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Methacrylic resin composition and molded body

A methacrylic, resin composition technology, applied in optics, instruments, optical components, etc., can solve the problems of poor molding processability, operability, productivity, weak strength, foaming, etc., and achieves excellent appearance, molding and processing. Excellent effect

Active Publication Date: 2021-06-18
ASAHI KASEI KK
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, the above-mentioned acrylic resin with improved heat resistance (heat-resistant acrylic resin) has a disadvantage of being easily thermally decomposed during high-temperature molding compared with a copolymer of methyl methacrylate and acrylate, which is a general-purpose acrylic resin.
[0006] In addition, with the increase in size and thickness of molded products (filming, etc.), molding at high temperatures and residence time at high temperatures become longer, so there is a disadvantage that foaming may occur during molding processing.
[0007] Furthermore, since the heat-resistant acrylic resin is weak in strength and low in toughness, there is a problem that the moldability and workability of the film deteriorate in productivity.

Method used

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  • Methacrylic resin composition and molded body
  • Methacrylic resin composition and molded body
  • Methacrylic resin composition and molded body

Examples

Experimental program
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Effect test

Embodiment

[0571] Hereinafter, specific examples and comparative examples are given and described, but the present invention is not limited to these examples.

[0572] [raw material]

[0573] The raw materials used in the following examples and comparative examples are as follows.

[0574] [[Monomers constituting methacrylic resin]]

[0575] ・Methyl methacrylate (MMA): manufactured by Asahi Kasei Chemical Co., Ltd. (as a polymerization inhibitor, 2,4-dimethylformamide manufactured by Chugai Trading Co., Ltd. was added at 2.5 ppm) -6-tert-butylphenol (2,4-di-methyl-6-tert-butylphenol)).

[0576] · N-phenylmaleimide (N-PMI): manufactured by Nippon Shokubai Co., Ltd.

[0577] · N-cyclohexylmaleimide (N-CMI): manufactured by Nippon Shokubai Co., Ltd.

[0578] - Methyl 2-(hydroxymethyl)acrylate (MHMA): manufactured by Combi Bloks.

[0579] ·Acrylonitrile (AN)

[0580] [[Organic solvents]]

[0581] - m-xylene: manufactured by Mitsui Chemicals, Ltd.

[0582] ·Toluene

[0583] [[other]]...

manufacture example 1

[0763] In a 1.25m tank equipped with a stirring device with paddle-shaped wings, a temperature sensor, a cooling pipe, and a nitrogen introduction pipe 3 In the reactor, add 432.3kg of methyl methacrylate (MMA), 33.0kg of N-phenylmaleimide (N-PMI), 84.7kg of N-cyclohexylmaleimide (N -CMI), 450.0kg of m-xylene, and 0.28kg of n-octylmercaptan were dissolved to prepare a raw material solution. While blowing nitrogen therein, the temperature was raised to 125°C while stirring.

[0764] Separately, an initiator supply solution obtained by mixing 0.23 kg of Perhexa C-75 and 1.82 kg of m-xylene was prepared.

[0765] When the raw material solution reached 127°C, the supply (addition) of the initiator supply solution (polymerization initiator mixed solution) was started according to the procedures (1) to (6).

[0766] (1) 0.0 to 0.5 hours: the supply rate is 1.00 kg / hour.

[0767] (2) 0.5 to 1.0 hours: the supply rate is 0.50 kg / hour.

[0768] (3) 1.0 to 2.0 hours: the supply rate...

manufacture example 2

[0779] Assuming 380.1kg of methyl methacrylate (MMA), 6.1kg of N-phenylmaleimide (N-PMI), 163.9kg of N-cyclohexylmaleimide (N-CMI), 450 kg of meta-xylene and 0.110 kg of n-octyl mercaptan were carried out in the same manner as in Production Example 1.

[0780] The glass transition temperature of the obtained particles was 145°C.

[0781] In addition, the composition determined by NMR was MMA unit: 71 mass%, N-PMI unit: 1 mass%, N-CMI unit: 28 mass%.

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Abstract

An object of the present invention is to provide a methacrylic resin composition which has sufficient optical properties for practical use and is excellent in heat resistance, thermal stability, and molding processability, and a molded article containing the same. The methacrylic resin composition of the present invention is characterized in that it contains methacrylate monomer units (A): 50 to 97% by mass, and structural units (B) having a ring structure in the main chain: 3 to 30% by mass %, Other vinyl-based monomer units (C) that can be copolymerized with methacrylate monomers: 0 to 20% by mass, methacrylic resins meet specific conditions, and are heated at 280°C in a nitrogen environment The weight average molecular weight residual rate after 1 hour is 80% or more, and the weight average molecular weight residual rate after heating at 280° C. in air for 0.5 hour is 80% or more.

Description

technical field [0001] The present invention relates to an improved methacrylic resin composition and a molded article containing the methacrylic resin composition. Background technique [0002] In recent years, with the expansion of the display market, there has been an increasing demand for clearer viewing of images, and optical materials that impart higher optical characteristics in addition to transparency, heat resistance, and strength are required. [0003] Acrylic resins ((meth)acrylate polymers) have attracted attention as the aforementioned optical materials from the viewpoint of transparency, surface hardness, optical properties, and the like. [0004] Conventionally, it has been reported that, among acrylic resins, especially by copolymerizing glutaric anhydride (for example, see Patent Document 1), maleic anhydride (for example, see Patent Document 2) and the like with (meth)acrylate monomers, it has been reported that Acrylic resins with improved heat resistanc...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F220/18C08J5/00C08J5/18C08K5/13C08K5/36C08K5/49C08L33/10
CPCC08J5/18C08K5/13C08K5/36C08K5/49C08F220/14C08J2333/12C08F220/1804C08F222/402C08L33/12C08K5/526C08K5/372C08K5/3477C08K5/134C08K5/3492C08F222/40C08L33/10G02B1/04C08F220/18C08F212/08C08F220/44C08F136/06C08K5/005C08K5/0025B29C48/022B29K2833/08B29K2833/12C08F2500/01C08F2500/03C08J2333/08C08J2333/10C08F220/42C08F220/04
Inventor 平本千寻村上史树
Owner ASAHI KASEI KK