CONVERSION OF VIBRATIONAL ENERGY
20170173552 ยท 2017-06-22
Inventors
- Peter L. Hagelstein (Carlisle, MA, US)
- Michael MCKUBRE (Menlo Park, CA, US)
- Jianer Bao (Sunnyvale, CA, US)
- Francis L. TANZELLA (San Carlos, CA, US)
Cpc classification
G21B3/00
PHYSICS
B01J19/10
PERFORMING OPERATIONS; TRANSPORTING
H05G2/00
ELECTRICITY
G21H1/00
PHYSICS
H03B5/30
ELECTRICITY
International classification
B01J19/10
PERFORMING OPERATIONS; TRANSPORTING
H05G2/00
ELECTRICITY
Abstract
The present application discloses methods and apparatus for conversion of quantized vibrational energy. The present application discloses, by driving a medium that comprises arranged nuclei with one or more selected driving frequencies, the arranged nuclei in the medium are induced to oscillate coherently at one or more oscillating frequencies. The mechanical vibrational energy of the oscillating nuclei interacts with the oscillating medium. The interaction between the vibrational energy and the oscillating medium effectuates up-conversion or down-conversion of quantized vibrational energy.
Claims
1. An apparatus comprising: a driver for generating oscillations; and a medium comprising arranged nuclei configured to oscillate at one or more oscillating frequencies when the medium is driven by the driver, wherein vibrational quanta are either down-converted or up-converted due to interaction between vibrational energy of the oscillating nuclei and the oscillating nuclei, wherein, when the vibrational quanta are up-converted, the vibrational energy is converted to increase energy of conduction charges in the medium, and wherein one or more of the conduction charges overcome the surface energy barrier of the medium or become available for charge transfer to atoms or molecules in contact with a surface of the medium.
2. The apparatus of claim 1, wherein the oscillating nuclei comprise stable nuclei that can be excited onto one or more unstable states, and wherein, when the vibrational quanta are up-converted, the vibrational energy excites the stable nuclei to the one or more unstable states from which the excited nuclei undergo nuclear decay.
3. (canceled)
4. The apparatus of claim 1, wherein, when the vibrational quanta are down-converted, nuclear energy or electronic energy is converted to vibrational energy of the oscillating nuclei.
5. The apparatus of claim 1, wherein the oscillations generated by the driver are of one or more driving frequencies between 100 KHz and 50 THz.
6. The apparatus of claim 4, wherein the medium comprises a metal plate and the driver is connected to a signal generator via an amplifier, the signal generator generating a signal of a selected frequency; wherein the signal generator, via the amplifier, applies a drive voltage between the driver and the metal plate, the drive voltage creating an electrostatic coupling between the driver and the metal plate; and wherein the metal plate is induced to vibrate by the electrostatic coupling and wherein the vibrating metal plate is configured to emit the conduction charges that overcome the surface energy barrier of the metal plate.
7. The apparatus of claim 6, wherein the selected frequency is set to be one half of a resonant frequency of the metal plate and wherein the resonant frequency of the metal plate is associated with a compressional or transverse vibrational mode of the metal plate.
8. The apparatus of claim 6, wherein the metal plate is further attached to a resonator to arrange for a large number of nuclei to oscillate coherently.
9. The apparatus of claim 6, wherein the metal plate is connected to a collector that collects the charges emitted by the vibrating metal plate.
10. The apparatus of claim 6, wherein the metal plate is made of a metal selected from the group of copper, aluminum, nickel, titanium, palladium, tantalum, and tungsten.
11. The apparatus of claim 6, wherein the driver is connected to a copper pole for support, wherein the length of the driver is between 0.20-0.30 inches and the diameter of the driver is between 0.7-0.8 inches, the thickness of the metal plate is between 70-80 microns, and the distance between the driver and the metal plate is between 10-100 microns.
12. The apparatus of claim 8, wherein the driver is coated with Polyvinylidene Fluoride (PVDF) to prevent air breakdown, and wherein the distance between the driver and the metal plate is approximately 20 microns.
13. A method of converting vibrational quanta, comprising: generating oscillations using a driver; driving a medium comprising arranged nuclei to oscillate at one or more oscillating frequencies; and down-converting or up-converting vibrational quanta due to interaction between vibrational energy of the oscillating nuclei and the oscillating nuclei, wherein the oscillations generated by the driver are of one or more driving frequencies between 100 KHz and 50 THz.
14. (canceled)
15. The method of claim 13, wherein the arranged nuclei comprise stable nuclei that can be excited onto one or more unstable states, and wherein the up-converting of vibrational quanta comprises exciting the stable nuclei onto the one or more unstable states from which the excited nuclei undergo nuclear decay.
16. The method of claim 13, wherein, when the vibrational quanta are up-converted, the vibrational energy is converted to increase the energy of conduction charges in the medium.
17. The method of claim 16, wherein the medium is a metal plate and one of the one or 5 more oscillating frequency is a resonant frequency of the metal plate, and wherein the vibrational quanta in the vibrating metal plate are up-converted into energy of conduction charges in the metal plate and the vibrating metal plate is configured to emit one or more of the conduction charges that comprise electrons or molecular ions.
18. The method of claim 17, further comprising collecting the one or more of conduction charges using a collector, wherein the conduction charges comprise electrons or molecular ions.
19. The method of claim 18, further comprising directing the collected charges to a confined region where a chemical reaction is taking place, to accelerate the chemical reaction.
20. (canceled)
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0017]
[0018]
[0019]
[0020]
[0021]
[0022]
[0023]
DETAILED DESCRIPTION
[0024]
[0025] The signal generator 106 is configured to generate signals for driving the driver 104. The driving signals generated by the signal generator 106 may comprise signals of one or more frequencies. In some embodiments, an Agilent 8648A RF Function generator is used to generate radio signals from 1 to 61 MHz, and an ENI 603L 3-W linear amplifier is used as the amplifier 108 to amplify the driving signals. In one embodiment, a power gain of 40 dB is achieved by the amplifier 108. The driving signal applies a driving voltage between the driver 104 and the grounded metal plate 102, creating an electrostatic coupling between the driver and the metal plate 102. Because of the electrostatic coupling, the metal plate 102 is induced to vibrate in response to the driving signal.
[0026] In some embodiments, when the driving frequencies are set to one or more selected values, the quantum effect of the vibrational energy of the metal plate is manifested. The apparatus 100 is configured to convert the quantized vibrational energy into the energy of the electrons in the metal plate. In these embodiments, the driver 104 in the apparatus 100 is constructed using a thick cylinder 202 connected to a rod 204, as shown in
[0027] The metal plate 102 is made of copper foil and is in the shape of a circle. In one embodiment, the thickness of the copper foil is between 72 and 73 microns and the diameter of the copper foil is approximately 1.5 inches. However, the copper foil can be made of a different thickness, for example, between 10-200 microns. The metal plate 102 may be made of rolled or annealed copper.
[0028] As an enhancement, a resonator 304 may be attached to the metal plate 102 as shown in
[0029] When the signal generator 106 is turned on, through the electrostatic coupling between the driver 104 and the resonator assembly 302, the resonator assembly 302 is induced to vibrate in response to the driving signal. Mechanical vibrations in the resonator assembly 302 are driven by the force exerted on the metal plate 102. The force is due to the electric field between the driver 104 and the metal plate 102. As an approximation, the driver 104 and the resonator assembly 302 can be treated as an air capacitor with two parallel plates. The electric field in between the plates can be viewed as normal to the surfaces of the plates and of a uniform magnitude. Near the edges of the plates, the magnitude of the electric field falls off quickly. Under the assumption that the driver 104 and the resonator assembly 302 form a uniform planar capacitor, the force exerted on the resonator assembly 302 can be expressed as:
where A is the area of the planar capacitor, d is the distance between the parallel plates of the planar capacitor, is the dielectric coefficient, and V is the driving voltage applied to the capacitor by the signal generated by the signal generator 106. As can be seen in Eq (1), the force exerted on the resonator assembly 302 is proportional to V.sup.2. Therefore, the frequency of the force (or the frequency of a component of the force) is twice the frequency of the driving voltage. It is noted that in embodiments in which a DC offset is included in the driving voltage, a component of the force is proportional to V multiplied by the DC offset. In such case, the frequency of that force component is the same as the frequency of the driving voltage. Because the force drives the vibration of the resonator plate, herein the frequency of the force is referred to as the driving frequency. It is noted that the driving frequency may be twice the frequency of the signal generated by the signal generator 106. The frequency at which the resonator assembly 302 vibrates is referred to as the oscillating frequency of the resonator assembly 302.
[0030] When the driving frequency matches one of the resonant frequencies of the resonator assembly 302, the resonator assembly 302 vibrates in one of the resonant modes. The resonant modes of the resonator assembly 302 include fundamental compressional modes in which the resonator assembly 302 vibrates along the longitudinal axis of the resonator 304. The resonant modes of the resonator assembly 302 also include fundamental transverse modes in which the vibrations are along the radial direction. The resonant modes also include combinations of the fundamental compressional modes and transverse modes.
[0031] The vibrational movements of the metal plate 102 can be approximated using an elastic model:
where u is the displacement of a point (any point) on the metal plate 102, is the density of the metal plate at that point, and are elastic constants, and f is the force density. In Eq (2), term (+).sup.2u represents the compressional movements and term (u) represents the transverse movements of the metal plate 102.
[0032] The frequencies of the fundamental compressional modes can be expressed as
where n is the order of the resonant mode and c is the speed of the mechanical waves traveling across the metal plate 102. The frequencies of the transverse modes can be expressed as ={square root over (c.sup.2[k.sub.x.sup.2+k.sub.y.sup.2])} with k.sub.x and k.sub.y representing components of a wave vector along the x and y directions (i.e., two perpendicular radial directions) respectively.
[0033] When the resonator assembly 302 vibrates in a resonant mode, the different parts of the resonator plate move coherently and the vibrational energy is maximized within the vicinity of the resonant mode (i.e., a local maximum). In some embodiments, when the signal generator 106 is configured to generate a signal of frequency v with v being half of a resonant frequency of the metal plate 102, the metal plate 102 is induced to vibrate in the resonant mode having a resonant frequency 2v. When in a resonant mode, the quantum effect of the vibrational energy of the metal plate 102 may be manifested and the vibrational quanta may be converted into the electronic energy of the conduction charges in the metal plate 102. Examples of the conduction charges include electrons. In some cases, when the vibrational energy of the metal plate 102 is converted into the energy of the electrons, one or more of the energized electrons may overcome the surface energy barrier of the metal plate 102 and break free from the metal plate 102. It is noted that in some embodiments in which the plate 102 is made of semiconductor instead of metal, the conduction charges may be holes. In these embodiments, one or more of the promoted or excited holes may transfer charges to atoms or molecules that come in contact with the surface of the medium.
[0034] To collect the electrons emitted by the metal plate 102, a collector 402 may be placed near the resonator assembly 302 as shown in
[0035]
[0036]
[0037]
[0038]
[0039] In the above described embodiments, the vibrational energy of the metal plate 102 is converted into the electronic energy of the conduction charges in the metal plate 102. In some embodiments, the vibrational energy of the metal plate 102 may be converted into nuclear energy. In one embodiment, the metal plate 102 in the resonator assembly 302 is coated with mercury (Hg) to facilitate conversion of the vibrational energy into nuclear energy. It is known that a .sup.201Hg nucleus has an excited nuclear state that is1.5648 keV above the ground stable state (i.e., lowest energy nuclear transition). Through the interaction between the vibrational energy and the oscillating mercury nuclei, the vibrational quanta are converted into the nuclear energy of the .sup.201Hg nuclei. The .sup.201Hg nuclei are pumped onto the excited nuclear state. The excited .sup.201Hg nuclei undergo nuclear decay by exiting the excited state, which has a half-life of 81 ns (4 ms if only radiative decay occurs).
[0040] To prepare a mercury-coated metal plate 102, the first step is to plate mercury on the surface of the metal plate 102, e.g., a copper foil. Mercury ions readily diffuse into the copper foil, forming an amalgam. The foil is then treated with an oxidation-reduction process using a saturated Hg.sub.2SO.sub.4/H.sub.2O solution. The Hg.sub.2SO.sub.4/H.sub.2O solution is prepared by mixing an excess of Hg.sub.2SO.sub.4 in H.sub.2O and stirring overnight. The mercury-plated copper foil is cleaned using acetone and de-ionized water, and then dipped into a diluted H.sub.2SO.sub.4 solution (with a pH value smaller than 1) for approximately one minute to remove the oxide. The copper foil is then rinsed with de-ionized water again. When both sides of the copper foil are coated with mercury, the copper foil is dipped into the saturated Hg.sub.2SO.sub.4 solution for approximately one minute and then rinsed with de-ionized water. If only one side of the copper foils is coated with mercury, the copper foil is laid flat on a glass surface and a cotton swap soaked with the saturated Hg.sub.2SO.sub.4 solution is used to wet the top surface of the copper foil. After approximately two minutes, the surface of the copper foil would show a pale white or silvery hue. The copper foil is then rinsed with de-ionized water and dried. The above oxidation-reduction reaction can be express as:
Hg.sup.2+Cu=Hg+Cu.sup.2+.
[0041] In some embodiments, the mercury coated copper foil is used as the metal plate 102 in the resonator assembly 302. X-ray emissions are recorded by an X-ray detector when the resonator assembly 302 is connected to the driver 102 in a system set up similarly to that shown in
[0042] Because of the high driving frequency, the level of mechanical vibration may exceed the breakdown strength of air. To prevent air breakdown, the driver 104 is coated with a layer of Polyvinylidene Fluoride (PVDF). When the driver 104 is coated with PVDF, the driver 104 can be set up in contact with the metal plate 102, in which case the resonant frequency of the transverse mode of the resonator assembly 302 may be lower. For example, in the above described electron emission results shown in
[0043] In some embodiments, X-ray emissions with energies between 1.34 keV and 1.6 keV are recorded by the X-ray detector. In one embodiment, the driver 104 is configured with round edges and the driving frequency is set to 14.7 MHz with a drive voltage of 90V rms. X-ray emissions are recorded near 1.34 keV. In one embodiment, the driver 104 is shaped with sharp edges and the driving frequency is set to 14.7 MHz with a drive voltage of 100V rms. X-ray emissions are recorded near 1.6 keV. In these embodiments, the distance between the driver 104 and the resonator assembly 302 varies from 40 microns to 0 microns when the PFDV coated drive 102 is in contact with the resonator assembly 302.
[0044] The observed X-ray emissions are due to nuclear decay of the excited .sup.201Hg nuclei. The nuclear energy gained by the .sup.201Hg nuclei when being pumped onto the excited state is derived from the quantized vibrational energy of the vibrating resonator plate 320. Through the interaction between the vibrational energy of the metal plate and the .sup.201Hg nuclei, the vibrational quanta are up-converted into nuclear energy.
[0045] In the embodiments described above, vibrational quanta are up-converted into nuclear energy or electronic energy. Vibrational quanta can be down-converted as well.
[0046]
[0047] The present invention may, of course, be carried out in other ways than those specifically set forth herein without departing from essential characteristics of the invention. The present embodiments are to be considered in all respects as illustrative and not restrictive, and all changes coming within the meaning and equivalency range of the appended claims are intended to be embraced therein.