JPH0353195A - Energy generator - Google Patents
Energy generatorInfo
- Publication number
- JPH0353195A JPH0353195A JP1187531A JP18753189A JPH0353195A JP H0353195 A JPH0353195 A JP H0353195A JP 1187531 A JP1187531 A JP 1187531A JP 18753189 A JP18753189 A JP 18753189A JP H0353195 A JPH0353195 A JP H0353195A
- Authority
- JP
- Japan
- Prior art keywords
- electrode
- palladium
- power source
- porous structure
- palladium electrode
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims abstract description 119
- 229910052763 palladium Inorganic materials 0.000 claims abstract description 59
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 32
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 claims description 20
- 239000002245 particle Substances 0.000 claims description 4
- 239000011148 porous material Substances 0.000 claims description 3
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 2
- 238000005245 sintering Methods 0.000 claims description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 abstract description 13
- 229910052805 deuterium Inorganic materials 0.000 abstract description 12
- 238000006243 chemical reaction Methods 0.000 abstract description 10
- 230000002776 aggregation Effects 0.000 abstract description 5
- 238000004220 aggregation Methods 0.000 abstract description 5
- 238000005868 electrolysis reaction Methods 0.000 abstract 1
- 150000002940 palladium Chemical class 0.000 abstract 1
- 239000003513 alkali Substances 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- -1 lithium chloride Chemical class 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21B—FUSION REACTORS
- G21B3/00—Low temperature nuclear fusion reactors, e.g. alleged cold fusion reactors
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E30/00—Energy generation of nuclear origin
- Y02E30/10—Nuclear fusion reactors
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- General Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
- Electrolytic Production Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
（産業上の利用分野）
本発明は簡単な構成によるエネルギー発生装置に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an energy generating device with a simple configuration.
（従来の技術）
従来、エネルギー発生装置としての重水素反応装置は，
高温、高圧下において、重水素一重水素を融合反応させ
ることにより行わせていた。(Prior art) Conventionally, a deuterium reactor used as an energy generating device was
It was carried out by fusion reaction of monodeuterium at high temperature and pressure.
（発明が解決しようとするＨＭ）
しかしながら、上記従来の重水素反応装置は、極めて高
価な設備を必要とし，しかも極めて効率が悪い等の欠点
があった。(HM to be Solved by the Invention) However, the conventional deuterium reactor described above requires extremely expensive equipment and has drawbacks such as extremely low efficiency.
本発明は上記の欠点をなくし、極めて簡単な方法により
，安価に反応を行わしめることによる、エネルギー発生
装置を提供することを目的とするものである。SUMMARY OF THE INVENTION An object of the present invention is to eliminate the above-mentioned drawbacks and to provide an energy generating device that can carry out reactions at low cost using an extremely simple method.
（課題を解決するための手段）
本発明は上記目的を達或するために，重水及びアルカリ
ハライドから成る溶液と，白金電極，パラジウム電極，
電源とから構威した装置を用い、白金電極を陽極、パラ
ジウム電極を凸凹の大きい多孔質構造の陰電極として電
気エネルギーを供給することにより、パラジウム電極表
面に大量のエネルギーを発生させるもので，このとき，
バラジウム電極表面を超音波振動させることにより、ま
た，パラジウム電極表面を多孔質構造に形成せしめるこ
とによって、極めて高効率のエネルギー発生を行わせる
ことができることを発見したことに基づいている。(Means for Solving the Problems) In order to achieve the above object, the present invention uses a solution consisting of heavy water and an alkali halide, a platinum electrode, a palladium electrode,
This method generates a large amount of energy on the surface of the palladium electrode by supplying electrical energy to the platinum electrode as an anode and the palladium electrode as a cathode with a highly uneven porous structure using a device constructed from a power source. When,
This method is based on the discovery that energy can be generated with extremely high efficiency by subjecting the palladium electrode surface to ultrasonic vibration and by forming the palladium electrode surface into a porous structure.
（作 用）
したがって本発明によれば、重水と、白金電極、パラジ
ウム電極、電源とから構成した装置を用い、白金電極を
陽極，パラジウム電極を陰極として電気エネルギーを供
給することにより，パラジウム電極表面に大量のエネル
ギーを発生させるもので、このとき，パラジウム電極表
面を超音波振動させることにより，パラジウム電極表面
にキャビテーションを生じさせ、これにより該電極表面
に高圧高温状態を生じさせ，重水素の凝集反応を効果的
に高め，それと同時に，パラジウム電極表面を多孔質構
造に形成せしめ，電極表面積を実効的に大きくシ，かつ
，反応を最も効果的にする粒径０．ｌ〜１００ミクロン
の大きさに設定することによって，極めて高効率のエネ
ルギー発生を行わせることができる．
（実施例）
第１図は本発明のー．実施例におけるエネルギー発生装
置の概略を示している．第１図において、１は高温に耐
える磁器等から成る容器，２は重水及び塩化リチウム等
のアルカリハライド等から成る溶液，３は電源の陽極に
接続された白金電極、４は電源の陰極に接続されたパラ
ジウム電極，５は電源、６は圧電振動子、７は出力電圧
１０数ボルトの圧電振動子用電源である。(Function) Therefore, according to the present invention, by using a device composed of heavy water, a platinum electrode, a palladium electrode, and a power source, and supplying electrical energy with the platinum electrode as an anode and the palladium electrode as a cathode, the surface of the palladium electrode is At this time, the palladium electrode surface is vibrated ultrasonically to generate cavitation on the palladium electrode surface, which creates a high-pressure and high-temperature state on the electrode surface, which causes the aggregation of deuterium. At the same time, the palladium electrode surface is formed into a porous structure to effectively increase the electrode surface area, and the particle size is 0.00 to make the reaction most effective. By setting the size to 1 to 100 microns, it is possible to generate energy with extremely high efficiency. (Example) Figure 1 shows the embodiment of the present invention. This figure shows an outline of the energy generation device in the example. In Figure 1, 1 is a container made of porcelain that can withstand high temperatures, 2 is a solution made of heavy water and an alkali halide such as lithium chloride, 3 is a platinum electrode connected to the anode of the power source, and 4 is connected to the cathode of the power source. 5 is a power source, 6 is a piezoelectric vibrator, and 7 is a power source for the piezoelectric vibrator with an output voltage of 10-odd volts.
容器１に溶液２を入れ，白金電極３及びパラジウム電極
４を配し電源５のよって電力を供給する．パラジウム電
極４は圧電振動子６と一体になっており、圧電振動子６
は圧電振動子用電源７に電気的に接続されている．電源
５のスイッチを入れると同時に，重水の溶液２は電気分
解を開始し，重水素はパラジウム電極４の表面に集まる
。この時パラジウム電極４の表面に多量の熱量が発生す
る．実験によると、ｖｅ．ｇとして１０数ボルト、２０
数時間後に印加熱量の約５０％増の熱量が発生した。こ
こで、圧電振動子用電源７のスイッチを入れると、３０
数ミリアンペアの電流が流れ圧電振動子６は２０数キロ
ヘルツで振動を開始する．圧電振動子６が、強力な超音
波を発生すると、圧電振動子６と一体となったパラジウ
ム電極４も，同時は超音波振動し、該パラジウム電極４
の表面では、強力なキャビテーションが起こる。この強
力なキャビテーションにより，該パラジウム電極４の表
面では、非常に大きな圧力と、高温度の状態となる．そ
のため，該パラジウム電極４の表面での重水素の凝集反
応が急激に進む．この結果，該パラジウム電極４の表面
での発生熱量は、キャビテーションのない場合に比べ，
約６０％の上昇となった。A solution 2 is placed in a container 1, a platinum electrode 3 and a palladium electrode 4 are arranged, and power is supplied from a power source 5. The palladium electrode 4 is integrated with the piezoelectric vibrator 6, and the piezoelectric vibrator 6
is electrically connected to the piezoelectric vibrator power supply 7. As soon as the power source 5 is turned on, the heavy water solution 2 starts electrolyzing, and deuterium collects on the surface of the palladium electrode 4. At this time, a large amount of heat is generated on the surface of the palladium electrode 4. According to experiments, ve. g as 10-odd volts, 20
After several hours, an amount of heat approximately 50% higher than the amount of applied heat was generated. Here, when the piezoelectric vibrator power supply 7 is turned on, 30
A current of several milliamps flows, and the piezoelectric vibrator 6 begins to vibrate at a frequency of 20-odd kilohertz. When the piezoelectric vibrator 6 generates strong ultrasonic waves, the palladium electrode 4 integrated with the piezoelectric vibrator 6 simultaneously vibrates ultrasonically, and the palladium electrode 4
Strong cavitation occurs on the surface of This strong cavitation creates extremely high pressure and high temperature on the surface of the palladium electrode 4. Therefore, the aggregation reaction of deuterium on the surface of the palladium electrode 4 rapidly progresses. As a result, the amount of heat generated on the surface of the palladium electrode 4 is lower than that in the case without cavitation.
This was an increase of about 60%.
第２図は本発明の第ｌ図のパラジウム電極４の断面を示
したものである。第２図において、４はパラジウム電極
、１１は凸凹をつけた多孔貿構造表面である．
次に上記実施例の動作について説明する。上記実施例に
おいて，通電時のパラジウム電極４の表面では，重水素
Ｄによる凝集反応が起こっており，そのため多量の熱量
が発生していると考えられる．この時，パラジウム電極
４の表面を多孔質にすると，この反応は益々起こり易く
なると考えられる．そこで，この多孔質構造パラジウム
電極を形或するのに，パラジウム粉末を窒素雰囲気中、
１３００〜１６００℃で焼結形或することによりＩ２造
したところ、極めて高効率の反応が進行することが確認
できた。FIG. 2 shows a cross section of the palladium electrode 4 of FIG. 1 of the present invention. In Fig. 2, 4 is a palladium electrode, and 11 is a porous textured surface with irregularities. Next, the operation of the above embodiment will be explained. In the above example, it is thought that a coagulation reaction due to deuterium D occurs on the surface of the palladium electrode 4 when electricity is applied, and therefore a large amount of heat is generated. At this time, it is thought that if the surface of the palladium electrode 4 is made porous, this reaction will occur more easily. Therefore, in order to form this porous structure palladium electrode, palladium powder was mixed in a nitrogen atmosphere.
When I2 was manufactured by sintering at 1300 to 1600°C, it was confirmed that the reaction proceeded with extremely high efficiency.
またこの時得られた電極のパラジウム粒径は，０．１〜
１００ミクロンの大きさの時、最も効率がよかった．ま
た孔径は、平均ｌＯミクロン（０．１〜５００ミクロン
）程度であった。実験によると、この多孔質構造パラジ
ウム電極を用いると、多孔貿でない場合に比べ，発生熱
量は、５〜１０％増の値が得られた．このような構成の
多孔質構造パラジウム電極では，電極表面積が実効的に
大きく、重水素の凝集反応が高効率で進むことによるも
のと思われる。Moreover, the palladium particle size of the electrode obtained at this time was 0.1~
The efficiency was highest when the size was 100 microns. Moreover, the average pore diameter was about 10 microns (0.1 to 500 microns). According to experiments, when this porous structure palladium electrode was used, the amount of heat generated was 5 to 10% higher than that without the porous structure. This is thought to be due to the fact that in the porous structure palladium electrode having such a configuration, the electrode surface area is effectively large, and the aggregation reaction of deuterium proceeds with high efficiency.
第３図は，本発明の他の実施例におけるエネルギー発生
装置の概略を示す図である。第３図における数字は第１
図のそれぞれと一致させてある。FIG. 3 is a diagram schematically showing an energy generating device in another embodiment of the present invention. The numbers in Figure 3 are number 1.
They are matched with each of the figures.
第３図において、容器１内に重水及び塩化リチウム等の
アルカリハライド等からなる溶液２を入れ，白金電極３
及びパラジウム電極４を配し、電源５の陽極及び陰極に
接続し電力を供給する。圧電振動子６は容器１の外壁に
接着して取りつけられており，圧電振動子６は圧電振動
子用電源７に電気的に接続されている。ここで、圧電振
動子用電源７のスイッチを入れると，圧電振動子６は振
動を開始する。圧電振動子６が．強力な超音波を発生す
ると、この超音波の焦点の位置に取り付けられているパ
ラジウム電極４も、同時に超音波振動し、該パラジウム
電極４の表面では、強力なキャビテーションが起こる。In FIG. 3, a solution 2 consisting of heavy water and an alkali halide such as lithium chloride is placed in a container 1, and a platinum electrode 3 is placed in a container 1.
and palladium electrodes 4 are arranged and connected to the anode and cathode of a power source 5 to supply power. The piezoelectric vibrator 6 is adhesively attached to the outer wall of the container 1, and the piezoelectric vibrator 6 is electrically connected to a piezoelectric vibrator power source 7. Here, when the piezoelectric vibrator power source 7 is turned on, the piezoelectric vibrator 6 starts vibrating. The piezoelectric vibrator 6. When a strong ultrasonic wave is generated, the palladium electrode 4 attached to the focal point of the ultrasonic wave also vibrates ultrasonically at the same time, and strong cavitation occurs on the surface of the palladium electrode 4.
この強力なキャビテーションにより，該パラジウム電極
４の表面では、非常に大きな圧力と、高温度の状態とな
る。そのため，該パラジウム電極４の表面での重水素の
凝集反応が急激に進む。ここで、電源５のスイッチを入
れると同時に，重水の溶液２は電気分解を開始し、重水
素は、パラジウム？ｔｔ極４の表面に集まる。その時パ
ラジウム電極４の表面に、多量の熱量が発生する．この
機構は上記の通りである。Due to this strong cavitation, the surface of the palladium electrode 4 is under extremely high pressure and high temperature. Therefore, the aggregation reaction of deuterium on the surface of the palladium electrode 4 rapidly progresses. Here, as soon as the power supply 5 is turned on, the heavy water solution 2 starts electrolyzing, and the deuterium becomes palladium? It gathers on the surface of the tt pole 4. At this time, a large amount of heat is generated on the surface of the palladium electrode 4. This mechanism is as described above.
なお、上記パラジウム電極を振動させるために用いた振
動子は，圧電振動子に限定されず、磁歪型振動子でもよ
く、また、該振動子の取り付け位置も，上記実施例に限
定されず、容器の底部分でもよい。また，該多孔質構造
パラジウム電極の粒径及び孔の形状は特に限定されない
。Note that the vibrator used to vibrate the palladium electrode is not limited to a piezoelectric vibrator, and may be a magnetostrictive vibrator, and the mounting position of the vibrator is not limited to the above example, but may be attached to a container. The bottom part of the Furthermore, the particle size and pore shape of the porous palladium electrode are not particularly limited.
（発明の効果）
本発明は，上記実施例から明らかなように、このように
構成したエネルギー発生装置は簡単な構成でかつ多量の
エネルギーを発生し得るものを提供できるため、産業上
極めて大きな効果を有する．(Effects of the Invention) As is clear from the above-mentioned embodiments, the present invention has an extremely large industrial effect because the energy generating device configured in this way has a simple configuration and can generate a large amount of energy. has.
第１図は本発明の一実施例におけるエネルギー発生装置
の概略図、第２図は本発明の実施例における多孔質構造
パラジウム電極の断面図，第３図は本発明の他の実施例
におけるエネルギー発生装置の概略図である．
工 ・・・容器， ２ ・・・重水及びアルカリハライ
ド等から成る溶液、 ３ ・・・白金電極，４ ・・・
パラジウム電極、 ５ ・・・電源、６・・・圧電振動
子、 ７・・・圧電振動子用電源、ｌ１・・・多孔質構
造表面。FIG. 1 is a schematic diagram of an energy generating device according to an embodiment of the present invention, FIG. 2 is a cross-sectional view of a porous structure palladium electrode according to an embodiment of the present invention, and FIG. 3 is an energy generating device according to another embodiment of the present invention. It is a schematic diagram of the generator. ... Container, 2 ... Solution consisting of heavy water and alkali halide, etc., 3 ... Platinum electrode, 4 ...
Palladium electrode, 5... Power source, 6... Piezoelectric vibrator, 7... Power source for piezoelectric vibrator, l1... Porous structure surface.
Claims (6)
し、前記白金電極を陽極、前記パラジウム電極を陰極と
したエネルギー発生装置において、前記パラジウム電極
として多孔質構造のものを用い、前記パラジウム電極を
振動させて成ることを特徴とするエネルギー発生装置。(1) An energy generating device comprising heavy water, a platinum electrode, a palladium electrode, and a power source, with the platinum electrode as an anode and the palladium electrode as a cathode, in which the palladium electrode has a porous structure, and the palladium An energy generating device characterized by vibrating electrodes.
し、前記白金電極を陽極、前記パラジウム電極を陰極と
したエネルギー発生装置において、前記パラジウム電極
として多孔質構造のものを用い、前記パラジウム電極を
超音波振動させて成ることを特徴とするエネルギー発生
装置。(2) An energy generating device comprising heavy water, a platinum electrode, a palladium electrode, and a power source, with the platinum electrode as an anode and the palladium electrode as a cathode, in which the palladium electrode has a porous structure, and the palladium An energy generating device characterized by ultrasonic vibration of an electrode.
し、前記白金電極を陽極、前記パラジウム電極を陰極と
したエネルギー発生装置において、前記パラジウム電極
として多結晶焼結体で構成された多孔質構造を用い、前
記多孔質構造パラジウム電極を超音波によりキャビテー
ションを発生させる構造として成ることを特徴とするエ
ネルギー発生装置。(3) An energy generation device comprising heavy water, a platinum electrode, a palladium electrode, and a power source, with the platinum electrode as an anode and the palladium electrode as a cathode, wherein the palladium electrode is a porous structure made of a polycrystalline sintered body. An energy generating device characterized in that the porous palladium electrode is configured to generate cavitation using ultrasonic waves.
窒素雰囲気中、１３００〜１６００℃で焼結形成したも
のであることを特徴とする請求項（１）、（２）または
（３）記載のエネルギー発生装置。(4) The porous structure palladium electrode is formed by sintering palladium powder at 1300 to 1600°C in a nitrogen atmosphere. Generator.
は、０．１〜１００ミクロンの範囲にあることを特徴と
する請求項（１）、（２）または（３）記載のエネルギ
ー発生装置。(5) The energy generating device according to claim 1, (2) or (3), wherein the porous structure palladium electrode has an average palladium particle diameter in the range of 0.1 to 100 microns.
５００ミクロンの範囲にあることを特徴とする請求項（
１）、（２）または（３）記載のエネルギー発生装置。(6) The porous structure palladium electrode has an average pore diameter of 0.1 to
Claims characterized in that it is in the range of 500 microns (
1), (2) or (3).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1187531A JPH0353195A (en) | 1989-07-21 | 1989-07-21 | Energy generator |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1187531A JPH0353195A (en) | 1989-07-21 | 1989-07-21 | Energy generator |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0353195A true JPH0353195A (en) | 1991-03-07 |
Family
ID=16207716
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1187531A Pending JPH0353195A (en) | 1989-07-21 | 1989-07-21 | Energy generator |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0353195A (en) |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993014503A1 (en) * | 1992-01-10 | 1993-07-22 | Chlorine Engineers Corp., Ltd. | Energy generating method based on gravitational collapse |
| WO1995016995A1 (en) * | 1993-12-03 | 1995-06-22 | E-Quest Sciences | Method for producing heat |
| WO1995023413A1 (en) * | 1994-02-23 | 1995-08-31 | The Regents Of The University Of California | Converting acoustic energy into useful other energy forms |
| WO1996041361A3 (en) * | 1995-06-06 | 1997-02-06 | Andre Jouanneau | Method and apparatus for producing and using plasma |
| WO2001039199A2 (en) * | 1999-11-24 | 2001-05-31 | Impulse Devices, Inc. | Enhancing electrolytic cavitation reactions |
| 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 |
| WO2001039198A3 (en) * | 1999-11-24 | 2002-09-26 | Impulse Devices Inc | Cavitation nuclear reactor system |
| WO2001039200A3 (en) * | 1999-11-24 | 2002-09-26 | Impulse Devices Inc | Cavitation nuclear reactor |
| WO2001039197A3 (en) * | 1999-11-24 | 2003-02-20 | Impulse Devices Inc | Cavitation nuclear reactor |
| WO2001039203A3 (en) * | 1999-11-24 | 2003-02-20 | Impulse Devices Inc | Cavitation nuclear reactor |
| KR20030033421A (en) * | 2001-10-22 | 2003-05-01 | 주식회사 미래소재 | Electrodeposition Apparatus and Method Using the Ultrasonic Wave |
| EP1376611A2 (en) * | 1995-06-06 | 2004-01-02 | André Jouanneau | Method and apparatus for producing and using plasma |
| WO2009072063A1 (en) * | 2007-12-05 | 2009-06-11 | Kimberly-Clark Worldwide, Inc. | Ultrasonic treatment chamber for initiating thermonuclear fusion |
| ITRM20080448A1 (en) * | 2008-08-08 | 2010-02-09 | Enea Ente Nuove Tec | MATERIAL TO BE USED FOR THE PRODUCTION OF EXCESS POWER, WITH HIGH LOADING OF HYDROGEN ISOTOPES, AND RELATIVE PRODUCTION PROCEDURE. |
| US8858892B2 (en) | 2007-12-21 | 2014-10-14 | Kimberly-Clark Worldwide, Inc. | Liquid treatment system |
| US9283188B2 (en) | 2006-09-08 | 2016-03-15 | Kimberly-Clark Worldwide, Inc. | Delivery systems for delivering functional compounds to substrates and processes of using the same |
| US9421504B2 (en) | 2007-12-28 | 2016-08-23 | Kimberly-Clark Worldwide, Inc. | Ultrasonic treatment chamber for preparing emulsions |
-
1989
- 1989-07-21 JP JP1187531A patent/JPH0353195A/en active Pending
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993014503A1 (en) * | 1992-01-10 | 1993-07-22 | Chlorine Engineers Corp., Ltd. | Energy generating method based on gravitational collapse |
| WO1995016995A1 (en) * | 1993-12-03 | 1995-06-22 | E-Quest Sciences | Method for producing heat |
| AU688475B2 (en) * | 1993-12-03 | 1998-03-12 | E-Quest Sciences | Method for producing heat |
| WO1995023413A1 (en) * | 1994-02-23 | 1995-08-31 | The Regents Of The University Of California | Converting acoustic energy into useful other energy forms |
| US5659173A (en) * | 1994-02-23 | 1997-08-19 | The Regents Of The University Of California | Converting acoustic energy into useful other energy forms |
| EP1376611A2 (en) * | 1995-06-06 | 2004-01-02 | André Jouanneau | Method and apparatus for producing and using plasma |
| WO1996041361A3 (en) * | 1995-06-06 | 1997-02-06 | Andre Jouanneau | Method and apparatus for producing and using plasma |
| EP1376611A3 (en) * | 1995-06-06 | 2007-09-12 | André Jouanneau | Method and apparatus for producing and using plasma |
| WO2001039199A2 (en) * | 1999-11-24 | 2001-05-31 | Impulse Devices, Inc. | Enhancing electrolytic cavitation reactions |
| WO2001039203A3 (en) * | 1999-11-24 | 2003-02-20 | Impulse Devices Inc | Cavitation nuclear reactor |
| WO2001039198A3 (en) * | 1999-11-24 | 2002-09-26 | Impulse Devices Inc | Cavitation nuclear reactor system |
| WO2001039200A3 (en) * | 1999-11-24 | 2002-09-26 | Impulse Devices Inc | Cavitation nuclear reactor |
| 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 |
| WO2001039197A3 (en) * | 1999-11-24 | 2003-02-20 | Impulse Devices Inc | Cavitation nuclear reactor |
| WO2001039199A3 (en) * | 1999-11-24 | 2002-07-18 | Impulse Devices Inc | Enhancing electrolytic cavitation reactions |
| 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 |
| KR20030033421A (en) * | 2001-10-22 | 2003-05-01 | 주식회사 미래소재 | Electrodeposition Apparatus and Method Using the Ultrasonic Wave |
| US9283188B2 (en) | 2006-09-08 | 2016-03-15 | Kimberly-Clark Worldwide, Inc. | Delivery systems for delivering functional compounds to substrates and processes of using the same |
| WO2009072063A1 (en) * | 2007-12-05 | 2009-06-11 | Kimberly-Clark Worldwide, Inc. | Ultrasonic treatment chamber for initiating thermonuclear fusion |
| US8858892B2 (en) | 2007-12-21 | 2014-10-14 | Kimberly-Clark Worldwide, Inc. | Liquid treatment system |
| US9421504B2 (en) | 2007-12-28 | 2016-08-23 | Kimberly-Clark Worldwide, Inc. | Ultrasonic treatment chamber for preparing emulsions |
| ITRM20080448A1 (en) * | 2008-08-08 | 2010-02-09 | Enea Ente Nuove Tec | MATERIAL TO BE USED FOR THE PRODUCTION OF EXCESS POWER, WITH HIGH LOADING OF HYDROGEN ISOTOPES, AND RELATIVE PRODUCTION PROCEDURE. |
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