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Liquid-crystal polyester resin composition

A technology of resin composition and liquid crystal polyester, applied in the directions of liquid crystal materials, chemical instruments and methods, etc., can solve the problems of easy change, reduced productivity of the molded body, long cooling time, etc., and achieves stable plasticizing time and stable molding process. Effect

Active Publication Date: 2019-06-07
SUMITOMO CHEM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, in the case of liquid crystal polyester resin compositions, the plasticizing time is unstable and easily fluctuates, and may be longer than the cooling time
In this case, it is difficult to perform molding with a constant cycle, and the productivity of molded objects may decrease.

Method used

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  • Liquid-crystal polyester resin composition
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Examples

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Embodiment

[0262] Hereinafter, the present invention will be further described in detail by using specific examples. However, this invention is not limited at all by the Example shown below.

[0263] In addition, in this Example and a comparative example, the volume average particle diameter, a melting point, and a particle shape were measured by the following methods, respectively.

[0264]

[0265] The volume average particle diameter was measured by the laser diffraction method under the following conditions.

[0266] Measurement conditions

[0267] Measuring device: laser diffraction / scattering particle size distribution measuring device (manufactured by HORIBA Co., Ltd.; LA-950V2);

[0268] Refractive index of particles: 1.53-0.1i;

[0269] Dispersion medium: water;

[0270] Dispersion medium refractive index: 1.33.

[0271]

[0272] The melting point was measured using a differential thermal analyzer (manufactured by Shimadzu Corporation; DTA-50). The endothermic peak tem...

manufacture example 1

[0301] Add p-hydroxybenzoic acid (994.5 g, 7.20 moles), terephthalic acid (272.1 g, 1.64 moles), isophthalic acid (272.1 g, 1.64 moles) and Formic acid (126.6 g, 0.76 mol), 4,4'-dihydroxybiphenyl (446.9 g, 2.40 mol), and 1347.6 g (13.20 mol) of acetic anhydride. After replacing the gas in the reactor with nitrogen, 0.18 g of 1-methylimidazole was added, and the temperature was raised from room temperature to 150° C. over 30 minutes while stirring under nitrogen flow, and refluxed at 150° C. for 30 minutes.

[0302] Then, after adding 2.4 g of 1-methylimidazole, while distilling off by-produced acetic acid and unreacted acetic anhydride, the temperature was raised from 150° C. to 320° C. over 2 hours and 50 minutes. To complete the reaction, the contents were taken out from the reactor and cooled to room temperature to obtain a prepolymer (solid matter).

[0303] Then, the prepolymer was pulverized using a pulverizer, and the obtained pulverized product was heated from room te...

manufacture example 2

[0305] Add p-hydroxybenzoic acid (994.5 g, 7.20 moles), terephthalic acid (299.0 g, 1.80 moles), isophthalic acid (299.0 g, 1.80 moles) and Formic acid (99.7g, 0.60 mol), 4,4'-dihydroxybiphenyl (446.9g, 2.40 mol) and acetic anhydride (1347.6g, 13.20 mol), after replacing the gas in the reactor with nitrogen, add 1- 0.18 g of methylimidazole was heated from room temperature to 150° C. over 30 minutes while stirring under a nitrogen stream, and refluxed at 150° C. for 1 hour.

[0306] Then, after adding 2.4 g of 1-methylimidazole, while distilling off by-produced acetic acid and unreacted acetic anhydride, the temperature was raised from 150° C. to 320° C. over 2 hours and 50 minutes. To complete the reaction, the contents were taken out from the reactor and cooled to room temperature to obtain a prepolymer (solid matter).

[0307] Then, the prepolymer was pulverized using a pulverizer, and the obtained pulverized product was heated from room temperature to 250° C. in a nitroge...

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Abstract

A liquid-crystal polyester resin composition including a liquid-crystal polyester and an amide compound that has the following structural units (I)-(III), a melting point of 100 DEG C or higher, and an area-average grain diameter of 5-50 [mu]m. The amide compound content is at least 0.005 part by mass and less than 0.1 part by mass per 100 parts by mass content of the liquid-crystal polyester. Structural unit (I): CH3-X-CO- (X represents a C10 or higher aliphatic hydrocarbon group or a hydroxyhydrocarbon group in which one or more hydrogen atoms of an aliphatic hydrocarbon group have been substituted by a hydroxy group.) Structural unit (II): -HN-Y-NH- (Y represents a C2 or higher hydrocarbon group.) Structural unit (III): -OC-Z-CO- (Z represents a C4 or higher aliphatic hydrocarbon group,alicyclic hydrocarbon group, or aromatic hydrocarbon group).

Description

technical field [0001] The invention relates to a liquid crystal polyester resin composition. [0002] This application claims priority based on Japanese Patent Application No. 2016-210790 filed in Japan on October 27, 2016, the contents of which are incorporated herein by reference. Background technique [0003] Liquid crystal polyesters are generally called molten liquid crystal type (thermotropic liquid crystal) polymers, have extremely excellent melt fluidity due to their specific behavior, and may have heat deformation resistance of 300° C. or higher depending on the structure. Taking advantage of such characteristics, liquid crystal polyesters are used in molded articles in OA including electronic parts, AV parts, heat-resistant tableware, and the like. [0004] As a molding method for obtaining the molded body, injection molding is generally used. In the injection molding method, a liquid crystal polyester resin composition obtained by mixing other components with l...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08L67/00B29B7/08B29C45/00C08K5/20
CPCC08K5/20C09K19/3838B29B7/002B29B7/90B29B7/726B29B7/286C08L67/03C08G63/605C08L77/02C08K3/346C08K7/14B29B9/12C08L77/06C08L67/02C08G63/6856C08J3/12B29B7/06B29C45/0001B29K2067/00B29K2105/0079C08L67/04C09K19/38
Inventor 胡新利原节幸
Owner SUMITOMO CHEM CO LTD