhaps can under pressure, wash with boiled water, with method drying commonly used, be preferably in be higher than under 80 ℃ of temperature dry.Can also be under reduced pressure and/or ℃ heat-treat in temperature 〉=160 in the inert atmosphere; After the eccysis residual solvent, be higher than under 250 ℃ of temperature, be preferably in and be higher than under 300 ℃ of temperature, preferably also draw under the situation of oxygen not having.
Total drawing rate of being implemented is 5 at least *, preferably be 6 at least *.
This base polymer can be obtained by reaction (a), obviously with the ratio of stoichiometric amount with do not have under the situation of catalyst, in polar solvent, be selected from 2,4-toluylene or 2,6-toluylene group diisocyanate, or at least a aromatics two isocyanic acid acid anhydrides in the metaphenylene vulcabond, with at least a acid reactant reaction, its acid reactant contains a kind of aromatic anhydride-acid, perhaps a kind of aromatic dianhydride, perhaps 3 of a kind of alkali metal or alkaline-earth metal, 5-dicarboxyl benzene sulfonate, perhaps a kind of aromatic diacid, its operating condition are described in the french patent application 1600067 that proposes December 30 nineteen sixty-eight.
These polymer can also be made by reaction (b), do not having in the presence of the aromatic anhydride, during in stoichiometric amount ratio and catalyst-free, aforesaid one or more vulcabond and a kind of acid reactant reaction (b), its acid reactant comprises a kind of aromatic dianhydride, aromatic diacid, perhaps with 3 of a kind of alkali metal or alkaline-earth metal, 5-dicarboxylic acids benzene sulfonate reacts (b).
When utilizing reaction (a), the ratio of its different chains is as follows:
-chain (A): 20-100%
-chain (B): 0-5%
-chain (C): 0-80%
-chain (D): 0-80%
When utilizing reaction (b), the ratio of its chain is as follows:
-chain (A): 0%
-chain (B): 0-5%
-chain (C): 0-＜100%, preferably 0-80%
-chain (D): 0-＜100%, preferably 0-80%
Chain (A)+(B)+(C)+(D) sum is 100%.
The used vulcabond of preparation polyamide-imides is 2.4-or 2.6-toluylene group diisocyanate, a diphenylene vulcabond or their mixture.The toluylene group diisocyanate is 2.4-and 2.6-toluylene based mixtures (TDI-2.4 and 2.6) on the market.Preferably this mixture is made up of 60%TDI-2.4 at least.
Perhaps, can add other aromatics aliphatic series or cycloaliphatic diisocyanates of low ratio in aforementioned vulcabond, its purpose is to improve some character of made goods; For example, may be significant by phenylene vulcabond (p-PDI) replacement m-PDI is up to the engineering properties improvement that obtained fiber at 30% o'clock.
The most handy trihemellitic acid acid anhydride is made acid anhydrides, as aromatic dianhydride, can quote pyromellitic acid dicarboxylic anhydride, diphenyl 3,3 ', 4,4 ' tetrabasic carboxylic acid dicarboxylic anhydride, naphthalene-2,3,6,7 tetrabasic carboxylic acid dicarboxylic anhydrides, diphenyl ether-3,3 ', 4,4 ' tetrabasic carboxylic acid dicarboxylic anhydride, diphenyl sulfone-3,3 ', 4,4 ' tetrabasic carboxylic acid dicarboxylic anhydride, preferably diphenylketone-3,3 ', 4,4 ' tetrabasic carboxylic acid dicarboxylic anhydride.Can mix use by a plurality of acid anhydrides in these acid anhydrides; In aromatic diacid, often use benzene two (first) acid and a benzene two (first) acid, though some other dicarboxylic acids such as diphenyldicarboxylic acid or naphthalene dicarboxylic acids also can suit to benzene two (first) acid is more welcome.The trihemellitic acid acid anhydride that uses should be pure, especially can not contain the mole above 5%() trihemellitic acid.
3 of alkali metal or alkaline-earth metal, 5-dicarboxyl benzene sulfonate is sodium sulfonate or potassium sulfonate preferably.
Different acid or acid anhydrides-acid and anhydride compounds have following mol ratio:
Aromatic anhydride-acid: be in a ratio of 0-100% with the acid reactant total amount, 20-100% preferably,
Aromatic diacid: 0-＜100%, 0-80% preferably,
Dicarboxyl benzene sulfonate ratio is 0-5%
Aromatic dianhydride: be in a ratio of 0-＜100% with the acid reactant total amount, the characteristic of the polymer that obtains like this (intrinsic) viscosity is at least 0.8dl/g, best 0.9dl/g at least, so that can reel off raw silk from cocoons, the silk that obtains has favorable mechanical character.
When being lower than these viscosity numbers, this is corresponding to the molecular weight deficiency, and the silk that obtains is difficult to use.
Polyamide-imides also has glass transition temperature and is at least 290 ℃, generally is higher than 300 ℃, and this helps silk to reach good thermo mechanical stability.Inherent viscosity is illustrated in 0.8 millimeter capillary of diameter, 0.5%(weight/volume in 25%DMEU) length of polymer solution flow time.
η＝4.6（log tl-log to）
To(is in second) be the flowing time of neat solvent
Tl(is in second) be the flow of solution time
In the organic polar solvent that uses, use dimethyl alkylidene urea, as dimethyl ethylidene-urea or dimethylpropylene urea, the polyamide-imides solution that reel off raw silk from cocoons has not too the advantage with look.These solution also have the viscosity that can reel off raw silk from cocoons, be generally the 400-1000 pool, preferably 500-800 pool is used for wet method and reels off raw silk from cocoons, and the 1500-3000 pool is used for dry method and reels off raw silk from cocoons, and viscosity is to be that the known-viscosity instrumentation of EPPRECHT RHEOMAT 15 is fixed with the market ATTACH LABEL.
Polymerisation in solution substrate concentration to be reeled off raw silk from cocoons can be 10-35%, preferably 15-25%.Its solution can contain and is useful on the FINAL APPEARANCE of improving the gained silk or the various additives of character, as pigment, matifiants(admixture), stabilizing agent.
The temperature of solution of reeling off raw silk from cocoons can in very large range change according to the viscosity of the solution of waiting to reel off raw silk from cocoons.For example, low viscosity solution can be easy to push at normal temperatures, and high viscosity solution preferably heats, for example 120 ℃ or even higher temperature under push.Avoid in wire drawing die, using too big pressure like this.
Under the situation that wet method is reeled off raw silk from cocoons, the condensation water that the inventive method is used is a kind of 30-80%(of containing weight) aqueous solution of dimethyl alkylidene urea (DMAU), containing 50%(weight but be to use) condensation water of above DMAU usually is favourable, can better be drawn the silk of performance, therefore last performance also is preferably.
The speed in condensation water, passed through of silk can be along with its solvent strength and silk current distance in body lotion variation and in very large range change.For example, silk this passage rate in condensation water is easy to select between 10-60m/mn, still allows the speed that reaches higher.In view of the profitable reason of this method, generally be disadvantageous to reel off raw silk from cocoons than low velocity.In addition, in condensation water, the passage rate of silk is too high can to reduce the aerial drawability of silk.Considering economic benefit and selecting the passage rate of silk in condensation water when becoming yarn quality to require last.
For example, the temperature of condensation water can be selected between 15-40 ℃, and usually, this temperature is 20-30 ℃.
To draw the silk that obtains so so, preferably in air, with at least 2 * or higher ratio draw.
Be preferably in the air draw after, generally be between two groups of rollers, implement to draw after, at room temperature remove a last remaining solvent with known method, generally wash with the circulated in countercurrent water washing or washing on the roller.
The dry method silk that obtains that reels off raw silk from cocoons will be in the wire drawing chamber draws in advance, removes residual solvent then, perhaps being higher than heat treatment under 100 ℃ the temperature, perhaps washes with water, preferably washs with boiled water under pressure.
In two kinds of methods of reeling off raw silk from cocoons, the silk known method drying of having washed, for example dry in drier or on roller.Its baking temperature can in very large range change, and its temperature is high more, and its speed is then faster.Usually, to carry out drying be favourable to elevated temperature gradually, and this temperature can reach even above 200 ℃.
The silk of removing its solvent and water reaches good fibre number again through drawing to improve their mechanical quality for the second time, may be lower than 1dtex/brin, (d spy's (count system)/fiber).
Can carry out excessive control with all known means: stove, plate, roller, at least 250 ℃ of temperature, can preferably not have oxygen up to 400 ℃ by preferably at least 300 ℃.
Usually, excessive drawing is with at least 2 * ratio, preferably at least 3 * ratio is implemented, can reach 4 or 5 * so that always draw ratio and be at least 5 *, preferably at least 6 *.
According to the present invention, the PAI silk that is obtained by toluylene group diisocyanate or metaphenylene vulcabond has unexpected characteristics, has good drawability, can reach the fiber with excellent fiber number, be better than in FR2079785 and 2643084 describing such as 4,4 '-methyl diphenylene diisocyanate or 4,4 '-polyamide-imides that other vulcabond of diphenyl ether vulcabond and so on obtains.As narration in the back inquired for, it thread also has, and color is more shallow, thermo mechanical stability advantage preferably.
The invention still further relates to the polyamide-imides is the silk and the fiber of key component, and polyamide-imides is made up of following chain:
-have an amide-imide chain (A) of following chemical formula:
-perhaps have an acid amides chain (B) of following chemical formula:
-perhaps have an acid amides chain (C) of following chemical formula:
-have an acid imide chain (D) of following chemical formula:
In the formula:
*Ar
1Represent toluylene or metaphenylene aryl,
*Ar
2Represent the trivalent aryl
*Ar
3Represent the tetravalence aryl
*R represents divalent aryl
*M represents alkali metal or alkaline-earth metal
Chain (A) is 20-100%, 50-100% preferably,
Chain (B) is 0-5%,
Chain (C) is 0-＜100%, 0-50% preferably,
Chain (D) is 0 to＜100%, 20-100% preferably,
Chain A+B+C+D sum is 100%.
Itself and fiber have good thermo mechanical stability, and of light color.
Silk of the present invention and fiber preferably have inherent viscosity 〉=0.8dl/g, are preferably 0.9dl/g.
Be increased to about 400 ℃ by temperature gradually linearly by 0 ℃, and keep the elastic modelling quantity level to prove its thermo mechanical stability.The maintenance of elastic modelling quantity is to be 〉=40% at 310 ℃, be preferably 〉=50%.With the toluylene group diisocyanate is that its thermo mechanical stability of silk of making of the PAI of key component is high especially.What obtained by m-PDI is that the silk of key component has very shallow priming color with PDI, can make this series products with uncommon very light degree dyeing.
In addition, these silks be in 200 ℃ reach 1000 hours after, its toughness keeps at least 75%, preferably at least 80%, 200 ℃ reach 5000 hours after, its toughness keeps at least 65%, preferably at least 70%.
Silk of the present invention also has good drawability, can reach very low fibre number, and less than 1d spy/fiber (dtex/brin), for thermally-stabilised silk, this is very uncommon, and it is very soft to give fabric feeling.They also have the favorable mechanical performance, fracture toughness, elastic modelling quantity and low percentage elongation.They have textile touch, good mechanical properties and thermo-mechanical property simultaneously like this.They can be easy to use basic dyeing.
They can use separately, or mix use with natural silk or synthetic silk, and its purpose is to improve or improve some character, and they can find very wide range of application, and are especially all the more so aspect Work Clothes and protection clothes.
When silk does not have unit (B), it can also be joined in the composition of many composites, especially aspect dielectric applications.
At last, they also have very big economic benefit, because people know toluylene group diisocyanate and metaphenylene vulcabond and obtain easily, and the market price is not too high, this has very important industrial significance, with by 4,4 '-silk that the polyamide-imides of diphenyl ether vulcabond preparation obtains compares, this is significant especially.
In the following embodiments, Mn and Mw value rise number 80 ℃ of NMP neutralizations with 0.1 mole/lithium bromide with gel exclusion chromatography method (GPC) and measure, and its quality is to compare expression with polyphenyl alkene sample.
The polydispersity index I corresponding to
Ratio.
Embodiment 1-4(TDI):
Not having under the situation of catalyst, in the dimethyl ethylidene-urea, be 21% the copolyamide-imide solution that contains sulfo group by following compound prepared in reaction concentration:
244 milliliters of-DMEU 257.1 grams
0.5 mole of-toluylene group diisocyanate 87 gram
0.4 mole (80mol%) of-trihemellitic acid acid anhydride 76.8 grams
0.08 mole (16mol%) of-terephthalic acid (TPA) (AT) 13.28 grams
-3,0.02 mole (4mol%) of 5-dicarboxyl benzene sulfonic acid sodium salt 5.36 grams
250 milliliters of DMEU 263.7 grams of-dilution
Molecular weight Mn:50020
Polydispersity I: 1.78
Inherent viscosity: 0.97dl/g
The solution concentration that obtains is 21%, is 603 pools with its viscosity of EPPRECHT RHEOMAT 15 viscometer determinings.Groove D+E is 25 ℃.
Containing 62%(weight) DMEU and 38%(weight) in the DMEU/ water-setting solid-liquid of water, temperature is 27 ℃, with its temperature be 70 ℃ solution to be pressed through 62 holes, diameter be 0.06 millimeter drawing film, in its liquid, about 1 meter of the length that silk is advanced.Export at solidification liquid (bathroom), its silk is regained by the first row roller, and between first row and secondary series roller with ratio 2 * in air, draw water countercurrent washing in sink then, dry in the about 150 ℃ stove of maintenance, in the about 350 ℃ stove of maintenance, further draw again.
Implemented a plurality of excessive drawing rates.The characteristic of silk comes together in the following table I:
-heat endurance:
Place 200 ℃ to assign its toughness maintenance 80% after 1000 hours, assign maintenance 70% in 5000 hours at 200 ℃.
Form by the polyamide-imides that the above-mentioned same monomer except that toluylene obtains according to the silk that FR2643084 obtains, and the toluylene group diisocyanate is by 4,4 '-methyl diphenylene diisocyanate replaces, its silk 200 ℃ reach 1000 hours after toughness remain 38%.
-thermo mechanical stability: the maintenance of elastic modelling quantity and the relation of temperature:
-its fiber keeps 50% of its elastic modelling quantity in the time of 310 ℃.
-press FR2643084 preparation, with 4,4 '-methyl diphenylene diisocyanate is the fiber of main component, in the time of 310 ℃, only keeps 22.5% of its elastic modelling quantity.
Embodiment 5
Replace TDI by identical mol ratio by the metaphenylene vulcabond, prepare a kind of polyamide-imides in the mode that illustrates among the embodiment 1.
The molecular weight Mn of prepared PAI is 36560, and polydispersity index is 2.05, and inherent viscosity is 0.86dl/g.
The viscosity of measuring its solution with EPPRECHT RHEOMAT viscosimeter is 566 pools.
The polyamide-imides solution that makes like this is with 21% concentration wire drawing, and handles with the method for explanation among the embodiment 1, and with ratio 2.3 * carry out drawing in the air, also with ratio 2.3 * excessive drawing, drawing rate always is 5.29 *.
Resulting silk has following characteristic:
Long fiber fiber number (dtex): 2.3
Fracture toughness: 26g/tex
Fracture elongation: 18%
-in the toughness maintenance 75% after 1000 hours of 250 ℃ of heat ageings,
-thermo mechanical stability: keep 40% at 310 ℃ of elastic modelling quantity.
Embodiment 6-8: with the TDI KERMEL of 40%AT
In the dimethyl ethylidene-urea by the copolyamide-imide solution that contains sulfo group of following compound prepared in reaction concentration 21%:
238 milliliters of-DMEU 251.3 grams
0.5 mole of-toluylene group diisocyanate 87 gram
0.28 mole (56mol%) of-trihemellitic acid acid anhydride 53.76 grams
0.20 mole (40mol%) of-terephthalic acid (TPA) (AT) 33.20 grams
-3,0.02 mole (4mol%) of 5-dicarboxyl benzene sulfonic acid sodium salt 5.36 grams
244 milliliters of DMEU 257.40 grams of-dilution
Molecular weight M
n: 40560
Polydispersity I: 1.98
Inherent viscosity: 0.95dl/g
The solution that makes is 606 pools with its viscosity of EPPRECHT RHEOMAT 15 viscometer determinings.Groove D+E is 25 ℃.
Containing 62%(weight) DMEU and 38%(weight) in the DMEU/ water-setting solid-liquid of water, its liquid remains on 27 ℃, with temperature is that to be pressed through 62 holes, diameter be 0.06 millimeter wire drawing die for 70 ℃ solution, in this body lotion, about 1 meter of the length that silk is advanced, export at solidification liquid, its silk is regained by the first row roller, and between first row and secondary series roller with ratio 2 * in air, draw, water countercurrent washing in sink then, dry in keeping about 150 ℃ stove, excessive drawing in being maintained at about 350 ℃ stove then.
A plurality of excessive drawing rates have been implemented.Its characteristic comes together in the following table II:
Embodiment 9
Do not having under the situation of catalyst, in dimethylpropylene urea by following compound prepared in reaction concentration be 21% contain sulfo group copolyamide solution:
-dimethylpropylene urea (DMPU) 279.8 gram (d=1.064)=263.0ml
-trihemellitic acid acid anhydride 61.44 grams (0.32 mole)
-terephthalic acid (TPA) 13.28 grams (0.08 mole)
-phenylene-1,3-vulcabond 64 grams (0.4 mole)
103 milliliters of DMPU 109.6 grams of-dilution
Obtain a kind of in DMPU concentration be 21% solution, the viscosity of measuring by the method for explanation among the embodiment 1 is 810 pools.The molecular weight Mn=37840 of the PAI that makes like this, polydispersity is 2.34, inherent viscosity is 0.89dl/g.
Prepared solution is pressed among the embodiment method wire drawing of 1 explanation, and the silk that obtains is by drawing rate 2 * drawings, washing and drying, then in remaining in 335 ℃ stove with ratio 3 * excessive drawing.
Prepared silk has following characteristic
Long fiber fiber number (dtex) 2
Fracture toughness, 30g/tex
Percentage elongation, % 15
Thermo mechanical stability: remain 43% of initial modulus at 310 ℃ of elastic modelling quantity.
Embodiment 10-12:
Do not having under the situation of catalyst, in the dimethyl ethylidene-urea by a kind of concentration 21% sulfonation and copolymerization amide-imide solution of following compound prepared in reaction:
244 milliliters of-DMEU 257.1 grams
0.5 mole of-toluylene group diisocyanate 87 gram
0.4 mole (80mol%) of-trihemellitic acid acid anhydride 76.8 grams
0.08 mole (16mol%) of-terephthalic acid (TPA) (AT) 13.28 grams
-3,0.02 mole (4mol%) of 5-dicarboxyl benzene sulfonic acid sodium salt 5.36 grams
250 milliliters of DMEU 263.7 grams of-dilution
Molecular weight Mn:60100
Polydispersity I: 2
Inherent viscosity: 1dl/g
Obtain concentration and be 21% solution, the viscosity of measuring with EPPRECHT RHEOMAT 15 viscosimeters is 603 pools.Groove D+E is 25 ℃.In these embodiments, the DMEU of the polycondensation and the use of reeling off raw silk from cocoons especially circulates with the way of distillation after purifying in advance.
Containing 62%(weight) DMEU and 38%(weight) in the DMEU/ water-setting solid-liquid of water, its liquid remains on 28 ℃, temperature is remained on 70 ℃ solution, and to be pressed through 62 holes, diameter be 0.065 millimeter drawing film, about 1 meter of the length that silk is advanced in this body lotion.In solidification liquid outlet, its silk is regained by the first row roller, and between first row and secondary series roller with ratio 2.5 * in air, draw.Water countercurrent washing in sink then, dry in the about 120 ℃ stove of maintenance, excessive drawing in keeping the about 370 ℃ stove of temperature then.
A plurality of excessive drawing rates have been implemented.The characteristic of silk comes together in the following table III:
Thermo mechanical stability: the relation that keeps elastic modelling quantity and temperature:
At 310 ℃, fiber keeps 50% of its modulus.
-embodiment 13 and 14:
Not having under the situation of catalyst, in the dimethyl ethylidene-urea, by a kind of concentration 21% copolyamide of following compound prepared in reaction-imide solution:
0.5 mole of-toluylene group diisocyanate
0.4 mole of-trihemellitic acid acid anhydride (80mol%)
0.10 mole of-terephthalic acid (TPA) (AT) (20mol%)
-inherent viscosity 0.97dl/g
Containing 62%(weight) DMEU and 38%(weight) in the DMEU/ water-setting solid-liquid of water, its liquid remains on 28 ℃, temperature is remained on 70 ℃ solution, and to be pressed through 62 holes, diameter be 0.065 millimeter drawing film, about 1 meter of the length that silk is advanced in this body lotion.In solidification liquid outlet, its silk is regained by the first row roller, and between first row and secondary series roller with ratio 2.2 * in air, draw.Water countercurrent washing in sink then, dry in the about 120 ℃ stove of maintenance, excessive drawing in keeping the about 350 ℃ stove of temperature then.
Implemented multiple excessive drawing rate.The characteristic of silk comes together in the following table IV:
Degradation
Thermo mechanical stability: the relation that keeps elastic modelling quantity and temperature
-at 310 ℃, fiber keeps 50% of its modulus.
-embodiment 15-17
Not having under the situation of catalyst, in the dimethyl ethylidene-urea, by a kind of concentration 25% copolyamide of following compound prepared in reaction-imide solution:
-dimethyl ethylidene-urea (DMEU) 269.3 gram (d=1.056)=255 milliliter
-benzophenone tetracarboxylic anhydride 80.5 grams (0.25 mole) (50mol%)
-terephthalic acid (TPA) 41.5 grams (0.25 mole) (50mol%)
-toluylene group diisocyanate 87 grams (0.50 mole)
DMEU 185.7 grams (176 milliliters) of-dilution
Obtain a kind of in DMEU the solution of concentration 21%, the viscosity of measuring by the method that indicates among the embodiment 1 is 580 pools.The molecular weight Mn=36250 of the PAI that makes like this, polydispersity is 2.10.
Inherent viscosity is 0.85dl/g.
The solution that so makes is by the method wire drawing of explanation among the embodiment 1, and resulting silk is pressed and drawn ratio 2.2 * drawing, washs with dry excessive drawing in the stove of 345 ℃ of maintenances then.
Implemented multiple excessive drawing rate.The characteristic of silk comes together in the following table V:
Claims (19)
1, to have what improve thermo mechanical stability be the silk and the method for fiber of key component with the polyamide-imides in preparation, it is characterized in that:
A) in dimethyl alkylidene urea (DMAU), polymer solution wire drawing in moisture setting medium, polymer comprises:
-have an amide-imide chain (A) of following chemical formula:
-have an acid amides chain (B) of following chemical formula:
-have an acid amides chain (C) of following chemical formula:
-have an acid imide chain (D) of following chemical formula:
In the formula:
*Ar
1Represent toluylene and/or metaphenylene divalent aryl,
*Ar
2Represent the trivalent aryl,
*Ar
3Represent the tetravalence aryl,
*R represents divalent aryl
*M represents alkali metal or alkaline-earth metal
-chain (A) is 0-100%,
-chain (B) is 0-5%,
-chain (C) is 0 to＜100%,
-chain (D) is 0 to＜100%, is preferably 0-80%,
Chain (A)+(B)+(C)+(D) sum is 100%,
Moisture setting medium contains 30-80% (weight) dimethyl alkylidene urea (DMAU), and 20-70% (weight) water,
B) draw resulting silk with 2X ratio at least,
C) remove residual solvent on the silk, and with all known method dryings,
D) under at least 250 ℃ of temperature with its silk of the excessive drawing of 2X ratio at least, so that drawing rate always is at least 5X.
2,, it is characterized in that washing and remove its solvent by the described method of claim 1.
3, by the described method of claim 1, it is characterized in that condensation water contains 50-65%(weight) solvent.
4, by the described method of claim 1, it is characterized in that carrying out excessive drawing with at least 3 * ratio so that total draw (rate) be 6 *.
5, by the described method of claim 1, it is characterized in that under at least 300 ℃ of temperature not having to carry out excessive drawing under the situation of oxygen.
6, to have what improve thermo mechanical stability be the silk and the method for fiber of key component with the polyamide-imides in preparation, it is characterized in that: "
A) in dimethyl alkylidene urea (DMAU), contain the polymer solution wire drawing of following chain:
-have an amide-imide chain (A) of following chemical formula:
-have an acid amides chain (B) of following chemical formula:
-have an acid amides chain (C) of following chemical formula:
-have an acid imide chain (D) of following chemical formula:
In the formula:
*Ar
1Represent toluylene or metaphenylene divalent aryl,
*Ar
2Represent the trivalent aryl
*Ar
3Represent the tetravalence aryl
*R represents divalent aryl
*M represents alkali metal or alkaline-earth metal
Chain (A) is 20-100%,
Chain (B) is 0-5%,
Chain (C) is 0 to＜100%,
Chain (D) is 0 to＜100%, best 0-80%,
Chain (A)+(B)+(C)+(D) sum is 100%,
Wire drawing in being close to or higher than the evaporation atmosphere of solvent boiling point temperature is removed residual solvent from silk, draw being higher than under 250 ℃ of temperature then so that drawing rate always be at least 5 *.
7, by the described method of claim 6, it is characterized in that solvent residual on the silk is removed in heat treatment under 〉=160 ℃ of temperature.
8,, it is characterized in that under pressure with the water washing of boiling and dryly in a usual manner remove solvent residual on the silk by the described method of claim 6.
9, by the described method of claim 6, it is characterized in that under at least 300 ℃ of temperature, drawing.
10, by claim 1 and 6 described methods, it is characterized in that the inherent viscosity of polyamide-imides is 〉=0.8dl/g, be preferably 〉=0.9dl/g.
11, be the thermally-stabilised silk and the fiber of key component with the polyamide-imides, it is characterized in that they have:
-have an amide-imide chain (A) of following chemical formula:
-have an acid amides chain (B) of following chemical formula:
-have an acid amides chain (C) of following chemical formula:
-have an acid imide chain (D) of following chemical formula:
In the formula:
*Ar
1Represent toluylene or metaphenylene divalent aryl,
*Ar
2Represent the trivalent aryl,
*Ar
3Represent the tetravalence aryl,
*R represents divalent aryl,
*M represents alkali metal or alkaline-earth metal,
Chain (A) is 20-100%,
Chain (B) is 0-5%,
Chain (C) is 0 to＜100%,
Chain (D) is 0 to＜100%,
Chain (A)+(B)+(C)+(D) sum is 100%, and also keeps elastic modelling quantity at least 40% at 310 ℃.
12, by described silk of claim 11 and fiber, it is characterized in that the inherent viscosity of polyamide-imides is 〉=0.8dl/g, be preferably 〉=0.9dl/g.
13, by described silk of claim 11 and fiber, it is characterized in that chain (A) is 50-100%, chain (B) is 0-3%, and chain (C) is 0-50%, and chain (D) is 0-80%.
14, by described silk of claim 11 and fiber, it is characterized in that Ar
2Be base with following chemical formula:
15, by described silk of claim 11 and fiber, it is characterized in that R is the base with following chemical formula:
16, by described silk of claim 11 and fiber, it is characterized in that M is an alkali metal.
17,, it is characterized in that it is 50% at least that elastic modelling quantity keeps by described silk of claim 11 and fiber.
18,, it is characterized in that their fibre number≤1dtex by described silk of claim 11 and fiber.
19, contain the thermally-stabilised goods that right requires 11 described silks and fiber.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9116339 | 1991-12-24 | ||
| FR9116339A FR2685354B1 (en) | 1991-12-24 | 1991-12-24 | PROCESS FOR SPINNING POLYAMIDE-IMIDE (PAI) SOLUTIONS BASED ON TOLUYLENE OR METAPHENYLENE DIISOCYANATES AND FIBERS THUS OBTAINED. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1077760A true CN1077760A (en) | 1993-10-27 |
| CN1053235C CN1053235C (en) | 2000-06-07 |
Family
ID=9420660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN92113840A Expired - Lifetime CN1053235C (en) | 1991-12-24 | 1992-12-24 | A wiredrawing method of polyamide-imide and the fibre prepared thereby |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0549494B1 (en) |
| JP (2) | JP2607816B2 (en) |
| KR (1) | KR100198184B1 (en) |
| CN (1) | CN1053235C (en) |
| AT (1) | ATE164640T1 (en) |
| DE (1) | DE69224974T2 (en) |
| ES (1) | ES2113934T3 (en) |
| FR (1) | FR2685354B1 (en) |
| IL (1) | IL104198A (en) |
| MX (1) | MX9207511A (en) |
| TW (1) | TW218898B (en) |
| ZA (1) | ZA929951B (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7923002B2 (en) | 2002-09-06 | 2011-04-12 | L'oreal S.A. | Composition for coating keratin fibres comprising a tacky wax |
| DE60314963T2 (en) | 2002-09-06 | 2008-04-10 | L'oreal | A method of decorative treatment of the eyelashes with a coating agent containing a sticky wax |
| DE60335996D1 (en) | 2002-09-26 | 2011-03-24 | Oreal | LIPSTICK WITH A SEQUENCED POLYMER |
| MXPA03008714A (en) | 2002-09-26 | 2004-09-10 | Oreal | Sequenced polymers and cosmetic compositions comprising the same. |
| FR2860143B1 (en) | 2003-09-26 | 2008-06-27 | Oreal | COSMETIC COMPOSITION COMPRISING A SEQUENCE POLYMER AND A NON-VOLATILE SILICONE OIL |
| FR2866231B3 (en) | 2004-02-13 | 2005-12-16 | Oreal | KERATIN FIBER COATING COMPOSITION COMPRISING A COLLAR WAX AND FIBERS |
| US8728451B2 (en) | 2004-03-25 | 2014-05-20 | L'oreal | Styling composition comprising, in a predominantly aqueous medium, a pseudo-block polymer, processes employing same and uses thereof |
| FR2904320B1 (en) | 2006-07-27 | 2008-09-05 | Oreal | POLYMER SEQUENCES, AND PROCESS FOR THEIR PREPARATION |
| FR2939033B1 (en) | 2008-12-02 | 2012-08-31 | Oreal | COSMETIC COMPOSITION FOR MAKE-UP AND / OR CARE OF KERATINIC MATERIALS, AND METHOD FOR MAKE-UP |
| US10034829B2 (en) | 2010-10-27 | 2018-07-31 | Noxell Corporation | Semi-permanent mascara compositions |
| US9237992B2 (en) | 2009-10-27 | 2016-01-19 | The Procter & Gamble Company | Two-step mascara product |
| US9216145B2 (en) | 2009-10-27 | 2015-12-22 | The Procter & Gamble Company | Semi-permanent cosmetic concealer |
| US9004791B2 (en) | 2010-04-30 | 2015-04-14 | The Procter & Gamble Company | Package for multiple personal care compositions |
| US9173824B2 (en) | 2011-05-17 | 2015-11-03 | The Procter & Gamble Company | Mascara and applicator |
| EP2841163B1 (en) | 2012-04-26 | 2017-09-20 | Noxell Corporation | Two-step mascara product |
| US9140681B2 (en) | 2012-05-15 | 2015-09-22 | The Procter & Gamble Company | Method for quantitatively determining eyelash clumping |
| KR20150040930A (en) * | 2012-08-02 | 2015-04-15 | 다우 코닝 도레이 캄파니 리미티드 | Coating composition containing polyamide-imide resin |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1600067A (en) * | 1968-12-30 | 1970-07-20 | ||
| FR2045566A6 (en) * | 1969-05-23 | 1971-03-05 | Rhodiaceta | Thermostable filaments fibres from co-poly - amides |
| FR2079785A5 (en) * | 1970-02-12 | 1971-11-12 | Rhodiaceta | Lustrous polyamide-imide based fibres by new process |
| BE787500A (en) * | 1971-08-12 | 1973-02-12 | Rhone Poulenc Textile | PROCESS FOR OBTAINING SHINY WIRES |
| FR2636635B1 (en) * | 1988-09-21 | 1992-11-06 | Rhone Poulenc Sa | POLYAMIDE-IMIDE SOLUTIONS AND PROCESS FOR OBTAINING SAME |
| FR2643089B1 (en) * | 1988-09-21 | 1991-05-10 | Rhone Poulenc Fibres | POLYAMIDE-IMIDE-BASED YARNS AND PROCESS FOR OBTAINING SAME |
-
1991
- 1991-12-24 FR FR9116339A patent/FR2685354B1/en not_active Expired - Lifetime
-
1992
- 1992-12-18 TW TW081110176A patent/TW218898B/zh active
- 1992-12-21 AT AT92420475T patent/ATE164640T1/en not_active IP Right Cessation
- 1992-12-21 DE DE69224974T patent/DE69224974T2/en not_active Expired - Lifetime
- 1992-12-21 ES ES92420475T patent/ES2113934T3/en not_active Expired - Lifetime
- 1992-12-21 EP EP92420475A patent/EP0549494B1/en not_active Expired - Lifetime
- 1992-12-21 IL IL10419892A patent/IL104198A/en not_active IP Right Cessation
- 1992-12-22 ZA ZA929951A patent/ZA929951B/en unknown
- 1992-12-23 MX MX9207511A patent/MX9207511A/en unknown
- 1992-12-24 CN CN92113840A patent/CN1053235C/en not_active Expired - Lifetime
- 1992-12-24 JP JP4344752A patent/JP2607816B2/en not_active Expired - Lifetime
- 1992-12-24 KR KR1019920025530A patent/KR100198184B1/en not_active IP Right Cessation
-
1996
- 1996-04-24 JP JP8102845A patent/JP2726812B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ZA929951B (en) | 1993-06-28 |
| EP0549494B1 (en) | 1998-04-01 |
| IL104198A0 (en) | 1993-05-13 |
| DE69224974D1 (en) | 1998-05-07 |
| KR930013263A (en) | 1993-07-21 |
| JP2607816B2 (en) | 1997-05-07 |
| JPH06200413A (en) | 1994-07-19 |
| ATE164640T1 (en) | 1998-04-15 |
| IL104198A (en) | 1995-12-08 |
| KR100198184B1 (en) | 1999-06-15 |
| CN1053235C (en) | 2000-06-07 |
| ES2113934T3 (en) | 1998-05-16 |
| FR2685354B1 (en) | 1996-03-29 |
| FR2685354A1 (en) | 1993-06-25 |
| EP0549494A1 (en) | 1993-06-30 |
| TW218898B (en) | 1994-01-11 |
| JP2726812B2 (en) | 1998-03-11 |
| JPH08284017A (en) | 1996-10-29 |
| DE69224974T2 (en) | 1998-09-24 |
| MX9207511A (en) | 1994-05-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C15 | Extension of patent right duration from 15 to 20 years for appl. with date before 31.12.1992 and still valid on 11.12.2001 (patent law change 1993) | ||
| OR01 | Other related matters | ||
| C56 | Change in the name or address of the patentee |
Owner name: GUIMCRE CO.,LTD. Free format text: FORMER NAME OR ADDRESS: RHONE-POULENC FIBRES |
|
| CP01 | Change in the name or title of a patent holder |
Patentee after: Kermel SNC. Patentee before: Rhone-Poulenc Fibres |
|
| C17 | Cessation of patent right | ||
| CX01 | Expiry of patent term |
Expiration termination date: 20121224 Granted publication date: 20000607 |