Halogen-free, nonflammable and high glass transition temperature phenolic resin-based curing agent and process for producing the same

Patent metadata

Field	Value
Publication number	US-9512257-B2
Application number	US-201414223300-A
Country	US
Kind code	B2
Filing date	Mar 24, 2014
Priority date	Mar 28, 2013
Publication date	Dec 6, 2016
Grant date	Dec 6, 2016

Abstract

A phenolic-type phosphorous curing agent works by grafting a phosphorous compound onto a benzene ring to substitute hydrogen atoms and is halogen-free and nonflammable; when acting with and curing an epoxy resin, the curing agent helps to form a higher crosslink density and excellent heat tolerance to let the epoxy resin suitable for use in making PCB's insulating layer or semiconductor packaging as well as to endow the PCB's insulating layer or semiconductor packaging provided with excellent flame retardance and high glass transition temperature (Tg).

First claim

What is claimed is:

1. A phenolic-type phosphorous curing agent, having a molecular weight ranging between 550 and 12000, having a phosphorus content ranged between 3.74% and 9.06%, being halogen-free and nonflammable, and having a chemical structure described as chemical structure formulas (I), (II), (III), (IV) or (V):

X═H; n is a positive integer greater than zero, and has a value determined by the molecular weight;

where, X═H; n is a positive integer greater than zero, and has a value determined by the molecular weight;

where, X═H; n is a positive integer greater than zero, and has a value determined by the molecular weight;

where, X═H; n is a positive integer greater than zero, and has a value determined by the molecular weight;
and G in the above chemical structures (I)-(V) is G 1 or G 2 :

2. A process for producing the phenolic-type phosphorous curing agent of claim 1 , including:
a) selecting ODOPM or DOPO-HQ as a phosphorous-containing compound;
b) in the presence of a catalyst and a water-carrying agent, conducting a dehydrating reaction by reacting a phenolic resin having a molecular-weight ranged between 350 and 4,000 with the phosphorous-containing compound of step a) in a relative equivalence ratio of 1:0.4 to 1:2 to obtain the phenolic-type phosphorous curing agent;
wherein the catalyst is added in the amount of 3-5%, by weight of the total weight of the phosphorous-containing compound and the phenolic resin of step b);
wherein the water-carrying agent is added in the amount of 10-15%, by weight of the total weight of the phosphorous-containing compound and the phenolic resin of step b), and
wherein the water-carrying agent is at least one selected from the group consisting of benzene, toluene, xylene, butanone, methyl isobutyl ketone, cyclohexanone and cyclohexanol.

3. The process for producing phenolic-type phosphorous curing agent defined in claim 2 , wherein the phenolic resin is at least one selected from the group consisting of BPA-type phenolic resin, salicylaldehyde-type phenolic resin, glyoxal-type phenolic resin, hydroquinone-type phenolic resin and benzaldehyde-type phenolic resin.

4. The process for producing phenolic-type phosphorous curing agent defined in claim 2 , wherein at step b) the phenolic resin and the phosphorous-containing compound is reacted in a relative equivalence ratio of 1:0.6 to 1:1.5.

5. The process for producing phenolic-type phosphorous curing agent defined in claim 3 , wherein a molecular weight of the phenolic resin is ranged between 1,000 and 3,000.

6. The process for producing the phenolic-type phosphorous curing agent of claim 2 , wherein the catalyst of step b) is at least one selected from the group consisting of sulfuric acid, methanesulfonic acid, trifluoromethanesulfonic acid, p-toluene sulphonic acid, sodium acetate, potassium acetate, cobalt acetate, ferric acetate, zinc acetate and lead acetate.

Assignees

• Nanya Plastics Corp

Inventors

• Fung Dein-Run
• Liao Te-Chao
• Chao Chia-Cheng
• Chen hao-sheng

Classifications

• C08G59/621

  Phenols · CPC title

• C08G8/04

  of aldehydes · CPC title

• C08G8/08

  of formaldehyde, e.g. of formaldehyde formed in situ · CPC title

• C08G8/28 Primary

  Chemically modified polycondensates · CPC title