Catalyst system for rendering organic propellants hypergolic with hydrogen peroxide

• US 7,083,690 B2
• Filed: 06/26/2002
• Issued: 08/01/2006
• Est. Priority Date: 07/03/2001
• Status: Expired due to Fees

• Current Assignee: Wiley Organics Inc.
• Original Assignee: Wiley Organics Inc.
• Inventors: Wiley, David B., Dobbins, Thomas A.
• Primary Examiner(s): FELTON, AILEEN BAKER
• Application Number:
  US10/180,210
• Publication Number:
  US 20030015268A1
• Time in Patent Office: 1,497 Days
• Field of Search: 149/1, 149/108.6, 149/109.6, 602/11, 602/12
• US Class Current: 149/109.6
• CPC Class Codes: C06B 47/02 the components comprising a binary propellant
• CPC Class Codes: C06D 5/04 by auto-decomposition of single substances

Abstract

Novel catalysts capable of rendering both polar and non-polar organic fuels hypergolic with rocket-grade hydrogen peroxide are disclosed. These catalysts are complexes formed by reacting alkyl-substituted diamines or triamines, with metal salts of an aliphatic carboxylic acid or metal 1,3 dione chelates. In addition, the use of various acetylenic compounds as stability enhancing additives and/or promoters is described.

Claims

1. A method of rendering an organic fuel hypergolic with hydrogen peroxide, comprising the steps of:

providing a polar or non-polar organic fuel selected from the group consisting of kerosene, methanol, ethanol, isopropanol, octane, iso-octane, decane and mixtures thereof; and

contacting said organic fuel with a hypergolicity-imparting catalyst, thereby forming a catalyst-fuel mixture, wherein said hypergolicity-imparting catalyst comprises a complex of an alkyl-substituted diamine or alkyl-substituted triamine with a metal salt of an aliphatic carboxylic acid, wherein said metals are selected from the group consisting of manganese, cobalt, copper, silver, and combinations thereof and said metal salts of aliphatic carboxylic acids are selected from the group consisting of acetates, propionates, butyrates, and combinations thereof,

wherein the catalyst-fuel mixture is hypergolic with rocket grade hydrogen peroxide.

2. The method of claim 1 wherein said metal salt and said diamine or said triamine react in situ to form the hypergolicity-imparting catalyst.

3. The method of claim 1 wherein said hypergolicity-imparting catalyst is synthesized and isolated prior to contacting with said organic fuel.

4. The method of claim 1 wherein said amine comprises an alkyl substituted diamine.

5. The method of claim 4 wherein said alkyl substituted diamine is selected from the group consisting of 1,3-pentanediamine;

N,N-dimethylethylenediamine;

N,N,N′

,N′

-tetramethylenediamine and N,N,N′

,N′

-tetramethyl-1,3-butanediamine.

6. The method of claim 1 wherein said alkyl substituted triamine comprises N,N,N′

,N′

,N′

-pentamethyldiethylenetriamine.

7. The method of claim 1 wherein said hypergolicity-imparting composition further comprises a co-solvent or phase-joiner to impart solubility to said catalyst in non-polar organic fuels, said co-solvent or phase-joiner being selected from acetylenic compounds or a stoichiometric excess of said amine.

8. The method of claim 7 wherein said co-solvent or phase-joiner comprises a stoichiometric excess of N,N,N′

,N′

-tetramethylethylenediamine.

9. The method of claim 7 wherein said hypergolicity-imparting composition further comprises a terminal or internal acetylenic compound wherein said acetylenic compound renders said hypergolicity-imparting catalyst resistant to or impervious to the effects of auto-oxidation, thereby limiting the formation of insoluble precipitates, coagulates, or turbidity.

10. The method of claim 7 wherein said hypergolicity-imparting composition further comprises a conjugated acetylene.

11. The method of claim 10 wherein said conjugated acetylene comprises 1,4-dicyclopropylbuta-1,3-diyne.

12. The method of claim 1 wherein said catalyst fuel mixture is prepared under anaerobic conditions.

13. A method of rendering an organic fuel hypergolic with hydrogen peroxide, comprising the steps of:

providing a polar or non-polar organic fuel selected from the group consisting of kerosene, methanol, ethanol, isopropanol, octane, iso-octane, decane and mixtures thereof; and

contacting said organic fuel with a hypergolicity-imparting catalyst, thereby forming a catalyst-fuel mixture, wherein said hypergolicity-imparting catalyst comprises a complex of an amine selected from the group consisting of alkyl-substituted diamines and alkyl-substituted triamines with a metal salt of an aliphatic carboxylic acid, wherein said metals are selected from the group consisting of manganese, cobalt, copper, silver, and combinations thereof and said metal salts of aliphatic carboxylic acids are selected from the group consisting of acetates, propionates, butyrates, and combinations thereof,

the catalyst-fuel mixture comprising;

from about 50 to 97 weight % organic fuel;

from about 1 to 8 weight % metal salt of an aliphatic acid; and

from about 1 to 20 weight % amine,

wherein the catalyst-fuel mixture is hypergolic with rocket grade hydrogen peroxide.

14. The method of claim 13 wherein said hypergolicity-imparting composition further comprises a terminal or internal acetylenic compound having from 1 to 20 carbon atoms wherein said acetylenic compound renders said hypergolicity-imparting catalyst resistant to or impervious to the effects of auto-oxidation, thereby limiting the formation of insoluble precipitates, coagulates, or turbidity.