Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Curable resin composition and cured products thereof

A technology of curable resin and composition, applied in the field of liquid curable resin composition, to achieve the effects of excellent low coloring, excellent refractive index, and excellent storage stability

Active Publication Date: 2013-12-25
ADEKA CORP
View PDF21 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the compounds described in these documents have problems of storage stability due to crystallization in the resin composition and colorability of the obtained cured product.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Curable resin composition and cured products thereof
  • Curable resin composition and cured products thereof
  • Curable resin composition and cured products thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1-1~1-4

[0109][Examples 1-1 to 1-4 and Comparative Examples 1-1 to 1-3] Production of curable resin compositions No.1 to No.4 and comparative curable resin compositions No.1 to No.3

[0110] According to Table 1, heat the following (1-1) to (1-3) epoxy compounds and (2) diluent to 80°C to dissolve them, then cool down to 60°C, add (3-1) and (3-2 ) The energy ray-sensitive cationic polymerization initiator was completely dissolved to prepare curable resin compositions No. 1 to No. 4 and comparative curable resin compositions No. 1 to No. 3, respectively.

[0111] [complex]

[0112] (1-1) 1,1-bis(4-(2,3-epoxypropoxy)phenyl)-3-phenylindane (corresponding to the compound when n=0 of the above-mentioned compound No.40 ), hereinafter referred to as epoxy compound No.1.

[0113] Epoxy compound No.1

[0114] (1-2) 1,1-bis(4-(2,3-epoxypropoxy)phenyl)-3,5-diphenylindane (equivalent to n=0 of the above compound No.31 When the compound), hereinafter referred to as epoxy compound No.2.

[0...

Embodiment 2-1~2-4 and comparative example 2-1 and 2-2

[0133] [Examples 2-1 to 2-4 and Comparative Examples 2-1 and 2-2] Production of Cured Products No.1 to No.4 and Comparative Cured Products No.2 and No.3

[0134] The curable resin compositions and comparative curable resin compositions obtained in Examples 1-1 to 1-4 and Comparative Examples 1-2 and 1-3 were heated to 60°C, respectively, and coated on the mold release treatment. on a glass substrate. Together with a 1.00mm spacer, use a piece of glass to clamp and paste, and use a high-pressure mercury lamp to 3000mJ / cm 2 (total 6000mJ / cm 2 ) After exposing one side of the glass, it was treated at 150° C. for 2 hours to be cured. After cooling to room temperature, the cured product was peeled off from the glass to prepare cured product No.1 to No.4 and comparative cured product No.2 and No.3.

[0135] [Examples 3-1 to 3-4 and Comparative Examples 3-1 and 3-2] Evaluation of Cured Products No.1 to No.4 and Comparative Cured Products No.2 and No.3

[0136] The "refractive ind...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

A curable resin composition which comprises both an epoxy compound represented by general formula (I) and an energy -ray-sensitive cationic-polymerization initiator. In general formula (I), X, Y and Z are each a C1-10 alkyl group which may be substituted with a halogen atom, a C6-20 aryl group, a C6-20 aryloxy group, a C6-20 arylthio group, a C8-20 arylalkenyl group, a C7-20 arylalkyl group, a C2-20 heterocyclic group, or a halogen atom; k is a number of 0 to 4; p is a number of 0 to 8; r is a number of 0 to 4; n is 0 to 10; x is a number of 0 to 4, and y is a number of 0 to 4, with the sum of x and y being 2 to 4; and when n is not 0, the epoxy compound can take the form of any optical isomer.

Description

technical field [0001] The present invention relates to a liquid curable resin composition which is suitable for producing cured products of high refractive index resins, has excellent handling properties, and has little coloration after curing. Background technique [0002] Epoxy resins (compounds) have been actively developed in the fields of electronic materials and optical materials due to their excellent electrical properties, heat resistance, and adhesive properties of cured resins obtained by combining them with curing agents. . For example, in the field of electronic materials, semiconductor sealing materials, etc. are mentioned, and in the field of optical materials, antireflection films such as liquid crystal displays, protective films of color filters, optical waveguides, and optical devices such as cameras are used. Lenses, mirrors and prisms etc. In particular, a high refractive index is required for the purpose of weight reduction in optical material applicat...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08G59/24
CPCC08G59/24
Inventor 高日俊辅五十岚浩之佐藤直美后藤雅治
Owner ADEKA CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products