US Patent 4,293,314:
Gelled Fuel-Air Explosive
United States Patent [19]
Stull
[11] 4,293,314
[45] Oct. 6, 1981
[54] GELLED FUEL-AIR EXPLOSIVE METHOD
[75] Inventor: Bertram O. Stull, Ridgecrest, Calif.
[73] Assignee: The United States of America as represented by the Secretary of the Navy, Washington, D.C.
[21] Appl. No.: 111,453
[22] Filed: Jan. 11, 1980
- [51] Int. Cl.3
C10L 7/00
- [52] U.S. Cl.
44/7 A; 44/7 R;
44/7 D; 102/90; 102/363
- [58] Field of Search
102/90; 44/7 R, 7 E, 44/7 D, 7 A
[56] References Cited
U.S. PATENT DOCUMENTS
- 3,539,311 11/1970 Cohen et al.
44/7 A
- 3,634,157 1/1972 Batson
44/7 E
- 3,685,453 8/1972 Hawrick
102/90
- 3,730,093 5/1973 Cummings
102/90
- 3,795,556 3/1974 Sippel et al.
44/7 E
- 3,955,509 3/1976 Carlsen
102/90
- 3,994,696 11/1976 Adicoff
44/7 A
- 4,157,928 6/1979 Falterman et al.
102/90
Primary Examiner—Edward A. Miller
Attorney, Agent, or Firm—R. S. Sciascia; W. Thom Skeer; Lloyd E. K. Pohl
[57] ABSTRACT
1,2-Butylene oxide as a fuel for a fuel air explosive weapon. The oxide may be used either as a pure liquid or gelled with a gelling agent such as silicon dioxide, particulate carbon or aluminum octoate.
3 Claims, No Drawings
GELLED FUEL-AIR EXPLOSIVE METHOD
BACKGROUND OF THE INVENTION
1. Field of the Invention 5
This invention relates to fuels for fuel air explosive weapons. More particularly, this invention relates to a method for causing an explosion comprising the steps of dispersing a cloud of liquid fuel in the air and detonating the cloud wherein the cloud is composed of particles of 10 gelled or ungelled 1,2-butylene oxide.
1. Description of the Prior Art
Fuel air explosive weapons are now well known. A typical example of one is depicted in U.S. Pat. No. 3,955,509 which was issued to Gary A. Carlson on May 15 11, 1976.
Fuel air explosive weapons may be described as devices which, upon activation, cause liquid fuel particles to be dispersed in the form of a detonable cloud in the air and then detonate the cloud. 20
A number of fuels have been used in fuel air explosive weapons. Among these are ethylene oxide and propylene oxide. Because of the ease with which is cloud of ethylene oxide or propylene oxide can be detonated, these two materials are the most commonly used. However, 25 these fuels have certain drawbacks.
One drawback, common to both ethylene oxide and propylene oxide, is toxicity. Both materials are highly toxic. A concentration of 50 parts per million of ethylene 30 oxide in the air may have harmful effects on one breathing the air for about 8 hours. Propylene oxide is less toxic than ethylene oxide but is still highly toxic. A concentration of 100 parts per million of propylene oxide breathed for about 8 hours may have undesirable 35 effects. Naturally, when fuel air explosive devices are stored in a confined area such as aboard a ship, exposure for 8 hours is not unusual.
Another drawback common to ethylene oxide and propylene oxide is the fact that both have relatively low 40 boiling points, 10.4° C. and 34.2° C. respectively. This makes the two difficult to handle in loading operations. High vapor pressures also contribute to difficulty in handling.
A drawback particularly associated with ethylene 45 oxide is its tendency to polymerize during storage. Left alone in a fuel air explosive weapon or other container, ethylene oxide tends to self polymerize. The polymerized material is unsuitable for use as a fuel for a fuel air explosive device. Unpolymerized ethylene oxide, on the 50 other hand is highly desirable as a fuel insofar as detonability is concerned. Clouds containing from as little as 3 up to as much as 100 percent by volume of ethylene oxide are detonable. The detonation limits of propylene oxide, on the other hand, range from about 3.1 to about 55 27.5 percent by volume.