Aromatic hydrocarbon formaldehyde resin, modified aromatic hydrocarbon formaldehyde resin and epoxy resin, and method for producing these

Patent metadata

Field	Value
Publication number	US-9725551-B2
Application number	US-201414896487-A
Country	US
Kind code	B2
Filing date	Jun 16, 2014
Priority date	Jun 18, 2013
Publication date	Aug 8, 2017
Grant date	Aug 8, 2017

Abstract

There is provided an aromatic hydrocarbon formaldehyde resin obtained by reacting an aromatic hydrocarbon compound (A) represented by the following formula (1) with formaldehyde (B) in the presence of an acidic catalyst.

wherein R represents an organic group having 1 to 10 carbon atoms; l represents an integer of 0 to 2, and m and n represent integers satisfying 1≦m+n≦10, m≧0 and n≧1.

First claim

The invention claimed is:

1. An aromatic hydrocarbon formaldehyde resin, being obtained by reacting an aromatic hydrocarbon compound (A) represented by the following formula (1) with formaldehyde (B) in the presence of an acidic catalyst:

wherein R represents an organic group having 1 to 10 carbon atoms; 1 represents an integer of 0 to 2, and m and n represent integers satisfying 1≦m+n≦10, m≧0 and n≧1, said aromatic hydrocarbon formaldehyde resin comprising substantially no diarylmethane.

2. The aromatic hydrocarbon formaldehyde resin according to claim 1 , being obtained by reacting the aromatic hydrocarbon compound (A) with formaldehyde (B) in a molar ratio of (A):(B)=1:1 to 1:20 in the presence of an acidic catalyst.

3. The aromatic hydrocarbon formaldehyde resin according to claim 1 , wherein the reaction of the aromatic hydrocarbon compound (A) with formaldehyde (B) is carried out in the presence of an alcohol.

4. The aromatic hydrocarbon formaldehyde resin according to claim 1 , having a weight-average molecular weight of 200 to 25,000.

5. The aromatic hydrocarbon formaldehyde resin according to claim 1 , having an oxygen content of 7 to 18% by mass.

6. A method for producing an aromatic hydrocarbon formaldehyde resin, comprising reacting an aromatic hydrocarbon compound (A) represented by the following formula (1) with formaldehyde (B) in the presence of an acidic catalyst:

wherein R represents an organic group having 1 to 10 carbon atoms; 1 represents an integer of 0 to 2, and m and n represent integers satisfying 1≦m+n≦10, m≧0 and n≧1 to produce an aromatic hydrocarbon formaldehyde resin comprising substantially no diarylmethane.

7. A modified aromatic hydrocarbon formaldehyde resin, being obtained by reacting an aromatic hydrocarbon formaldehyde resin according to claim 1 with at least one selected from the group consisting of compounds represented by the following formulae (2) and (3) in the presence of an acidic catalyst:

wherein X and Y each independently represent a hydrogen atom or an organic group having 1 to 10 carbon atoms; and a and b represent integers satisfying 1≦a+b≦10, a≧1 and b≧0, and c represents an integer of 0 to 2.

8. The modified aromatic hydrocarbon formaldehyde resin according to claim 7 , wherein the compounds represented by the formulae (2) and (3) are at least one selected from the group consisting of phenol, cresol, catechol, hydroquinone, phenylphenol, biphenol, naphthol, dihydroxynaphthalene, hydroxyanthracene and dihydroxyanthracene.

9. A method for producing a modified aromatic hydrocarbon formaldehyde resin, comprising reacting an aromatic hydrocarbon formaldehyde resin according to claim 1 with at least one selected from the group consisting of compounds represented by the following formulae (2) and (3) in the presence of an acidic catalyst:

wherein X and Y each independently represent a hydrogen atom or an organic group having 1 to 10 carbon atoms; and a and b represent integers satisfying 1≦a+b≦10, a≧1 and b≧0, and c represents an integer of 0 to 2.

10. An epoxy resin, being obtained by reacting a modified aromatic hydrocarbon formaldehyde resin according to claim 7 with epichlorohydrin.

11. A method for producing an epoxy resin, comprising reacting a modified aromatic hydrocarbon formaldehyde resin according to claim 7 with epichlorohydrin to thereby obtain the epoxy resin.

12. The aromatic hydrocarbon formaldehyde resin according to claim 2 , wherein the reaction of the aromatic hydrocarbon compound (A) with formaldehyde (B) is carried out in the presence of an alcohol.

13. The aromatic hydrocarbon formaldehyde resin according to claim 2 , having a weight-average molecular weight of 200 to 25,000.

14. The aromatic hydrocarbon formaldehyde resin according to claim 2 , having an oxygen content of 7 to 18% by mass.

15. The aromatic hydrocarbon formaldehyde resin according to claim 2 , comprising substantially no diarylmethane.

16. A modified aromatic hydrocarbon formaldehyde resin, being obtained by reacting an aromatic hydrocarbon formaldehyde resin according to claim 2 with at least one selected from the group consisting of compounds represented by the following formulae (2) and (3) in the presence of an acidic catalyst:

wherein X and Y each independently represent a hydrogen atom or an organic group having 1 to 10 carbon atoms; and a and b represent integers satisfying 1≦a+b≦10, a≧1 and b≧0, and c represents an integer of 0 to 2.

17. The aromatic hydrocarbon formaldehyde resin according to claim 2 , having a weight-average molecular weight of 200 to 25,000.

18. The aromatic hydrocarbon formaldehyde resin according to claim 2 , having an oxygen content of 7 to 18% by mass.

19. The aromatic hydrocarbon formaldehyde resin according to claim 2 , comprising substantially no diarylmethane.

Assignees

• Mitsubishi Gas Chemical Co

Inventors

• Higashihara Go
• Okoshi Atsushi

Classifications

• C08G14/12

  Chemically modified polycondensates · CPC title

• C08L63/00

  Compositions of epoxy resins; Compositions of derivatives of epoxy resins · CPC title

• C08G4/00 Primary

  Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O— (of cyclic oligomers of aldehydes C08G2/00) · CPC title

• C08G2/26

  with compounds containing carbon-to-carbon unsaturation · CPC title

• C08G10/04 Primary

  Chemically-modified polycondensates · CPC title