CN1597727A - Solid state polymerization preparation method of liquid crystal copolyester - Google Patents
Solid state polymerization preparation method of liquid crystal copolyester Download PDFInfo
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- CN1597727A CN1597727A CN 200410054025 CN200410054025A CN1597727A CN 1597727 A CN1597727 A CN 1597727A CN 200410054025 CN200410054025 CN 200410054025 CN 200410054025 A CN200410054025 A CN 200410054025A CN 1597727 A CN1597727 A CN 1597727A
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- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 87
- 229920001634 Copolyester Polymers 0.000 title claims abstract description 33
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 33
- 239000007787 solid Substances 0.000 title claims abstract description 12
- 238000002360 preparation method Methods 0.000 title claims description 13
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims abstract description 40
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims abstract description 33
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims abstract description 26
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 13
- 239000007789 gas Substances 0.000 claims description 9
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 8
- 238000006068 polycondensation reaction Methods 0.000 claims description 7
- 230000035484 reaction time Effects 0.000 claims description 6
- UOBYKYZJUGYBDK-UHFFFAOYSA-N 2-naphthoic acid Chemical compound C1=CC=CC2=CC(C(=O)O)=CC=C21 UOBYKYZJUGYBDK-UHFFFAOYSA-N 0.000 claims description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052786 argon Inorganic materials 0.000 claims description 2
- 235000011089 carbon dioxide Nutrition 0.000 claims description 2
- 239000001307 helium Substances 0.000 claims description 2
- 229910052734 helium Inorganic materials 0.000 claims description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 2
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052754 neon Inorganic materials 0.000 claims description 2
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 17
- 230000004927 fusion Effects 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 16
- AVJMRDMDBOCDSE-UHFFFAOYSA-N C1(O)=CC(O)=CC=C1.C(C1=CC=C(C(=O)O)C=C1)(=O)O.C1=CC=CC2=CC(=CC=C12)C(=O)O Chemical compound C1(O)=CC(O)=CC=C1.C(C1=CC=C(C(=O)O)C=C1)(=O)O.C1=CC=CC2=CC(=CC=C12)C(=O)O AVJMRDMDBOCDSE-UHFFFAOYSA-N 0.000 description 14
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- XBNGYFFABRKICK-UHFFFAOYSA-N 2,3,4,5,6-pentafluorophenol Chemical compound OC1=C(F)C(F)=C(F)C(F)=C1F XBNGYFFABRKICK-UHFFFAOYSA-N 0.000 description 2
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- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachloro-phenol Natural products OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 241001411320 Eriogonum inflatum Species 0.000 description 1
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Abstract
A process for preparing liquid crystal copolyester by solid polymerization includes such steps as heating the prepolymer poly(parahydroxy benzoic acid/2,6-naphthalenediformic acid/terephthalic acid/hydroquinone) to a temp which is 10-60 deg.c lower than its fusion point, and solid polimerizing reaction under existance of inertial gas.
Description
Technical field
The invention belongs to the liquid crystal high polymer material technical field, be specifically related to a kind of THERMOTROPIC LIQUID CRYSTAL COPOLYESTER poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) solid state polymerization.
Technical background
THERMOTROPIC LIQUID CRYSTAL COPOLYESTER (TLCP) is a kind of high performance polymer material, have splendid over-all properties: good flowability, product precision size degree height, dimensional stability are good, low linear expansion coefficient, have high rigidity, high strength, high tenacity concurrently, the anti chemical properties as the pottery, remarkable resistance to air loss, high heat distortion temperature, agent of low hygroscopicity, inherent flame retardant resistance, good thermostability, good radiation-resistant property, vibration absorption.These excellent comprehensive performances make it become indispensable in many high-tech sectors, irreplaceable material.Be widely used in field of electronics (as various connectors, switch, printed-wiring board (PWB), unicircuit and transistorized encapsulated moulding product, video tape recorder parts, CD player parts, relay box, printer unit etc.), field fiber (as the secondary coating of optical fiber, tension member, coupling mechanism, junctor etc.), chemical industry equipment and device (making pump, valve, gauger component etc.) and other apparatus aspect etc. as replacing unmanageable fluoroplastics and stainless steel.
Though THERMOTROPIC LIQUID CRYSTAL COPOLYESTER has lot of advantages, traditional production technique---melt phase polycondensation need carry out under the high temperature high vacuum condition, the difficult control of reaction conditions; When melt phase polycondensation, polymerization reaction late stage, along with the prolongation in reaction times, the molecular weight of polymkeric substance improves, and melt viscosity is very high, and product is difficult for discharging; In addition, the high-temperature fusion polycondensation because polymerization temperature is higher, causes polymerisate seriously painted easily.For overcoming above-mentioned shortcoming, adopting solid state polymerization to synthesize liquid crystal copolyester is a good selection.The application of solid state polymerization in liquid crystal copolyester still is not reported.
Summary of the invention
The objective of the invention is to propose a kind of reaction conditions and be easy to control, the significantly reduced liquid crystal copolyester preparation method of product cost.
We know that solid-state polymerization is being lower than about 30 ℃ of prepolymer fusing points, is carrying out in the nitrogen atmosphere usually, and the relatively good control of reaction conditions obtains the high-molecular weight polymerisate easily, and the color and luster of polymerisate is more shallow.Solid state polymerization is applied in polyethylene terephthalate (PET) production process, and has obtained good effect.The present invention adopts solid state polymerization to prepare liquid crystal copolyester, and has explored corresponding technological conditions.
The inventive method is with P-hydroxybenzoic acid (HBA), Resorcinol (HQ), 2,6-naphthalic acid (NDA) and terephthalic acid (TA) are polymerization single polymerization monomer, the liquid crystal copolyester prepolymer that adopts the melt-polycondensation preparation to form earlier by these four kinds of components, adopt then solid state polymerization synthetic macromolecule amount poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) liquid crystal copolyester.
Among the present invention, the step that the employing melt-polycondensation prepares the liquid crystal prepolymer is as follows: in the stainless steel cauldron of mechanical stirrer, import and export of nitrogen, heating system, temperature control and the temperature measuring equipment of being furnished with the detection of band moment of torsion, add monomer and proper catalyst by monomer ratio cited below, under logical nitrogen and condition of stirring, progressively be warmed up to 350 ℃ with 1-3 ℃/min, under this temperature, continue reaction, viscosity until polymeric system reaches preset value (indicating with the moment of torsion electric current), finishes reaction.Take out the cooling back, pulverizes with pulverizer.(can referring to Chinese patent application CN1492023A).
After polycondensation, P-hydroxybenzoic acid in the prepolymer (HBA), Resorcinol (HQ), 2, the structural unit that 6-naphthalic acid (NDA) and terephthalic acid (TA) are drawn appears in the chain structure of liquid crystal prepolymer molecule with the form of following residue respectively:
The molar fraction of wherein controlling monomer HBA (I) is 50%-64%, the molar fraction of monomer HQ (II) is 17.5%-25%, the molar fraction of monomer NDA (III) is 10.5%-17.5%, and the molar fraction of monomer TA (IV) is 5.25%-10%, and total molar fraction satisfies 100%.Wherein 2, the more suitable ratio of the molar fraction of the molar fraction of 6-naphthalic acid (NDA) and terephthalic acid (TA) is: NDA/TA=60/40-70/30.
Be used for the inventive method poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) logarithmic viscosity number (I.V.) of liquid crystal copolyester prepolymer is at least 0.5dL/g, being advisable with 1.5 to 3.0dL/g, (Pentafluorophenol is made solvent, concentration is 0.1dL/g, uses determination of ubbelohde viscometer at 60 ℃).
Be used for our bright method poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) the liquid crystal copolyester prepolymer is columned particle.Cylinder diameter is advisable in the 0.5mm-4mm scope, and the particle length-to-diameter ratio is about 1: 0.5-0.5: 1.Preferable particle diameter is 1-2mm.This is because if particle is excessive, and solid-state polymerization carries out slowlyer; And particle is too small, easily bonds between particle during solid-state polymerization, and is unfavorable for that inert gas passes through.
The liquid crystal copolyester prepolymer carried out temperature programming process slowly: with the temperature rise rate of 2-5 ℃/min, be elevated to the solid-state polymerization temperature from room temperature before arriving the solid-state polymerization temperature of reaction.
Poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) the liquid crystal copolyester prepolymer, can certain temperature carry out solid-state polymerization or stage by stage temperature-raising method carry out solid-state polymerization.The inventive method adopts carries out solid-state polymerization in certain temperature.The solid-state polymerization temperature can be selected to the warm area of prepolymer fusing point in the lower bound temperature that just is higher than polymerization, and this temperature normally is lower than about 10 ℃ to 60 ℃ of prepolymer fusing point.Optimum solid-state polymerization temperature is less than about 15 ℃ to 50 ℃ of its fusing points greatly.Poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) the solid-state polymerization temperature of liquid crystal copolyester prepolymer is generally between 260 ℃ to 300 ℃.It is proper in most cases to carry out solid-state polymerization between 280 ℃ to 300 ℃.
The solid-state polymerization reaction is carried out in rare gas element usually, and adopts the mode of dynamic flow.Inert gas atmosphere not only can protect prepolymer to avoid thermooxidizing, and inert gas can remove the small molecules reactant, as acetic acid etc.Normally used inert gas flow is 6-120mL/min.The rare gas element that is applicable to the solid-state polymerization process can be nitrogen, carbonic acid gas, helium, neon, argon gas and some industrial gaseous waste etc., but uses nitrogen as rare gas element usually.
Poly-in order to make (P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) the liquid crystal copolyester prepolymer has use properties preferably through the final product of solid-state polymerization, needs the sufficiently long solid-state polymerization time.The solid-state polymerization time is generally 1 to 40 hour, and is comparatively suitable with 4 to 24 hours.
The present invention synthetic earlier low-molecular-weight poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) prepolymer, again with this prepolymer solid-state polymerization, generate high-molecular weight poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) liquid crystal copolyester.With respect to high-temperature fusion synthetic macromolecule amount poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) method of liquid crystal copolyester, method of the present invention has reduced the requirement to equipment, cost and energy consumption significantly reduce, reaction conditions is easy to control, the quality of product obtains to improve in addition, comprises the color and luster of product etc.
Relate to some analysis test methods in embodiments of the present invention, be described below.
Logarithmic viscosity number (I.M) is measured:
Solvent is a Pentafluorophenol.In cleaning exsiccant 25mL volumetric flask, be weighed into 0.025g poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) the liquid crystal copolyester sample, add this solvent of about 20mL with transfer pipet.Cover bottle stopper, volumetric flask is placed about 8 hours of 60 ℃ of water-baths, sample is dissolved fully, this solvent cut of using 60 ℃ then is to scale, join the solution of concentration C=0.1g/dL.This solution is filled in another cleaning exsiccant 25mL volumetric flask with No. 2 sand core funnels, and placed above-mentioned water-bath constant temperature 1 hour.In 60 ℃ of water-baths, survey the elution time t of neat solvent and solution respectively with Ubbelohde viscometer (capillary diameter is 0.5-0.6mm)
SolventAnd t
SolutionCalculate I.V. with following formula then:
Fusing point test:
Polymer samples is measured fusing point with dsc (DSC).Used instrument is TAInstruments DSC 910 thermal analyzers.Instrument is calibrated respectively with pure indium and pure zinc in advance.Amount of samples 4～6mg.Heat-up rate is 20 ℃/min, measures in nitrogen atmosphere.The melting point polymer temperature is obtained by the attached software processes of this instrument.
Because the solid-state polymerization product has experienced long isothermal crystal process in the solid-state polymerization process, in order to eliminate the influence of isothermal crystal, the melting temperature of DSC test gained adopts the data in the temperature-rise period second time among the present invention: sample is through being warmed up to for the first time 370 ℃ of constant temperature 0.5min, then reduce to room temperature with 10 ℃/min, be warmed up to 370 ℃ with 20 ℃/min again, obtain DSC heating curve for the second time, curve reads melting temperature thus.
Hardness and modulus test (nano impress method):
Nano-indenter test is to adopt lasting rigidity to measure (CSM) technology to carry out on the XP of MTS company nano impress meter.The sample of test is quenched to room temperature in the air then all 380 ℃ of fusions.Each sample carries out impression 20 times at least at different sites, and spacing is 50 μ m between per two impressions of interaction in order to avoid.
Description of drawings
The curve that the liquid crystal copolyester modulus that Fig. 1 obtains for nano-indenter test changes with depth of indentation.Before SSP represents the prepolymer sample among the embodiment 2, and 8h and 24h represent the polymerisate of solid-state polymerization reaction after 8 hours and 24 hours among the embodiment 2, and SSP represents solid-state polymerization.
The curve that the liquid crystal copolyester hardness that Fig. 2 obtains for nano-indenter test changes with depth of indentation.Before SSP and 8h, 24h implication are identical with Fig. 1.
Fig. 3 is the influence of temperature to the reaction of liquid crystal copolyester solid-state polymerization., ▲, ■, ● represent embodiment 1,2,3,4.
Fig. 4 is the influence of nitrogen flow to the reaction of liquid crystal copolyester solid-state polymerization.●, ■ represents embodiment 1,5.
Fig. 5 is the influence of size of particles to the reaction of liquid crystal copolyester solid-state polymerization.●, ■ represents embodiment 1,6.
Embodiment
Embodiment 1
Present embodiment illustrated according to the present invention and gathered (P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) method of liquid crystal copolyester prepolymer solid-state polymerization.P-hydroxybenzoic acid in the prepolymer (HBA), 2, the mole proportioning of 6-naphthalic acid (NDA), Resorcinol (HQ) and terephthalic acid (TA) is 50/25/15/10, and the I.V. of prepolymer is that 1.5dL/g, fusing point are 312.4 ℃, and particle dia is 1.1mm.Prepolymer, is got 10g and placed tubulose solid-state polymerization device after 4 hours 110 ℃ of vacuum-dryings, feed nitrogen, be raised to 300 ℃, begin the solid-state polymerization of prepolymer then with the heat-up rate of 3 ℃/min.After arriving the setting polymerization time, under the situation of logical nitrogen, solid-state polymerization device cool to room temperature in air.Nitrogen flow is 60mL/min in the present embodiment.Fusing point and I.V. through different solid-state polymerization reaction times post polymerization product list in table 1.
The fusing point of table 1 solid-state polymerization reaction times and polymerisate and logarithmic viscosity number relation
| The solid-state polymerization time (h) | Fusing point (℃) | ????I.V.(dL/g) |
| 0 | ????312.4 | ????1.53 |
| 2 | ????319.1 | ????2.62 |
| 4 | ????321.7 | ????3.26 |
| 8 | ????322.7 | ????3.41 |
| 16 | ????323.2 | ????4.47 |
| 24 | ????323.9 | ????5.19 |
Through solid-state polymerization reaction in 24 hours, the logarithmic viscosity number I.V. of polymerisate was 5.19dL/g.Show solid state polymerization among the present invention can make high-molecular weight poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) liquid crystal copolyester.In addition, can see that in the certain molecular weight scope, fusing point also can be used to characterize the level of response of prepolymer solid-state polymerization by table 1 fusing point data.Comparatively speaking, measure fusing point with DSC and represent that the level of response of solid-state polymerization is easier.
Embodiment 2
Experimental technique is with embodiment 1, but this embodiment solid-state polymerization temperature of reaction is 280 ℃.Under this temperature condition, list in table 2 through the fusing point of different time solid-state polymerization reaction post polymerization product.The product of prepolymer and solid-state polymerization reaction 8 hours and 24 hours is carried out nano-indenter test, and test result sees Table 3 and accompanying drawing 1,2.
The fusing point relation of table 2 solid-state polymerization reaction times and polymerisate
| Polymerization time (h) | Fusing point (℃) |
| ????0 | ????312.4 |
| ????2 | ????315.1 |
| ????4 | ????317.5 |
| ????8 | ????319.7 |
| ????16 | ????320.8 |
| ????24 | ????322.0 |
The modulus and the hardness of polymkeric substance before and after table 3 solid-state polymerization
| Before the solid-state polymerization | 280 ℃ of solid- | 280 ℃ of solid- | |
| Modulus (GPa) | ??2.27±0.37 | ????2.62±0.26 | ????2.73±0.16 |
| Hardness (GPa) | ??0.13±0.04 | ????0.16±0.02 | ????0.18±0.02 |
This embodiment show solid state polymerization of the present invention can significantly improve poly-(P-hydroxybenzoic acid 2, the 6-naphthalic acid terephthalic acid Resorcinol) molecular weight of liquid crystal copolyester, its mechanical property (hardness and modulus) also is greatly improved thereupon.
Embodiment 3,4
Experimental technique is with embodiment 1.When having investigated 240 ℃ and 260 ℃ of solid-state polymerizations, the variation of melting point situation of polymerisate.Under embodiment 1 and 2, four different solid-state polymerization temperature of reaction, melting point polymer is shown in the accompanying drawing 3 with the change list of solid-state polymerization time.As seen from Figure 3,240 ℃ of reaction fusing points do not change, and along with the raising of solid-state polymerization temperature of reaction, speed of reaction increases, and reach the required time shortening of estimating the fusing point product, thereby the fusing point of product raise fast.This shows that the solid-state polymerization reaction of temperature range can carry out to(for) this prepolymer is 260-300 ℃, and comparatively suitable with 280-300 ℃.
Experimental technique is with embodiment 1.Nitrogen flow is 10mL/min.In conjunction with the embodiments 1, investigate solid-state polymerization response situation under these two different nitrogen flows, the polymerisate fusing point is illustrated in the accompanying drawing 4.By accompanying drawing 4 as seen, nitrogen flow is big, and the polymerisate fusing point raises very fast, but along with the increase in reaction times, final fusing point reaches unanimity.
Embodiment 6
Experimental technique is with embodiment 1.Particle dia is 2.1mm, and nitrogen flow is the solid-state polymerization response situation of 60mL/min.Carrying out the reacted product fusing point of solid-state polymerization data under 1, two particle diameter in conjunction with the embodiments is illustrated in the accompanying drawing 5.As seen from Figure 5, small-particle solid-state polymerization speed of response is fast.Explanation is than the favourable solid-state polymerization of small-particle, shortens the time of solid-state polymerization reaction, but too small-particle bonds easily, also is unfavorable for that inert gas the flowing of particle surface, can reduce the solid-state polymerization speed of response on the contrary.Therefore, adopt the size of particles of the inventive method proper.
Embodiment 7
Experimental technique is with embodiment 1.The mol ratio of HBA, HQ, NDA and TA is: 60/20/14/6, and the I.V. of prepolymer is 1.0dL/g, and particle dia is 3mm, and heat-up rate is 2 ℃/min, and the solid-state polymerization temperature of reaction is 280 ℃.Under this condition after different time solid-state polymerization reaction, the fusing point of polymerisate approaches the data of fusing point shown in the table 1.
Claims (9)
1, a kind of liquid crystal copolyester prepolymer preparation method, it is characterized in that with P-hydroxybenzoic acid (HBA), Resorcinol (HQ), 2,6-naphthalic acid (NDA) and terephthalic acid (TA) are polymerization single polymerization monomer, adopt the synthetic liquid crystal copolyester prepolymer of melt-polycondensation earlier, adopt the solid-state polymerization method to synthesize liquid crystal copolyester then, wherein the molar fraction of HBA component is 50%-65%, the molar fraction of HQ component is 17.5%-25%, the molar fraction of NDA component is 10.5%-17.5%, and the molar fraction of TA component is 5.25%-10%.
2, preparation method according to claim 1 is characterized in that 2, and the molar fraction of 6-naphthalic acid with the ratio of the molar fraction of terephthalic acid is: 60/40-70/30.
3, preparation method according to claim 1 is characterized in that in solid state polymerization, and the solid-state polymerization temperature is lower than 10-60 ℃ of described prepolymer fusing point, and described prepolymer is cylindric, and diameter is 0.5mm-4mm, and length-to-diameter ratio is 1: 0.5-0.5: 1.
4, preparation method according to claim 3, the logarithmic viscosity number scope that it is characterized in that described cylindrical shape prepolymer is 0.5-3.0dL/g.
5, preparation method according to claim 3 is characterized in that the heat-up rate of described liquid crystal copolyester prepolymer with 2-5 ℃/min, is heated to the solid-state polymerization temperature from room temperature.
6, preparation method according to claim 3 is characterized in that described solid-state polymerization temperature is 260-300 ℃.
7, preparation method according to claim 1 is characterized in that in the solid-state polymerization method that solid-state polymerization is reflected at rare gas element and exists down and carry out, and employing rare gas element dynamic flow mode.
8, preparation method according to claim 7 is characterized in that described rare gas element is one or more of nitrogen, carbonic acid gas, helium, neon or argon gas; The flow of rare gas element is 6-120mL/min.
9, preparation method according to claim 1 is characterized in that the described solid-state polymerization reaction times is 1-40 hour.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200410054025 CN1257927C (en) | 2004-08-26 | 2004-08-26 | Solid state polymerization preparation method of liquid crystal copolyester |
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| CN 200410054025 CN1257927C (en) | 2004-08-26 | 2004-08-26 | Solid state polymerization preparation method of liquid crystal copolyester |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102250622A (en) * | 2011-08-15 | 2011-11-23 | 金发科技股份有限公司 | Method for preparing material with low flowability |
| CN101681073B (en) * | 2007-10-31 | 2012-12-05 | Dic株式会社 | Method for producing liquid crystal composition |
| CN102816308A (en) * | 2012-08-09 | 2012-12-12 | 东华大学 | Preparation method of thermotropic liquid crystal polyarylate |
| WO2014036760A1 (en) * | 2012-09-06 | 2014-03-13 | 金发科技股份有限公司 | Liquid crystal polyester and preparation method thereof, composition containing the same and use of composition |
| CN109535406A (en) * | 2017-09-22 | 2019-03-29 | 宁波聚嘉新材料科技有限公司 | The preparation method of polyarylate of the one kind based on 2- (3- hydroxy phenyl) -6- carboxyl pyridine and imidazoles |
| CN109734891A (en) * | 2018-12-28 | 2019-05-10 | 江苏沃特特种材料制造有限公司 | Modified aromatic race liquid-crystal polyester resin with less anisotropy and preparation method thereof |
| CN110181829A (en) * | 2019-05-27 | 2019-08-30 | 陈祚 | A kind of liquid crystal polyester thin film industrial manufacture process |
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2004
- 2004-08-26 CN CN 200410054025 patent/CN1257927C/en not_active Expired - Lifetime
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101681073B (en) * | 2007-10-31 | 2012-12-05 | Dic株式会社 | Method for producing liquid crystal composition |
| CN102250622A (en) * | 2011-08-15 | 2011-11-23 | 金发科技股份有限公司 | Method for preparing material with low flowability |
| CN102250622B (en) * | 2011-08-15 | 2013-09-04 | 金发科技股份有限公司 | Method for preparing material with low flowability |
| CN102816308A (en) * | 2012-08-09 | 2012-12-12 | 东华大学 | Preparation method of thermotropic liquid crystal polyarylate |
| CN102816308B (en) * | 2012-08-09 | 2014-06-18 | 东华大学 | Preparation method of thermotropic liquid crystal polyarylate |
| WO2014036760A1 (en) * | 2012-09-06 | 2014-03-13 | 金发科技股份有限公司 | Liquid crystal polyester and preparation method thereof, composition containing the same and use of composition |
| CN103665354A (en) * | 2012-09-06 | 2014-03-26 | 金发科技股份有限公司 | Liquid crystal polyester, preparation method and composition thereof as well as application of composition thereof |
| CN103665354B (en) * | 2012-09-06 | 2016-04-20 | 金发科技股份有限公司 | The application of a kind of liquid crystal polyester, its preparation method, its composition and composition thereof |
| CN109535406A (en) * | 2017-09-22 | 2019-03-29 | 宁波聚嘉新材料科技有限公司 | The preparation method of polyarylate of the one kind based on 2- (3- hydroxy phenyl) -6- carboxyl pyridine and imidazoles |
| CN109734891A (en) * | 2018-12-28 | 2019-05-10 | 江苏沃特特种材料制造有限公司 | Modified aromatic race liquid-crystal polyester resin with less anisotropy and preparation method thereof |
| CN110181829A (en) * | 2019-05-27 | 2019-08-30 | 陈祚 | A kind of liquid crystal polyester thin film industrial manufacture process |
| CN110181829B (en) * | 2019-05-27 | 2021-04-02 | 陈祚 | Industrial production process of liquid crystal polyester film |
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| CN1257927C (en) | 2006-05-31 |
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