WO1988007068A2 - Molding compositions comprising reinforced filled wholly aromatic polyesters - Google Patents

Molding compositions comprising reinforced filled wholly aromatic polyesters Download PDF

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Publication number
WO1988007068A2
WO1988007068A2 PCT/US1988/000818 US8800818W WO8807068A2 WO 1988007068 A2 WO1988007068 A2 WO 1988007068A2 US 8800818 W US8800818 W US 8800818W WO 8807068 A2 WO8807068 A2 WO 8807068A2
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Prior art keywords
molding composition
wholly aromatic
component comprises
percent
aromatic polyester
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PCT/US1988/000818
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French (fr)
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WO1988007068A3 (en
Inventor
Paul David Frayer
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Dart Industries Inc.
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Publication of WO1988007068A2 publication Critical patent/WO1988007068A2/en
Publication of WO1988007068A3 publication Critical patent/WO1988007068A3/en

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/60Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
    • C08G63/605Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds the hydroxy and carboxylic groups being bound to aromatic rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013Fillers, pigments or reinforcing additives

Abstract

This invention provides molding compositions which comprise reinforced filled wholly aromatic polyesters and which can be molded into useful articles having low warpage values and good tensile strengths.

Description

MOLDING COMPOSITIONS COMPRISING REINFORCED FILLED WHOLLY AROMATIC POLYESTERS
This invention relates to molding compositions comprising reinforced filled wholly aromatic polyesters. More particularly, this invention relates to molding compositions comprising reinforced filled wholly aromatic polyesters which can be molded into articles having low warpage values and tensile strengths of at least 10,000 pounds per square inch.
Wholly aromatic polyesters are known to be self-reinforcing. Attempts to provide additional reinforcement, such as with glass fibers, have not been successful because the reinforcing component has a tendency to decrease the self-reinforcement of the wholly aromatic polyesters. Additionally, the use of a reinforcing component may not provide compositions which have significantly better properties. In some instances, these properties may be worse than the wholly aromatic polyester without the reinforcing component.
Wholly aromatic polyesters, with or without a reinforcing component, typically have a high level of anisotropy which can lead to warpage and to unacceptable molded articles. A decrease in the warpage values of wholly aromatic polyesters can be attained through the use of fillers. However, the use of fillers can lead to a decrease in the mechanical properties (such as tensile strength) of the molded articles.
These concepts are discussed by H. Voss and K. Friedrich, Journal of Materials Science, Volume 26 (1986), pp. 2889-2900 and L. K. English in Mechanical Engineering, March 1986, pp. 36-41.
Therefore, a need exists to provide a reinforced filled wholly aromatic polyester which can be molded into useful articles having good mechanical properties (such as tensile strength and impact strength) and low warpage values.
Accordingly, an object of this invention is to provide useful molding compositions which comprise wholly aromatic polyesters.
Another object of this invention is to provide useful molding compositions which comprise reinforced filled wholly aromatic polyesters.
Another object of this invention is to provide such compositions which can be molded into useful articles having good mechanical properties, such as tensile strength and impact strength.
Another object of this invention is to provide such compositions which can be molded into useful articles having low warpage values.
These and other objects, features and advantages of this invention, will become apparent from the following detailed description.
In accordance with the present invention, molding compositions are provided which comprise:
(a) from about 60 to about 80 percent, by volume, of a wholly aromatic polyester component;
(b) from about 10 to about 20 percent, by volume, of a reinforcing component; and
(c) from about 10 to about 30 percent, by volume, of a filler component, wherein an article molded from the composition exhibits a low warpage value and a tensile strength of at least 10,000 pounds per square inch and wherein the sum of components (b) and (c) is from about 20 to about 40 percent, by volume.
The tensile strengths recited in this application are determined by the ASTM D-638 method.
The warpage values recited in this application are determined by the following method:
A composition is molded into a connector having dimensions of about 4.65" length, .6" width and .285" thickness. The connector is placed on a flat surface, and the warpage is observed along the length direction of the connector, with the width direction at right angles to the flat surface. The amount of warpage is measured at the center of the connector by determining the distance (in mils) between the center and the flat surface.
In this method, warpage is measured twice. The first measurement ("as-molded") is taken immediately after the connector is molded. The second measurement is taken after heating the connector in an oven at 500°F. for 10 minutes to simulate soldering conditions.
As used in this application, the term "low warpage" means a value which is less than about 5 mils as-molded (first measurement) and less than about 15 mils after thermal treatment at 500°F. for 10 minutes (second measurement).
The wholly aromatic polyesters useful in this invention have melting temperatures of between about 200°C. and 450°C and comprise repeating units of one or more of the following formulas:
Figure imgf000005_0001
Figure imgf000006_0001
where X is -O-, -S-, -CO-, or -SO2-, and m and n are independently zero or one, and the total of the integers p + q + r + s + t + u is from approximately 3 to about 800.
In the most general combination, all of the units of the above formula can be present in a single polyester. A simple embodiment would be homopolymers of units I or IV. The preferred locations of the functional groups are in the para (1,4) and meta (1.3) positions. With respect to the naphthalene moiety, the preferred locations of the functional groups are 1,4; 1,5 and 2,6.
The symbols p, q, r, s, t, and u are integers and indicate the number of moieties present in the polyester. The total (p + q + r + s + t + u) can vary from 3 to 800 and, when present, the ratio of q:r, q:u, t:r, t:u, q+t:r, q+t:r+u, and t:r+u, of the moieties can vary from about 10:11 to about 11:10, with the most preferable ratio being 10:10.
Exemplary of monomers from which the moieties of formula I may be obtained are: p - hydroxybenzoic acid, phenyl-p- hydroxybenzoate, p-acetoxybenzoic acid and isobutyl-p- acetoxybenzoate. Those monomers from which the moiety of formula II may be obtained include terephthalic acid, isophthalic acid, diphenyl terephthalate, diethyl isophthalate , methylethyl terephthalate and the isobutyl half ester of terephthalic acid. Among the monomers from which the moiety of formula III results are: p,p'-biphenol; p,p'-oxybiphenol; 4'-dihydroxybenzophenone; resorcinol and hydroquinone.
Examples of monomers represented by formula IV are: 4- hydroxy-1-naphthoic acid; 5 acetoxy-1-naphthoic acid; and phenyl 5-hydroxy-1-naphthoate. Monomers representing formula V include: 1, 4-naphthalene dicarboxylic acid; 1, 5-naphthalene dicarboxylic acid and 2, 6-naphthalene dicarboxylic acid. The diphenyl esters or dicarbonyl chlorides of these acids can also be used. Examples of the monomers representative of the formulas VI are 1, 4-dihydroxynaphthalene; 2, 6-diacetoxynaphthalene and 1, 5-dihydroxynaphthalene.
A preferred class of polyesters has recurring units of formulas VII, VIII, and IX:
Figure imgf000008_0001
wherein the total of the integers p + q + r is about 3 to 800, the carbonyl groups of the moiety of formula VII or V III are linked to the oxy groups of the moiety of formula VII or IX; and the oxy groups of the moiety of formula VII or IX are linked to the carbonyl groups of the moiety of formula VII or VIII.
The polyesters of this invention comprise the precursor formulas VII, VIII and IX wherein the molar ratios are from 0.01:1:1 to 99:1:1 and preferably from 1:1:1 to 5:1:1.
Methods for the synthesis of these wholly aromatic polyesters are described in Cottis et al. U.S. Patents 3,637,595 and 4,563,508 and in Finestone U.S. Patent Application Serial No. 06/556,485, filed November 30, 1983.
Examples of reinforcing components useful in this invention are glass fibers, carbon fibers and graphite fibers. A preferred reinforcing component comprises glass fibers.
A useful range of the reinforcing component is from about 10 to 20 percent, by volume, based on the molding composition.
Examples of filler components useful in this invention are talc, aluminum powder, calcium sulfate, wollastonite, inert inorganic pigments, inorganic silicates and carbon black. A preferred filler component comprises talc, calcium sulfate or carbon black. A useful range of the filler component is from about 10 to 30 percent, by volume, based on the molding composition. A preferred range is from about 10 to 20 percent, by volume.
Within the scope of this invention, the wholly aromatic polyester, reinforcing and filler components may comprise a combination of two or more of these materials.
An important feature of this invention is that the combination of reinforcing and filler components is from about 20 to 40 percent, by volume, based on the molding composition, and preferably from about 27 to 33 percent, by volume. Amounts not within this range generally do not provide an acceptable tensile and impact strengths and low warpage value for the molded articles.
The compositions of this invention can be molded, by conventional techniques, into articles which have good mechanical properties, such as dimensional stability, tensile strength and thermal stability. Example of these articles include connectors for use in the electrical/electronics industry.
With regard to selected electronic applications, electrically conductive filler materials (such as certain aluminum powders and carbon blacks) can be used to great advantage.
The wholly aromatic polyesters useful in the present invention can also be chemically modified by various means such as by inclusion in the polyester of monofunctional reactants such as benzoic acid or a higher functional reactant such as trimesic acid or cyanuric chloride. The benzene rings in these polyesters are preferably unsubstituted but can be substituted with noninterferring substituents, examples of which include halogens (such as chlorine or bromine), lower alkoxy groups (such as methoxy), and lower alkyl groups (such as methyl and ethyl).
The invention is further illustrated by the following exampless which are illustrative of certain embodiments designed to teach those of ordinary skill in the art how to practice the invention and to represent the best mode contemplated for carrying out the invention. The wholly aromatic polyesters are prepared by conventional polycondensation methods and formulated with reinforcing and filler materials into molding compositions shown as Examples 1-7 in the following Table. The resulting compositions are molded into electrical connectors, and the tensile strengths and warpage values are shown in the Table.
The Table shows that Examples 3, 4 and 5 have acceptable tensile strengths and warpage values.
Examples 1 and 2 have good tensile strengths but do not have acceptable warpage values in both measurements.
Examples 6 and 7 have acceptable tensile strengths, but the warpage values were not measured as with Examples 1-5. These two examples were molded into large frames, and visual observations showed the warpage to be low and, therefore, acceptable.
In Examples 1-7, the wholly aromatic polyester component comprises two wholly aromatic polyesters. The first polyester is made from p-hydroxybenzoic acid; 4,4'- dihydroxybiphenyl; and terephthalic acid in the molar ratio of 2:1:1. The second polyester is made from p-hydroxybenzoic acid; 4,4'- dihydroxybiphenyl; and isophthalic acid in the molar ratio of 3.7:1:1, and is used in an amount of less than 5%, by weight, based on the total molding composition.
Example 8
A composition is made from 12.8 volume percent glass fiber, 19.7 volume percent talc and 67.5 volume percent of a wholly aromatic polyester component comprising two wholly aromatic polyesters. The first polyester is made from p-hydroxybenzoic acid; 4,4'-dihydroxybiphenyl and terephthalic acid in the molar ratios of 2:1:1, respectively, and the second polyester is made from p-hydroxybenzoic acid; 4,4'-dihydroxybyphenyl, terephthalic acid and isophthalic acid in the molar ratios of 3:1:0.75:0:25, respectively. The second polyester is used in an amount equal to 10.0 percent by weight based on the total molding composition. Molded parts from this composition demonstrated excellent impact strength and low warpage.
The foregoing description relates to certain embodiments of the present invention, and modifications or alterations may be made without departing from the spirit and scope of the invention as set forth in the claims.
Figure imgf000018_0001
Figure imgf000019_0001

Claims

1. A molding composition comprising:
(a) from about 60 to about 80 percent, by volume, of a wholly aromatic polyester component;
(b) from about 10 to about 20 percent, by volume, of a fibrous reinforcing component; and
(c) from about 10 to about 30 percent, by volume, of a filler component, wherein an article molded from the composition exhibits low warpage value and a tensile strength of at least 10,000 pounds per square inch and wherein the sum of components (b) and (c) is from about 20 to about 40 percent, by volume.
2. A molding composition as defined by Claim 1 wherein the wholly aromatic polyester component is an oxybenzoyl copolyester.
3. A molding composition as defined by Claim 1 wherein the wholly aromatic polyester component comprises repeating units of one or more of the following formulas:
Figure imgf000012_0001
Figure imgf000013_0001
Figure imgf000013_0002
Figure imgf000013_0003
Figure imgf000013_0004
where X is -O-, -S-, -CO-, or -SO2; and m and n are independently zero or one, and the total of the integers p + q + r + s + t + u is from approximately 3 to about 800.
4. A molding composition as defined by Claim 3 wherein each of the ratios q:r, q:u, t:r, t:u, q+t:r, q+t:r+u, and t:r+u, of the moieties present, is about 10:11 to about 11:10.
5. A molding composition as defined by Claim 4 wherein each of the ratios is about 10:10.
6. A molding composition as defined by Claim 3 wherein n is zero.
7. A molding composition as defined by Claim 1 wherein the wholly aromatic polyester component comprises repeating units of one or more of the following formulas:
wherein the total of the integers p + q + r is about 3 to 800, the carbonyl groups of the moiety of formula VII or VIII are linked to the oxy groups of the moiety of formula VII or IX; and the oxy groups of the moiety of formula VII or IX are linked to the carbonyl groups of the moiety of formula VII or VIII.
8. A molding composition as defined by Claim 7 wherein the wholly aromatic polyester component comprises repeating units of formulas VII, VIIl and IX, wherein the molar ratios are from 0.01:1:1 to 99:1:1, respectively.
9. A molding composition as defined by Claim 7 wherein the wholly aromatic polyester component comprises repeating units of formulas VII, VIII and IX, wherein the molar ratios are from 1:1:1 to 5:1:1, respectively.
10. A molding composition as defined by Claim 7 wherein the wholly aromatic polyester component comprises repeating units of formulas VII, VIII and IX, wherein the molar ratios are 2:1:1 respectively.
11. A molding composition as defined by Claim 1 wherein the fibrous reinforcing component is glass fibers.
12. A molding composition as defined by Claim 1 wherein the reinforcing component is carbon fibers.
13. A molding composition as defined by Claim 1 wherein the filler component is talc.
14. A molding composition as defined by Claim 1 wherein the filler component is carbon black.
15. A molding composition as defined by Claim 1 wherein the filler component is aluminum powder.
16. A molding composition as defined by Claim 1 wherein the sum of components (b) and (c) is from about 27 to about 33 percent, by volume.
17. A molding composition as defined by Claim 1 wherein wholly aromatic polyester component comprises a combination of two wholly aromatic polyesters.
18. A molding composition as defined by Claim 17 wherein the wholly aromatic polyesters are made from (a) p-hydroxybenzoic acid; 4,4'-dihydroxybiphenyl; and terephthalic acid in the molar ratio of 2:1:1 and (b) p-hydroxybenzoic acid; 4,4 -dihydroxybiphenyl; and isophthalic acid in the molar ratio of 3.7:1:1.
19. A molding composition as defined by Claim 18 wherein the polyester made from isophthalic acid is present in an amount up to about 7 percent, by weight, based on the total molding composition.
20. A molding composition as defined by Claim 17 wherein the wholly aromatic polyesters are made from (a) p-hydroxybenzoic acid; 4,4'-dihydroxybiphenyl; and terephthalic acid in the molar ratio of 2:1:1 and (b) p-hydroxybenzoic acid; 4,4'-dihydroxybiphenyl; terephthalic acid; and isophthalic acid in the molar ratio of 3:1:0.75:0.25.
21. A molding composition as defined by Claim 20 wherein the polyester made from both terephthalic and isophthalic acids is present in an amount up to about 15 percent, by weight, based on the total molding composition.
22. A molding composition as defined by Claim 1 wherein the filler component comprises a combination of talc and carbon black.
23. A molding composition as defined by Claim 1 wherein the filler component comprises a combination of calcium sulfate and carbon black.
24. A molding composition as defined by Claim 1 wherein the filler component comprises talc; the reinforcing component comprises glass fibers; the sum of components (b) and (c) is from about 27 to about 33 percent, by volume; and the wholly aromatic polyester component comprises repeating units of formulas VII, VIII and IX.
25. A molding composition as defined by Claim 1 wherein the filler component comprises calcium sulfate and conductive carbon black; the reinforcing component comprises milled glass fibers; the sum of components (b) and (c) is from about 27 to about 33 percent, by volume; and the wholly aromatic polyester component comprises repeating units of formulas VII, VIII and IX.
26. A molding composition as defined by Claim 1 wherein the filler component comprises talc and conductive carbon black; the reinforcing component comprises glass fibers; the sum of components (b) and (c) is from about 27 to about 33 percent, by volume; and the wholly aromatic polyester component comprises repeating units of formulas VII, VIII and IX.
PCT/US1988/000818 1987-03-20 1988-03-18 Molding compositions comprising reinforced filled wholly aromatic polyesters WO1988007068A2 (en)

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US028,306 1987-03-20

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0482639A2 (en) * 1990-10-24 1992-04-29 E.I. Du Pont De Nemours And Company Thermotropic liquid crystalline polyesters from 2-methylhydroquinone
EP0630955A1 (en) * 1993-06-25 1994-12-28 Sumitomo Chemical Company, Limited Liquid crystal polyester resin composition and lamp reflector

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US4267289A (en) * 1980-07-03 1981-05-12 Celanese Corporation Blend of wholly aromatic polyesters
JPS5710641A (en) * 1980-06-24 1982-01-20 Sumitomo Chem Co Ltd Wholly aromatic copolyester resin composition
US4318841A (en) * 1980-10-06 1982-03-09 Celanese Corporation Polyester of 6-hydroxy-2-naphthoic acid, para-hydroxy benzoic acid, terephthalic acid, and resorcinol capable of readily undergoing melt processing to form shaped articles having increased impact strength
US4375530A (en) * 1982-07-06 1983-03-01 Celanese Corporation Polyester of 2,6-naphthalene dicarboxylic acid, 2,6-dihydroxy naphthalene, terephthalic acid, and hydroquinone capable of forming an anisotropic melt
EP0261869A2 (en) * 1986-09-26 1988-03-30 Sumitomo Chemical Company, Limited Synthetic resin composition containing a polyarylate and a polyester
EP0264290B1 (en) * 1986-10-17 1994-01-26 Polyplastics Co. Ltd. Composition for injection moulding

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JPS5710641A (en) * 1980-06-24 1982-01-20 Sumitomo Chem Co Ltd Wholly aromatic copolyester resin composition
US4267289A (en) * 1980-07-03 1981-05-12 Celanese Corporation Blend of wholly aromatic polyesters
US4318841A (en) * 1980-10-06 1982-03-09 Celanese Corporation Polyester of 6-hydroxy-2-naphthoic acid, para-hydroxy benzoic acid, terephthalic acid, and resorcinol capable of readily undergoing melt processing to form shaped articles having increased impact strength
US4375530A (en) * 1982-07-06 1983-03-01 Celanese Corporation Polyester of 2,6-naphthalene dicarboxylic acid, 2,6-dihydroxy naphthalene, terephthalic acid, and hydroquinone capable of forming an anisotropic melt
EP0261869A2 (en) * 1986-09-26 1988-03-30 Sumitomo Chemical Company, Limited Synthetic resin composition containing a polyarylate and a polyester
EP0264290B1 (en) * 1986-10-17 1994-01-26 Polyplastics Co. Ltd. Composition for injection moulding

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0482639A2 (en) * 1990-10-24 1992-04-29 E.I. Du Pont De Nemours And Company Thermotropic liquid crystalline polyesters from 2-methylhydroquinone
EP0482639A3 (en) * 1990-10-24 1992-11-19 E.I. Du Pont De Nemours And Company Thermotropic liquid crystalline polyesters from 2-methylhydroquinone
EP0630955A1 (en) * 1993-06-25 1994-12-28 Sumitomo Chemical Company, Limited Liquid crystal polyester resin composition and lamp reflector
US5529716A (en) * 1993-06-25 1996-06-25 Sumitomo Chemical Company, Limited Liquid crystal polyester resin composition and lamp reflector

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PT87028A (en) 1988-04-01
IL85788A0 (en) 1988-09-30
JPH01502833A (en) 1989-09-28
WO1988007068A3 (en) 1988-12-29
PT87028B (en) 1992-06-30
EP0312585A1 (en) 1989-04-26
AU1780388A (en) 1988-10-10

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