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

Halogen-free flame retardant resin composition and use thereof

A resin composition, flame retardant resin technology, applied in other household appliances, synthetic resin layered products, applications, etc., can solve the problem that the performance of resin cured products is difficult to further improve, and achieve low amine value, low activity, and improved Effect of Tg and Heat Resistance

Active Publication Date: 2014-07-16
GUANGDONG SHENGYI SCI TECH
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, this technical solution ignores the role of the auxiliary curing agent, making it difficult to further improve the performance of the resin cured product obtained by this solution.

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
  • Halogen-free flame retardant resin composition and use thereof
  • Halogen-free flame retardant resin composition and use thereof
  • Halogen-free flame retardant resin composition and use thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 13

[0099] A halogen-free flame-retardant resin composition, comprising:

[0100] (A) Phenoxyphosphazene compound (A 1 ) with compounds having a dihydrobenzoxazine ring (A 2 ) mixture: 45 parts by weight, phenoxyphosphazene compound (A 1 ) with compounds having a dihydrobenzoxazine ring (A 2 ) with a weight ratio of 1:25; (B) bisphenol A type epoxy resin with an epoxy equivalent of 1500: 45 parts by weight; (C) nitrogen-containing phenolic resin: 10 parts by weight, and (D) diaminodiphenyl Ether: 0.5 parts by weight.

[0101] A 1 The softening point (100~110°C) is a mixture of cyclic phenoxyphosphazene compounds and chain phenoxyphosphazene compounds shown in the following structural formula:

[0102]

[0103] m is an integer from 3 to 25; X is -N=P(OC 6 h 5 ) 3 ; Y is -P(OC 6 h 5 ) 4 ; n is an integer of 3-100.

[0104] A 2 Be the bisphenol A type benzoxazine resin described in following structural formula:

[0105]

[0106] R is -C(CH 3 ) 2 -, R 1 for

Embodiment 14

[0108] A halogen-free flame-retardant resin composition, comprising:

[0109] (A) Phenoxyphosphazene compound (A 1 ) with compounds having a dihydrobenzoxazine ring (A 2 ) mixture: 90 parts by weight, phenoxyphosphazene compound (A 1 ) with compounds having a dihydrobenzoxazine ring (A 2 ) in a weight ratio of 1:2; (B) bisphenol A type epoxy resin with an epoxy equivalent of 500: 30 parts by weight; (C) phenol novolac resin: 20 parts by weight, and (D) diaminodiphenyl sulfone : 10 parts by weight.

[0110] A 1 The softening point (100~110°C) is a mixture of cyclic phenoxyphosphazene compounds and chain phenoxyphosphazene compounds shown in the following structural formula:

[0111]

[0112] m is an integer from 3 to 25; X is -N=P(O)C 6 h 5 ; Y is -P(O)(C 6 h 5 ) 2 ; n is an integer of 3-100.

[0113] A 2 Be the bisphenol F type benzoxazine resin described in following structural formula:

[0114]

Embodiment 15

[0116] A halogen-free flame-retardant resin composition, comprising:

[0117] (A) Phenoxyphosphazene compound (A 1 ) with compounds having a dihydrobenzoxazine ring (A 2 ) mixture: 65 parts by weight, phenoxyphosphazene compound (A 1 ) with compounds having a dihydrobenzoxazine ring (A 2 ) in a weight ratio of 1:10; (B) bisphenol A type epoxy resin with an epoxy equivalent of 1000: 10 parts by weight; (C) bisphenol A type phenolic resin: 25 parts by weight, and (D) m-benzene Dimethylamine: 5 parts by weight.

[0118] A 1 The softening point (100~110°C) is a mixture of cyclic phenoxyphosphazene compounds and chain phenoxyphosphazene compounds shown in the following structural formula:

[0119]

[0120] m is an integer from 3 to 25; X is -N=P(OC 6 h 5 ) 3 ; Y is -P(OC 6 h 5 ) 4 ; n is an integer of 3-100.

[0121] A 2 It is a phenolphthalein type benzoxazine resin.

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

PropertyMeasurementUnit
softening pointaaaaaaaaaa
softening pointaaaaaaaaaa
softening pointaaaaaaaaaa
Login to View More

Abstract

Disclosed is a halogen-free flame-retardant resin composition. The resin composition comprises the following in parts by weight: (A) a mixture of a phenoxyphosphazene compound (A1) and a compound (A2) with a dihydrobenzoxazine ring: 45-90 parts by weight, the weight ratio of A1 to A2 being 1:25-1:2; (B) an epoxy resin with an epoxy equivalent of 500-2000: 10-45 parts by weight; (C) a phenolic resin: 10-25 parts by weight; and (D) an amine curing agent: 0.5-10 parts by weight. The pre-preg, laminated board and metal foil-coated laminated board for printed circuits prepared using the composition have the properties of high glass transition temperature (Tg), high heat resistance, low dielectric loss factor, low water absorption, low C.T.E and the like.

Description

technical field [0001] The present invention relates to a halogen-free flame-retardant resin composition and its application, specifically, the present invention relates to a halogen-free flame-retardant resin composition and prepregs, laminates and laminates for printed circuits made of it . Background technique [0002] In recent years, people's calls for environmentally friendly electronic products have become higher and higher, which has also made great progress in halogen-free technology. On the other hand, with the advent of the lead-free era, in addition to the halogen-free flame retardancy of printed circuit boards, the role of being able to cooperate with lead-free soft soldering electrodes has also become important. Therefore, laminated boards for printed circuits are also required to have higher heat resistance and reliability than before. At present, the main technologies are concentrated on phosphorus-modified epoxy resin and benzoxazine resin. It is well kno...

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): C08L63/00C08L63/02C08L61/06C08K13/02C08K5/5399C08K5/357C08K3/22C08K3/34C08K3/36C08G59/50B32B27/06B32B27/38B32B15/092H05K1/03
CPCH05K3/022C08K13/02C08G59/50C08K5/5399B32B15/092B32B27/06C08L63/00H05K1/0373H05K2201/0209H05K2201/012H05K1/0366C08L61/06C08K5/357B32B27/38C08J2361/06C08J2363/00B32B15/16B32B27/20B32B2260/025B32B2260/046B32B2264/102B32B2264/104B32B2307/306B32B2457/08C08G59/621C08J5/244C08J5/249C08L79/04C08L85/02C08L71/00H05K1/0353
Inventor 何岳山苏世国
Owner GUANGDONG SHENGYI SCI TECH
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