Trifunctional benzoxazine

Patent metadata

Field	Value
Publication number	US-9714322-B2
Application number	US-201514980407-A
Country	US
Kind code	B2
Filing date	Dec 28, 2015
Priority date	Dec 29, 2014
Publication date	Jul 25, 2017
Grant date	Jul 25, 2017

Abstract

A meta-substituted trifunctional benzoxazine monomer and compositions containing the same, wherein the trifunctional benzoxazine monomer is represented by the following structure:

First claim

What is claimed is:

1. A meta-substituted trifunctional benzoxazine monomer represented by the following structure (A):

and having a molecular weight (MVV) of about 699 as determined by Liquid Chromatography Mass Spectrometry (LCMS).

2. A reaction product composition obtained by reacting 1,1,1-tris(4-hydroxyphenyl)ethane with m-toluidine and methyl formcel, wherein the composition comprises a meta-substituted trifunctional benzoxazine represented by structure (A) as a major component, and benzoxazines represented by structures (B) and (C) as minor components:

and wherein the molecular weight of structure (A), (B) and (C) is 699, 687 and 568, respectively, as determined by Liquid Chromatography Mass Spectrometry (LCMS).

3. The reaction product composition of claim 2 , wherein the stoichiometry for reacting 1,1,1-tris(4-hydroxyphenyl)ethane with m-toluidine and methyl formcel is as follows: for each mole of m-toluidine, 0.25-0.5 mole of 1,1,1-tris(4-hydroxyphenyl)ethane, and 1.5-20 moles of methyl formcel.

4. A reaction product composition obtained by preparing a reaction mixture comprising ,1,1-tris(4-hydroxyphenyl)ethane, m-toluidine, and paraformaldehyde; and heating the reaction mixture to a temperature at which chemical reaction occurs, wherein the composition comprises, as a major component, a meta-substituted trifunctional benzoxazine monomer represented by the following structure (A):

said trifunctional benzoxazine monomer having a molecular weight (MVV) of 699 as determined by Liquid Chromatography Mass Spectrometry (LCMS).

5. A resin composition comprising the meta-substituted trifunctional benzoxazine monomer of claim 1 and another benzoxazine monomer.

6. A resin composition comprising the reaction product of claim 1 and a thermosettable resin.

7. A curable composition comprising:
the meta-substituted trifunctional benzoxazine monomer of claim 1 and at least one thermosettable resin component selected from the group consisting of: monofunctional benzoxazines; multifunctional benzoxazines other than said substituted trifunctional benzoxazine monomer; epoxy resins, bismaleimide (BMI), phenolic resins, formaldehyde-phenol, cyanate ester, unsaturated polyester, and combinations thereof.

8. A curable composition comprising:
the reaction product composition of claim 2 and at least one thermosettable resin component selected from the group consisting of: monofunctional benzoxazines; multifunctional benzoxazines other than said substituted trifunctional benzoxazine monomer; epoxy resins, bismaleimide (BMI), phenolic resins, formaldehyde-phenol, cyanate ester, unsaturated polyester, and combinations thereof.

9. A resin composition comprising:
the meta-substituted trifunctional benzoxazine monomer of claim 1 ; and
a catalyst selected from the group consisting of: boron trifluorodietherate (BF 3 O(Et) 2 ); phosphorous pentachloride (PCl 5 ); phosphorous trichloride (PCl 3 ); phosphorus oxychloride (POCl 3 ); titanium chloride (TiCl 4 ); aluminum chloride (AlCl 3 ); antimony pentachloride (SbCl 5 ); thiodiphenol; 2,4-di-tert-butylphenol; methyl tosylate; methyl triflate (MeOTf); cyanate esters; 2-ethyl-4-methylimidazole(EMI); alkylenic acids; adipic acid; p-toluenesulfonic acid; and combinations thereof.

10. The resin composition of claim 5 further comprising a catalyst selected from the group consisting of:
boron trifluorodietherate (BF 3 O(Et) 2 ), phosphorous pentachloride (PCl 5 ), phosphorous trichloride (PCl 3 ), phosphorus oxychloride (POCl 3 ), titanium chloride (TiCl 4 ), aluminum chloride (AlCl 3 ), antimony pentachloride (SbCl 5 ); thiodiphenol; 2 , 4 -di-tert-butylphenol; methyl tosylate; methyl triflate (MeOTf); cyanate esters; 2-ethyl-4-methylimidazole (EMI); alkylenic acids; adipic acid; p-toluenesulfonic acid; and combinations thereof.

11. A composite material comprising reinforcement fibers and a curable matrix resin,
wherein the curable matrix resin comprises the meta-substituted trifunctional benzoxazine monomer of claim 1 .

12. A composite material comprising reinforcement fibers and a curable matrix resin,
wherein the curable matrix resin comprises the reaction product composition of claim 2 .

13. A prepreg comprising a layer of reinforcement fibers impregnated with or embedded in a curable matrix resin comprising the meta-substituted trifunctional benzoxazine monomer of claim 1 .

14. The prepreg of claim 13 , wherein the reinforcement fibers are in the form of continuous, unidirectionally aligned fibers or woven fabric.

15. The composite materials of claim 11 , wherein the reinforcement fibers are selected from carbon fibers, glass fibers, aramid fibers, and combination thereof.

16. A composite structure manufactured by combining reinforcement fibers with the resin composition of claim 5 .

17. A composite structure manufactured by combining reinforcement fibers with the resin composition of claim 6 .

18. A composite structure manufactured by impregnating or infusing reinforcement fibers with the curable composition of claim 7 , followed by curing.

Assignees

• Cytec Ind Inc

Inventors

• Gupta Ram B
• Cross Paul Mark

Classifications

• C08J2379/02

  Polyamines · CPC title

• C08L79/02

  Polyamines · CPC title

• C08G73/0233 Primary

  Polyamines derived from (poly)oxazolines, (poly)oxazines or having pendant acyl groups · CPC title

• C08J2463/00

  Characterised by the use of epoxy resins; Derivatives of epoxy resins · CPC title

• C07D265/16 Primary

  with only hydrogen or carbon atoms directly attached in positions 2 and 4 · CPC title