WO1997049274A2 - A method for generating nuclear fusion through high pressure - Google Patents

A method for generating nuclear fusion through high pressure Download PDF

Info

Publication number
WO1997049274A2
WO1997049274A2 PCT/US1997/010012 US9710012W WO9749274A2 WO 1997049274 A2 WO1997049274 A2 WO 1997049274A2 US 9710012 W US9710012 W US 9710012W WO 9749274 A2 WO9749274 A2 WO 9749274A2
Authority
WO
WIPO (PCT)
Prior art keywords
bubbles
gas
bubble
pressure
liquid
Prior art date
Application number
PCT/US1997/010012
Other languages
French (fr)
Inventor
Shui-Yin Lo
Original Assignee
American Technologies Group, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by American Technologies Group, Inc. filed Critical American Technologies Group, Inc.
Priority to AU33842/97A priority Critical patent/AU3384297A/en
Publication of WO1997049274A2 publication Critical patent/WO1997049274A2/en

Links

Classifications

    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21BFUSION REACTORS
    • G21B3/00Low temperature nuclear fusion reactors, e.g. alleged cold fusion reactors
    • G21B3/008Fusion by pressure waves
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/10Nuclear fusion reactors

Definitions

  • the present invention describes a viable and effective means to change the structure of materials for the creation of viable micro-thermonuclear fusion, created through the energy of collapsing bubbles.
  • the present invention investigates the creation of extremely high pressure inside a bubble, not by shock wave alone but by the creation of high pressure due to expansion from rapid heating followed by collapsing due to conduction of heat to the surrounding liquid. While prior methods for which Moss and Wu investigate a curiosity, the current invention is directed towards a commercial method to generate the requisite high pressure needed to generate nuclear fusion as well as a method to generate materials such as metallic hydrogen industrial diamonds and nuclear fusion heat energy.
  • the present invention heats up the entire core of the collapsed bubble, instead of just at the shock front, as in Moss et al. Energy gains are calculated to exceed 1000:1 for the present invention, making it a commercially viable method for generating nuclear fusion power.
  • the pressure from collapsing bubbles can generate sufficient energy to create nuclear energy fusion heat, to generate metallic hydrogen and to generate high- intensity x-rays, produce industrial grade diamonds. While all of the above and many more products can be achieved utilizing the energy of a collapsing bubble, the production of such products have been more of an academic or laboratory curiosity, than a valuable commercial method to generate sufficient quantity of collapsing bubbles for producing commercial quantities of resultant products.
  • the current invention is directed towards a commercially viable product where the output exceeds the costs of input to generate commercial viable quantities of nuclear fusion energy, diamonds, metals and x-rays.
  • the present invention as applied to the creation of nuclear fusion heat energy conditions in a bubble of deuterium and oxygen in heavy water will generate sufficient energy that far exceeds the input energy.
  • the method involves the creation of bubbles of deuterium and oxygen gas and injecting these bubbles into heavy water, filling a chamber with said deuterium and said oxygen in the heavy water.
  • a vacuum is pulled on the heavy water in the chamber, to generate first the bubbles and then to cause expansion of the bubbles from 10 microns to 100 microns.
  • An external pressure is then applied to the heavy water and subsequently transmitted to the bubbles.
  • the bubbles collapse due to the externally applied pressure. Heating and subsequent expansion of these bubbles at 10 microns is achieved by a laser, which is used to ignite the bubble contents by selecting the correct absorption frequency, thereby imparting symmetry to the bubbles.
  • the present invention can also be applied to the creation of commercially viable new materials such as diamond, high-intensity x-rays and metallic hydrogen under extremely high pressure.
  • the present invention when utilized with superfliud helium as a media can be used as a method of accelerating particles.
  • FIG 1 Illustrates an apparatus to practice the method of the invention.
  • Figure 2 illustrates a bubble of deuterium and oxygen in heavy water.
  • Figure 3 illustrates bubbles of deuterium and oxygen formed around I E crystals in heavy water.
  • Figure 4 illustrates the expansion of bubbles due to vacuum.
  • Figure 5 illustrates application of external pressure to compress the radius of the bubbles.
  • Figure 6 illustrates laser ignition to impart symmetry to the bubbles.
  • Figure 7 illustrates the compression of the symmetrical bubble to 1 micron. microns as illustrated in exploded view Figure 4. The precise type of value is not critical.
  • External pressure (127) is applied by switching on the electro-magnetic plungers (125) of Figure 2 in a controlled manner, the optimum external pressure as a function of time is described in mathematical formulas that are set forth herein and below.
  • the bubbles (121) contract from the 100 micron to about a 10 micron size as illustrated in exploded view Figure 5 by external pressure (122). Ignition of the deuterium-oxygen gas mixture (122) inside each bubble (121) is done by a laser with the right absorption frequency either for deuterium gas or oxygen gas.
  • the external applied heat (131) from the laser (160) in Figure 1 will cause combustion of the deuterium and oxygen gas to heavy water vapor (135) not shown.
  • the heat from the heavy water vapor (135) will be conducted away by the surrounding heavy water (101).
  • the cooling of the heavy water vapor (135) inside the bubble (121) will cause the vapor (135) to condense on the surface of the bubble (121), creating a low pressure inside the bubble (121) with very little matter.
  • the following is a preferred embodiment for the creation of extreme high pressure. Creation of a mixture of deuterium gas and oxygen gas at the ration of 2:1.
  • the known electrolysis process is applied to heavy water with DC voltage and two electrodes. Heavy water disassociates into deuterium gas and oxygen gas in the cathode and anode respectively, in exactly the ratio of 2:1. They are then gently mixed together to avoid explosion. The exact ratio is important so that when deuterium gas and oxygen gas combust to from heavy water, there is no residual gas.
  • deuterium gas (102) and oxygen gas (103) in heavy water(l ⁇ l) under pressure as set forth in exploded view Figure 2.
  • the introduction can be by mixing, dissolving any way to introduce the mixture in heavy water.
  • structured heavy water (101) with I E crystals (105) should be used as shown in exploded view Figure 3.
  • the I E crystal (105) provides nucleation sites for the dissolved gases to form bubbles (121) when the pressure is released as seen in Figure 3.
  • the reaction chamber (100) of apparatus (10) in Figure 1 is filled with heavy water (101) containing the dissolved deuterium (102) and oxygen gas (103) as shown in exploded view Figure 2.
  • the pressure is released at valves (111) and (112) as shown in Figure 1, to create bubbles (121) throughout the heavy water (101), each with a radius about 10 microns at 1 atmos pressure in Figure 3.
  • a vacuum is then pulled on the heavy water (101) via valves (111) and (112) and vacuum pump (150) in Figure 4, so that the bubbles (121) expand from the 10 micron radius to the order of 100 to extremely high temperatures which can be as high as 50 eV per particle. This level of temperature is sufficient for fusion to occur.
  • Figure 8 illustrates an alternative method to mix and form deuterium gas (202) and oxygen gas (203) bubbles (221).
  • Deuterium gas (202) and oxygen gas (203) are mixed together precisely at a ratio of 2:1 via tubes (205) and (210) respectively and mix in tube (260) and pass into chamber (240) and pass through holes (220) to form bubbles (221) in heavy water chamber (201).
  • This method of incorporating the bubbles can be incorporated directly into the chamber (100) shown in Figure 1.
  • the energy of the imploding fluid on the bubble increases inversely as the fourth power of the radius.
  • the energy or equivalent pressure increases by 10 8 or one hundred million times.
  • the radius is reduced by a factor of 10 and the energy density of the imploding fluid or its pressure equivalent is increased by 10 4 or ten thousand times or 10 9 Pa according to the equations (2) and (3).
  • the laser is turned on to ignite the deuterium and oxygen gas mixture to form heavy water vapor D 2 0. Then it will expand slightly to eradicate all the asymmetry.
  • the heat of combustion will be cooled off from the surrounding heavy water.
  • the heat of combustion is proportional to the amount of gases (D 2 +l/20 2 ) which is proportional to the volume of the bubble or the cubic power of the radius.
  • the cooling of the heat by the surrounding heavy water is proportional to the surface area of the bubble which varies as the square of the radius.
  • the critical radius can be shown to be:
  • the energy density or its equivalent pressure will increase another ten thousand times to 10 13 Pa. Its temperature equivalent will be above 2 keV.
  • the energy input is tens of keV with the fusion yielding tens of MeV.

Landscapes

  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Abstract

A method of generating nuclear fusion, whereby bubbles of a gas of about 10 micron diameter, contained in heavy water, are expanded by use of a vacuum to about 100 microns in diameter. The subsequent thermal cooling and collapse of the bubbles is augmented by a uniform pressure externally applied and acting on the bubbles through the heavy water. Symmetry in the bubbles' shape is imparted by the addition of heat from a laser as the bubbles continue to contract. High pressures and therefore temperatures are achieved, sufficient to generate nuclear fusion in specific materials.

Description

Title of the Invention
A Method for Generating Nuclear Fusion Through High Pressure
Background of the Invention
The pressure and temperature generated through the collapsing bubbles generated in sonoluminescence is well known. Recently, the creation of micro-thermonuclear fusion by sonoluminescence has been investigated by others and referenced in a number of articles. The first of these to be discussed herein is titled "Sonoluminescence and the prospects for table-top micro-thermonuclear fusion, by W.C. Moss et al.16 Nov 202015 Physics Letters A. In this study, the hydrodynamics of a collapsing bubble were investigated. The addition of pure D20 vapor lowered the speed of sound and this factor, when combined with a pressure spike added to the periodic driving amplitude created temperatures that may be sufficient to generate a very small number of thermonuclear D-D fusion reactions in the bubble. However, the release rate of energy was noted in the article to be in the order of 0.1 counts per second, an extremely small amount.
In the second article, "Shock- Wave Propagation in a Sonoluminescing Gas Bubble" by C.C.Wu et al. 31 May 202013 Physical Review Letters, Wu et al investigated the formation of shocks in a sonoluminous gas bubble of air and determined conditions where the temperature was sufficiently high to create ionization of the air with subsequent release of light energy.
In both of these cases, the expansion and collapse of bubbles comes from the phenomena of sonoluminesence and the high pressure came from shock waves. Furthermore these investigations have not and can not, achieve an energy output in excess of the input. While the results of both of these studies can best be described as a lab curiosity, the present invention describes a viable and effective means to change the structure of materials for the creation of viable micro-thermonuclear fusion, created through the energy of collapsing bubbles.
The present invention investigates the creation of extremely high pressure inside a bubble, not by shock wave alone but by the creation of high pressure due to expansion from rapid heating followed by collapsing due to conduction of heat to the surrounding liquid. While prior methods for which Moss and Wu investigate a curiosity, the current invention is directed towards a commercial method to generate the requisite high pressure needed to generate nuclear fusion as well as a method to generate materials such as metallic hydrogen industrial diamonds and nuclear fusion heat energy.
Also, energy levels of 1 keV are attained by Moss et al, whereas the present invention can attain much higher pressures and high temperatures above the lOkeV levels by external direct compression during the contraction cycle of the bubble, to achieve the higher pressure.
Also in the case of nuclear fusion power, the present invention heats up the entire core of the collapsed bubble, instead of just at the shock front, as in Moss et al. Energy gains are calculated to exceed 1000:1 for the present invention, making it a commercially viable method for generating nuclear fusion power.
Summary of the invention
The pressure from collapsing bubbles can generate sufficient energy to create nuclear energy fusion heat, to generate metallic hydrogen and to generate high- intensity x-rays, produce industrial grade diamonds. While all of the above and many more products can be achieved utilizing the energy of a collapsing bubble, the production of such products have been more of an academic or laboratory curiosity, than a valuable commercial method to generate sufficient quantity of collapsing bubbles for producing commercial quantities of resultant products. The current invention is directed towards a commercially viable product where the output exceeds the costs of input to generate commercial viable quantities of nuclear fusion energy, diamonds, metals and x-rays.
The present invention as applied to the creation of nuclear fusion heat energy conditions in a bubble of deuterium and oxygen in heavy water will generate sufficient energy that far exceeds the input energy. The method involves the creation of bubbles of deuterium and oxygen gas and injecting these bubbles into heavy water, filling a chamber with said deuterium and said oxygen in the heavy water. A vacuum is pulled on the heavy water in the chamber, to generate first the bubbles and then to cause expansion of the bubbles from 10 microns to 100 microns. An external pressure is then applied to the heavy water and subsequently transmitted to the bubbles. The bubbles collapse due to the externally applied pressure. Heating and subsequent expansion of these bubbles at 10 microns is achieved by a laser, which is used to ignite the bubble contents by selecting the correct absorption frequency, thereby imparting symmetry to the bubbles.
The rapid expansion occurring from the ignition is resisted by the progressively applied pressure and removes any assymetry in the bubble surface. Collapse of the bubbles then occurs due to heat transfer to the surrounding heavy water and the increasing externally applied pressure.
In the collapsing of the bubbles in this manner, the necessary pressures and subsequent temperatures for efficient fusion of the deuterium and oxygen, in the order of 5 keV and above can be achieved. Released heat is then transferred to the heavy water for conventional extraction by a heat exchanger.
The present invention can also be applied to the creation of commercially viable new materials such as diamond, high-intensity x-rays and metallic hydrogen under extremely high pressure.
Further, the present invention when utilized with superfliud helium as a media can be used as a method of accelerating particles.
Brief Description of the Drawings
Figure 1 Illustrates an apparatus to practice the method of the invention.
Figure 2 illustrates a bubble of deuterium and oxygen in heavy water.
Figure 3 illustrates bubbles of deuterium and oxygen formed around IE crystals in heavy water.
Figure 4 illustrates the expansion of bubbles due to vacuum.
Figure 5 illustrates application of external pressure to compress the radius of the bubbles.
Figure 6 illustrates laser ignition to impart symmetry to the bubbles.
Figure 7 illustrates the compression of the symmetrical bubble to 1 micron. microns as illustrated in exploded view Figure 4. The precise type of value is not critical.
External pressure (127) is applied by switching on the electro-magnetic plungers (125) of Figure 2 in a controlled manner, the optimum external pressure as a function of time is described in mathematical formulas that are set forth herein and below. The bubbles (121) contract from the 100 micron to about a 10 micron size as illustrated in exploded view Figure 5 by external pressure (122). Ignition of the deuterium-oxygen gas mixture (122) inside each bubble (121) is done by a laser with the right absorption frequency either for deuterium gas or oxygen gas. The external applied heat (131) from the laser (160) in Figure 1 will cause combustion of the deuterium and oxygen gas to heavy water vapor (135) not shown.
The combustion will create high temperature and high pressure inside the bubble (121) to stop the contraction of the bubble from external pressure (127) generated by plungers (125). As shown in Figure 6, the bubbles (121) will expand slightly so that all assymetry created from the hydrodynamic instability of the contraction will be eliminated and symmetry imparted.
The heat from the heavy water vapor (135) will be conducted away by the surrounding heavy water (101). The cooling of the heavy water vapor (135) inside the bubble (121) will cause the vapor (135) to condense on the surface of the bubble (121), creating a low pressure inside the bubble (121) with very little matter.
In Figure 7, the bubble (121) collapses again to less than 1 micron radius. If the water vapor (135), not shown, does not condense on the bubble surface (126) a hard core will be developed and a shock wave will appear. Since the water vapor (135) condenses so that a hard core can not be developed and no shock wave is expected, the continual collapse of the bubble (121) will create ionization of the heavy water (101) Figure 8 illustrates an alternative method for injecting deuterium and oxygen gas.
Description of the Preferred Embodiment
The following is a preferred embodiment for the creation of extreme high pressure. Creation of a mixture of deuterium gas and oxygen gas at the ration of 2:1. The known electrolysis process is applied to heavy water with DC voltage and two electrodes. Heavy water disassociates into deuterium gas and oxygen gas in the cathode and anode respectively, in exactly the ratio of 2:1. They are then gently mixed together to avoid explosion. The exact ratio is important so that when deuterium gas and oxygen gas combust to from heavy water, there is no residual gas.
Introduce the mixture of deuterium gas (102) and oxygen gas (103) in heavy water(lθl) under pressure, as set forth in exploded view Figure 2. The introduction can be by mixing, dissolving any way to introduce the mixture in heavy water. Preferably structured heavy water (101) with IE crystals (105) should be used as shown in exploded view Figure 3. The IE crystal (105) provides nucleation sites for the dissolved gases to form bubbles (121) when the pressure is released as seen in Figure 3.
The reaction chamber (100) of apparatus (10) in Figure 1 is filled with heavy water (101) containing the dissolved deuterium (102) and oxygen gas (103) as shown in exploded view Figure 2. The pressure is released at valves (111) and (112) as shown in Figure 1, to create bubbles (121) throughout the heavy water (101), each with a radius about 10 microns at 1 atmos pressure in Figure 3. A vacuum is then pulled on the heavy water (101) via valves (111) and (112) and vacuum pump (150) in Figure 4, so that the bubbles (121) expand from the 10 micron radius to the order of 100 to extremely high temperatures which can be as high as 50 eV per particle. This level of temperature is sufficient for fusion to occur.
Figure 8 illustrates an alternative method to mix and form deuterium gas (202) and oxygen gas (203) bubbles (221). Deuterium gas (202) and oxygen gas (203) are mixed together precisely at a ratio of 2:1 via tubes (205) and (210) respectively and mix in tube (260) and pass into chamber (240) and pass through holes (220) to form bubbles (221) in heavy water chamber (201). This method of incorporating the bubbles can be incorporated directly into the chamber (100) shown in Figure 1.
The use of this method for the production of metals such as metallic hydrogen, the production of x-rays and diamonds is clearly achievable by using the method as set forth herein and above. For gas containing hydrogen, for example, requires energies at a rninimum of 1 eV from the collapse of the bubble to form metallic hydrogen. For further example such pressure of 1 to 4 eV/atomic volume, will be sufficient for the production of diamonds. X-rays can be produced at 13.6 eV and above, with high intensity x-rays at 1 keV and above. The application of this method to various materials to alter their structure is evident to one skilled in the art. The examples of the embodiment have been set forth above for example and not limitation.
The claims follow the mathematical formulas below.
Mathematical Formulas Illustrating the Invention
Let us consider the maximum rate of the imploding fluid that is collapsing into a bubble. The conservation of matter requires:
4π r2p(r)v(r) = constant Where r is the radius of the bubble, p(r) is the density and v(r) is the velocity of the imploding fluid. The velocity v of the imploding fluid on the bubble is given by: v(r) = v0(po /p) (r2o/r2) (1)
where v0, p0 and ro are the velocity, density and radius of the initial bubble. For an incompressible fluid we have the density constant, (po=p), and the velocity increases as the inverse of the square of the radius. The equivalent pressure p or the kinetic energy density ε is equal to:
ε = p = l/2 p v2 = l/2 p0v0Vo/r4) (2)
Figure imgf000010_0001
where εo= l/2pov0 2
i.e. the energy of the imploding fluid on the bubble increases inversely as the fourth power of the radius. When a bubble decreases from the size of 100 micron to 1 micron, the energy or equivalent pressure increases by 108 or one hundred million times.
So when the bubble is created from the compressed gas inside the heavy water to about a = 10 micron size at one atmosphere (105Pa) a vacuum is pulled by one thousand times less (102Pa), the bubble size will increase approximately to r0= 100 micron. Then we apply external pressure to 1 atmosphere (105Pa). In order to maintain the maximum rate of implosion it is necessary to supply increasing amounts of energy and momentum. The rate of energy increase ε is given by:
ε = 2πp v0V(l- t/tτV4/3 (4) for the increase in energy ε , where t is the time from the contraction of the bubble and tτ is a constant that is equal to total time (tτ = r0/3v0) if the fluid is allowed to collapse inward freely from radius r0 at a velocity v0 to the center of the bubble. If the velocity v0 is about 14 m/s which is the initial velocity that comes from an external pressure of 1 atmosphere (=105 Pa) and r0= 100 microns, the total time tτ = 2.4 s.
When the bubble contracts from 100 microns back to 10 microns the radius is reduced by a factor of 10 and the energy density of the imploding fluid or its pressure equivalent is increased by 104 or ten thousand times or 109 Pa according to the equations (2) and (3). Then the laser is turned on to ignite the deuterium and oxygen gas mixture to form heavy water vapor D20. Then it will expand slightly to eradicate all the asymmetry. The heat of combustion will be cooled off from the surrounding heavy water. The heat of combustion is proportional to the amount of gases (D2+l/202) which is proportional to the volume of the bubble or the cubic power of the radius. The cooling of the heat by the surrounding heavy water is proportional to the surface area of the bubble which varies as the square of the radius. Thus the bigger the bubble, the harder it is to for it to cool and the smaller the bubble the easier for it to cool. The critical radius can be shown to be:
rc = 6Cp pλ7{pg 2v0(q/ ΔT)2}
where:
Cp = specific heat of heavy water p = density of heavy water around the bubble pg = density of the gas inside the bubble v0 = initial velocity from collapse λ = conductivity of the heavy water q = heat of combustion ΔT = temperature difference between the surrounding fluid and the gas
An order of estimate with ΔT ~ 100C yields the value of critical radius to be about 50 microns. Our bubble is about 10 microns when the combustion of deuterium and oxygen gas occurs. So it is smaller than the critical radius. We expect the bubble will cool off and contract again.
When the bubble contracts by another order of magnitude, i.e. from 10 micron to 1 micron, the energy density or its equivalent pressure will increase another ten thousand times to 1013 Pa. Its temperature equivalent will be above 2 keV.
Since the heavy water vapor condenses on the surface of the surrounding fluid, there is no longer a strong hard core because the core will be devoid of vapor and the bubble can collapse to smaller than 1 micron. It can be estimated that if the bubble collapses additionally by 1/3, i.e. 0.36 micron, the energy density will be above 10 keV, a very hot temperature more than enough for nuclear fusion.
The energy input is tens of keV with the fusion yielding tens of MeV. We have a theoretical energy gain of 1000:1. We are different from those nuclear fusion initiated by shock wave ( Moss et al ), where only a small amount will fuse. In our scheme the whole core inside a given radius (which is 0.3 micron in the above case) will undergo nuclear fusion.

Claims

ClaimsI claim:
1. A method for changing the structure of material comprising; introducing a gas in a liquid at high pressure; injecting said gas and liquid into a chamber; reducing chamber pressure allowing the gas to form bubbles throughout the liquid; pulling a vacuum inside said chamber to allow the bubbles to expand; applying an external pressure on said bubbles to reduce said bubbles' volume; adding heat energy to said bubbles to impart symmetry to said bubbles' shape; continuing to apply pressure to said bubbles, further reducing said bubbles' volume until the pressure inside said bubbles exceed the applied pressure.
2. The invention of claim 1 wherein said heat energy is applied utilizing a laser.
3. The invention of claim 1 wherein said heat energy is applied utilizing hydrocarbon.
4. The invention of claim 1 wherein said liquid utilized to introduce said gas in is water.
5. The invention of claim 1 wherein said liquid utilized to introduce said gas in is heavy water.
6. The invention of claim 1 wherein said continuing applying pressure to said bubble further reducing said bubble's volume until the pressure inside said bubbles being a minimum of 1 eV per particle.
u
7. The invention of claim 1 wherein said continuing applying pressure to said bubble further reducing said bubble's volume until the pressure inside said bubbles being a rmriimum of 13.6 eV per particle.
8. The invention of claim 1 wherein said continuing applying pressure to said bubble further reducing said bubble's volume until the pressure inside said bubbles being a miriimum 1 keV per particle.
9. The invention of claim 1 wherein the external pressure is monotonically increasing.
10. The invention of claim 1 wherein said heat energy is generated by an absorption of laser at the characteristic frequency of the material in the bubble.
11. The invention of claim 3 wherein said hydrocarbon is benzene.
12. The invention of claim 6 wherein said gas contains hydrogen.
13. The product of the method of claim 20 being metallic hydrogen
14 The invention of claim 6 wherein the gas contains carbon.
15. The product of the method f the invention of claim 14 being diamond.
16. The product of the invention of claim 7 being x-rays.
17. The product of the invention of claim 8 being high intensity coherent x -rays.
18 The invention of claim 8 wherein gas contains deuterium and oxygen gas.
19. The product of the invention of claim 18 being nuclear fusion heat.
20 A method for changing the structure of materials under high pressure comprising; introducing gas in a liquid at a high pressure; introducing said gas and said liquid into a chamber; reducing said chamber pressure allowing said dissolved gas to form bubbles throughout said liquid; pulling a vacuum inside said chamber to allow said bubbles to expand; applying an external pressure on said bubbles to reduce said bubbles' volume; adding heat energy to the bubbles to impart symmetry in said bubbles' shape; continuing to apply pressure to said bubbles further reducing their volume until the pressure inside the bubbles is a minimum of 1 eV per particle.
21. The invention in claim 20 wherein said gas contains carbon.
22. The invention in claim 20 wherein said gas contains hydrogen.
23. The invention in claim 20 wherein said heat energy is applied utilizing a laser.
24. The invention in claim 20 wherein said heat energy is applied utilizing hydrocarbon.
25. The invention in claim 20 wherein said liquid utilized to introduce said gas in is water.
26. The invention in claim 20 wherein said liquid utilized to introduce said gas in is heavy water.
27. The invention in claim 20 wherein said continuing applying pressure to said bubble further reducing said bubble's volume until the pressure inside said bubble is a minimum of 13.6 eV per particle.
28. The invention of claim 27 wherein the gas contains deuterium gas and oxygen gas.
29. The product of the invention of claim 28 being coherent x-rays.
30. The invention in claim 20 wherein said continuing applying pressure to said bubble further reducing said bubble's volume until the pressure inside said bubble is a minimum of 1 KeV per particle.
31. The invention in claim 20 wherein the external pressure is monotonically increasing.
32. The invention in claim 20 wherein said heat energy is generated by an absorption of laser at the characteristic frequency of the material in the bubble.
33. The invention of claim 24 wherein said hydrocarbon is benzene.
34 The invention of claim 27 wherein said gas contains deuterium gas and oxygen gas.
35. The invention of claim 32 wherein said deuterium gas and said oxygen gas is ignited to form heavy water gas.
36 The invention of claim 20 wherein said gas contains deuterium gas and oxygen gas. 37. A method for generating high pressure inside a bubble, comprising; generating bubbles in a fluid; contracting said bubbles in said fluid by external pressure; applying heat during the compression to impart symmetry. 38. The product of the invention of claim 37 being nuclear fusion heat.
PCT/US1997/010012 1996-06-11 1997-06-11 A method for generating nuclear fusion through high pressure WO1997049274A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU33842/97A AU3384297A (en) 1996-06-11 1997-06-11 A method for generating nuclear fusion through high pressure

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US66175996A 1996-06-11 1996-06-11
US08/661,759 1996-06-11

Publications (1)

Publication Number Publication Date
WO1997049274A2 true WO1997049274A2 (en) 1997-12-31

Family

ID=24655003

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1997/010012 WO1997049274A2 (en) 1996-06-11 1997-06-11 A method for generating nuclear fusion through high pressure

Country Status (2)

Country Link
AU (1) AU3384297A (en)
WO (1) WO1997049274A2 (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001039203A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039206A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039201A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039200A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039199A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Enhancing electrolytic cavitation reactions
WO2001039198A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor system
WO2001039197A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2003077260A2 (en) * 2002-03-12 2003-09-18 General Fusion Inc. Apparatus and method for fusion reactor
US7381241B2 (en) 1999-11-24 2008-06-03 Impulse Devices, Inc. Degassing procedure for a cavitation chamber
US7387660B2 (en) 1999-11-24 2008-06-17 Impulse Devices, Inc., Degassing procedure for a cavitation chamber
US7448790B2 (en) 1999-11-24 2008-11-11 Impulse Devices, Inc. Cavitation fluid circulatory system for a cavitation chamber
US8891719B2 (en) 2009-07-29 2014-11-18 General Fusion, Inc. Systems and methods for plasma compression with recycling of projectiles
ITUD20130067A1 (en) * 2013-05-21 2014-11-22 Gian Luigi Bortolussi PLANT AND METHOD FOR THE PRODUCTION OF NUCLEAR FUSION ENERGY
US9424955B2 (en) 2009-02-04 2016-08-23 General Fusion Inc. Systems and methods for compressing plasma
US10002680B2 (en) 2005-03-04 2018-06-19 General Fusion Inc. Pressure wave generator and controller for generating a pressure wave in a liquid medium
US10115486B2 (en) 2015-03-11 2018-10-30 General Fusion Inc. Modular compression chamber
US11028686B2 (en) 2019-06-12 2021-06-08 Saudi Arabian Oil Company Sono tool and related systems and methods

Cited By (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001039197A3 (en) * 1999-11-24 2003-02-20 Impulse Devices Inc Cavitation nuclear reactor
US7448790B2 (en) 1999-11-24 2008-11-11 Impulse Devices, Inc. Cavitation fluid circulatory system for a cavitation chamber
WO2001039201A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039200A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039199A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Enhancing electrolytic cavitation reactions
WO2001039204A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Shaped core cavitation nuclear reactor
WO2001039203A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039197A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039205A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
WO2001039206A3 (en) * 1999-11-24 2002-04-25 Impulse Devices Inc Cavitation nuclear reactor
WO2001039201A3 (en) * 1999-11-24 2002-07-04 Impulse Devices Inc Cavitation nuclear reactor
WO2001039199A3 (en) * 1999-11-24 2002-07-18 Impulse Devices Inc Enhancing electrolytic cavitation reactions
WO2001039200A3 (en) * 1999-11-24 2002-09-26 Impulse Devices Inc Cavitation nuclear reactor
WO2001039198A3 (en) * 1999-11-24 2002-09-26 Impulse Devices Inc Cavitation nuclear reactor system
WO2001039205A3 (en) * 1999-11-24 2002-11-21 Impulse Devices Inc Cavitation nuclear reactor
WO2001039204A3 (en) * 1999-11-24 2002-11-28 Impulse Devices Inc Shaped core cavitation nuclear reactor
WO2001039198A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor system
WO2001039203A3 (en) * 1999-11-24 2003-02-20 Impulse Devices Inc Cavitation nuclear reactor
WO2001039206A2 (en) * 1999-11-24 2001-05-31 Impulse Devices, Inc. Cavitation nuclear reactor
US7387660B2 (en) 1999-11-24 2008-06-17 Impulse Devices, Inc., Degassing procedure for a cavitation chamber
US7381241B2 (en) 1999-11-24 2008-06-03 Impulse Devices, Inc. Degassing procedure for a cavitation chamber
WO2003077260A3 (en) * 2002-03-12 2003-11-13 Gen Fusion Inc Apparatus and method for fusion reactor
WO2003077260A2 (en) * 2002-03-12 2003-09-18 General Fusion Inc. Apparatus and method for fusion reactor
US10002680B2 (en) 2005-03-04 2018-06-19 General Fusion Inc. Pressure wave generator and controller for generating a pressure wave in a liquid medium
US9424955B2 (en) 2009-02-04 2016-08-23 General Fusion Inc. Systems and methods for compressing plasma
US9875816B2 (en) 2009-02-04 2018-01-23 General Fusion Inc. Systems and methods for compressing plasma
US10984917B2 (en) 2009-02-04 2021-04-20 General Fusion Inc. Systems and methods for compressing plasma
US8891719B2 (en) 2009-07-29 2014-11-18 General Fusion, Inc. Systems and methods for plasma compression with recycling of projectiles
US9271383B2 (en) 2009-07-29 2016-02-23 General Fusion, Inc. Systems and methods for plasma compression with recycling of projectiles
ITUD20130067A1 (en) * 2013-05-21 2014-11-22 Gian Luigi Bortolussi PLANT AND METHOD FOR THE PRODUCTION OF NUCLEAR FUSION ENERGY
US10115486B2 (en) 2015-03-11 2018-10-30 General Fusion Inc. Modular compression chamber
US11028686B2 (en) 2019-06-12 2021-06-08 Saudi Arabian Oil Company Sono tool and related systems and methods

Also Published As

Publication number Publication date
AU3384297A (en) 1998-01-14

Similar Documents

Publication Publication Date Title
WO1997049274A2 (en) A method for generating nuclear fusion through high pressure
US4333796A (en) Method of generating energy by acoustically induced cavitation fusion and reactor therefor
US3808432A (en) Neutral particle accelerator utilizing radiation pressure
Olson et al. First liquid layer inertial confinement fusion implosions at the national ignition facility
Sacks et al. Direct drive cryogenic ICF capsules employing DT wetted foam
Haines et al. The past, present, and future of Z pinches
Gus' Kov et al. Similarity solution of thermonuclear burn wave with electron and α-conductivities
US5041760A (en) Method and apparatus for generating and utilizing a compound plasma configuration
US5015432A (en) Method and apparatus for generating and utilizing a compound plasma configuration
US20070002996A1 (en) Tabletop nuclear fusion generator
Zhou et al. Hydrodynamic relations for direct-drive fast-ignition and conventional inertial confinement fusion implosions
US4252607A (en) Radiation source
US20030215046A1 (en) Pressure generating structure
CN101496111A (en) Method and system for controlled fusion reactions
Dhakal et al. Effects of thermal conductivity of liquid layer in NIF wetted foam experiments
WO2001039197A2 (en) Cavitation nuclear reactor
US20070206714A1 (en) Propulsion motor
Slutz et al. Radiation driven capsules for fast ignition fusion
Van Dael Experimental investigation of thermomagnetic torques in dilute nitrogen
Meeker et al. A high efficiency ICF driver employing magnetically confined plasma rings
Linhart Magnetically Imploded Plasma as a Driver for ICF
Zadfathollah et al. Implosion Plasma Driven Fusion Pellet of Inertial Confinement (A Short Memorandum)
GS et al. IMPLOSION, STABILITY, AND BURN OF MULTISHELL FUSION PELLETS
US20200335229A1 (en) Thermo-kinetic reactor with micro-nuclear implosions
Nuckolls Early steps toward inertial fusion energy (IFE)(1952 to 1962)

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AL AM AT AT AU AZ BB BG BR BY CA CH CN CZ CZ DE DE DK DK EE EE ES FI FI GB GE GH HU IL IS JP KE KG KP KR KZ LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SK TJ TM TR TT UA UG US UZ VN YU AM AZ BY KG KZ MD RU TJ TM

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GH KE LS MW SD SZ UG ZW AT BE CH DE DK ES FI FR GB GR IE IT LU

WA Withdrawal of international application
121 Ep: the epo has been informed by wipo that ep was designated in this application
122 Ep: pct application non-entry in european phase
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

NENP Non-entry into the national phase

Ref country code: CA