On August 14 and 15, 2020 the 12th Conference on Free Energy COFE convened on ZOOM.
This is a transcript of the talk by Dr. Edmund Storms Cold Fusion: From Rejection as Fiasco to being Salvation of Civilization.
The rejection is continuing but the salvation has yet to start. To understand the fiasco, a little history is required.
Cold Fusion was born on March 23, 1989
Fathers: Martin Fleischmann, Prof. University of Southampton, Fellow of the Royal Society (born 1927, died 2012)
Stanley Pons, Prof. University of Utah, Chairman of the Chemistry Department (born 1943, now living in France)
Mother: Curiosity and Luck
Cold Fusion was discovered by Professors Martin Fleishmann and Stanley Pons working at the University of Utah and announced in 1989. This was a BIG DEAL. Their discovery was announced around the world. Everyone realized the importance. People predicted that the pollution being caused by oil extraction and transport could be eliminated. Nuclear accidents would no longer be a worry. We now know that if this clean energy had been developed 31 years ago, future global warming would have been reduced. As result, the rejection has had serious consequences to the future of civilization.
Fleischmann, M.; Pons, S.; Hawkins, M. Electrochemically induced nuclear fusion of deuterium. J. Electroanal. Chem. 1989, 261, 301.
I was working at LANL (Los Alamos National Laboratory) at the time. The laboratory was attempting to develop fission power for use in space, which is a very difficult problem. In fact, having sufficient power for extended space travel is still a problem. The power produced by cold fusion could be the ideal solution. As result, people at Los Alamos became very exited. Dozens of people stopped their normal work and attempted to replicate what Fleischmann and Pons claimed. I was able to make tritium and then excess energy using their method. Both studies were published in a peer reviewed scientific journal.
Storms, E. K.; Talcott, C. L. Electrolytic tritium production. Fusion Technol. 1990, 17, 680.
Storms, E. K. Measurements of excess heat from a Pons-Fleischmann-type electrolytic cell using palladium sheet. Fusion Technol. 1993, 23, 230
Response of the Scientific Community
LANL/DOE Workshop of Cold Fusion Phenomenon, Santa Fe NM May 23-25, 1989
NSF/EPRI Workshop on Anomalous Effects in Deuterated Metals, Washington D.C. October 16-18, 1989
A workshop was held in Santa Fe in May for interested people from all over the US and from several other countries to plan how best to study cold fusion. Another larger workshop was held in Washington in October. There some of the results were discussed. As you can see, the scientific community was mobilizing to investigate this unusual nuclear process.
As expected, many efforts failed and many people were skeptical of the claim – for good reason. Nevertheless, work was underway with an open mind to determine what was real and what was not.
Response of the US Government
But then people involved in the extraction and use of oil took notice. They realized they would be put out of business if cold fusion were made useful. In addition, people who were trying to harness fusion using a different and more complex method, called hot fusion, realized they might suffer the same fate. So, H. W. Bush, an oil-man and president at the time, asked the DOE (Department of Energy) to look into the reality of the claim.
First review was in November 1989, called the Energy Research Advisory Board, Cold Fusion Panel.
A committee was assembled of about 22 people, most who had no understanding of the subject and no interest, but had important positions. The co-chairman, John Huizenga, ran the show and wrote the report. When the other co-chairman, Norman Ramsey, read the report, he was appalled by the obvious bias and threatened to resign if changes were not made. The changes were made but had no effect on how the report was understood by everyone.
This review sets the tone for the rejection that continues to this day.
ERAB “Report of the cold fusion panel to the Energy Research Advisory Board,” Department of Energy, DOE/S-0073, 1989
As a result, all work sponsored by the US government stopped as did some work in other countries. As a Japanese scientist told me, if the US DOE says the effect is nonsense, it must be nonsense. That confidence in the opinion of the DOE no longer exists. Work in Japan and in other countries is now underway. Eventual success by these efforts could result in a national security threat to the US. Once again, the rejection by the DOE could have serious future consequences.
Iwamura, Y.; Itoh, T.; Kasagi, J.; Kitamura, A.; Takahashi, A.; Takahashi, K.; Seto, R.; Hatano, T.; Hioki, T.; Motohiro, T.et al. Anomalous Heat Effects Induced by Metal Nano-composites and Hydrogen Gas. J. Cond. Matter. Nucl. Sci. 2019, 29, 119.
Kitamura, A.; Takahashi, A.; Takahashi, K.; Seto, R.; Hatano, T.; Iwamura, Y.; Itoh, T.; Kasagi, J.; Nakamura, M.; Uchimura, M.et al. Excess heat evolution from nanocomposite samples under exposure to hydrogen isotope gases. International J. Hydrogen Energy 2018, 43, 16187.
Iwamura_, Y.; Itohy, T.; Kasagi, J.; Kitamuraz, A.; Takahashi, A.; Takahashi, K. Replication Experiments at Tohoku University on Anomalous Heat Generation Using Nickel-based Binary Nanocomposites and Hydrogen Isotope Gas. JCMNS 2017, 24, 191.
The rejection was so strong and nasty that Pons and family immigrated to France and became French citizens. He and Fleischmann continued their studies there with support from a Japanese company.
Fleischmann, M. Reflections on the sociology of science and social responsibility in science, in relationship to cold fusion. Accountability Res. 2000, 8, 19.
In order to remove any doubt about his opinions, Prof. Huizenga wrote a book entitled “Cold Fusion: The Scientific Fiasco of the Century”. Little did he know at the time the book its self would be the fiasco.
Huizenga, J. R. Cold fusion: The scientific fiasco of the century; second ed.; Oxford University Press: New York, 1993.
The orchestrated and sometimes nasty rejection slowed work but it did not stop it. Many wealthy individuals took notice, realized the importance to mankind, and the profit potential. Also, people like myself who saw the effect continued their studies. In my case, I was able to continue my studies at Los Alamos for another year because the laboratory administration realized the reality and the importance of the discovery even if the DOE did not. I retired after the DOE clamped down on even this small effort.
My wife and I moved to Santa Fe where we built a house with an attached wood-working workshopcold fusion laboratory combination. I continued my studies with support from people who understood the importance of the discovery. Over the years I wrote two books, 10 reviews, close to 100 published papers, and have done experiments involving all aspects of the process. I can say with certainty based on personal experience and on a complete examination of available information, the claimed discovery is real!
Storms, E. A New Source of Energy using Low-Energy Fusion of Hydrogen. Environmental Science : An Indian Journal 2017, 13 (2), 1.
Storms, E. The Present Status of Cold Fusion and its Expected Influence on Science and Technology Innovative Energy Policies 2015, 4 (1).
Storms, E. K. A Students Guide to Cold Fusion, www.LENR.org, 2012.
Storms, E. K. The status of cold fusion (2010). Naturwissenschaften 2010, 97, 861.
Now that 31 years have passed during which thousands of studies have been done in laboratories in at least 12 countries, let’s see what the evidence shows.
What the Science Shows Us
Let’s look first at energy production. The energy is measured as power, i.e. watts, using a calorimeter. Many possible errors have been identified and are now avoided. The so-called excess power cannot result from a prosaic process such as a chemical reaction because the required chemicals are not present or because the magnitude far exceeds any possible chemical reaction.
Histogram of Power Produced by 157 Studies using Pd-D (1989-2006) (Batch sensitive)
This figure shows a histogram in which the number of independent measurements is compared to the power being measured. The excess power is produced by small samples of palladium (about several grams) electrolyzed in D2O. This pattern has continued up to the present time.
Storms, E. Anomalous Energy Produced by PdD. J. Cond. Matter. Nucl. Sci. 2016, 20, 81.
Azizi, O.; El-Boher, A.; He, J.-H.; Hubler, G. K.; Pease, D.; Isaacson, W.; Violante, V.; Gangopadhyay, S. Progress towards understanding anomalous heat effect in metal deuterides. Current Science 2015, 108 (4), 565.
As you can see, most studies report less than a few watts, but a significant number are able to produce much more power. The amount depends on the nature of the Pd, not on its physical form or the treatment. If a piece of Pd is found to produce the effect, most samples taken from that batch will be active. Unfortunately, most batches of Pd are not active. The reason for this difference is only now being understood. As result, the effect can now be produced with much greater confidence.
What kind of nuclear reaction might be the source of the energy?? The only kind of fusion known before cold fusion was the so-called hot fusion. It is called hot because the deuteron must be raise to a very high temperature for fusion to take place, in this case, in plasma. The He4 that results is unstable and fragments two ways, one produces tritium plus a proton and the other produces a neutron plus He3.
Because the neutron is easy to detect, it was one of the first nuclear products sought as a test of the cold fusion claim. No neutrons were detected no matter how hard people looked. The skeptics then used the mantra, “no neutrons, no fusion”.
Nevertheless, tritium was produced and clearly detected. How could tritium be made without neutrons? This question was never answered which allowed the skeptics to ignore this contradiction.
Production of He4 without fragmentation was suggested. This reaction would produce 23.85 MeV of energy. This idea was shot down because the required energetic and deadly gamma emission was clearly not produced. There were no dead graduate students and Fleischmann and Pons were healthy. Besides, momentum could not be conserved without this deadly radiation being emitted, which meant that the helium could not result from fusion. The detected He4 could even be conveniently explained as an air leak because air contains 5.25 ppm of helium.
Morrey, J. R.; Caffee, M. W.; Farrar IV, H.; Hoffman, N. J.; Hudson, G. B.; Jones, R. H.; Kurz, M. D.; Lupton, J.; Oliver, B. M.; Ruiz, B. V.et al. Measurements of helium in electrolyzed palladium. Fusion Technol. 1990, 18, 659.
Nevertheless, people were seeing evidence for He4. The first person to accurately measure the relationship between helium and energy production was Dr. Melvin Miles working at the Naval research center in China Lake. I will show his results later but first let’s look a more recent study with an interesting back-story.
Bush, B. F.; Lagowski, J. J.; Miles, M. H.; Ostrom, G. S. Helium production during the electrolysis of D2O in cold fusion experiments. J. Electroanal. Chem. 1991, 304, 271.
Miles, M.; Bush, B. F.; Ostrom, G. S.; Lagowski, J. J. Second Annual Conference on Cold Fusion, “The Science of Cold Fusion”, Como, Italy, 1991; p 363.
Miles, M. H.; Hollins, R. A.; Bush, B. F.; Lagowski, J. J.; Miles, R. E. Correlation of excess power and helium production during D2O and H2O electrolysis using palladium cathodes. J. Electroanal. Chem. 1993, 346, 99.
Miles, M.; Bush, B. F.; Lagowski, J. J. Anomalous effects involving excess power, radiation, and helium production during D2O electrolysis using palladium cathodes. Fusion Technol. 1994, 25, 478.
Les Case was a catalyst chemist who had the idea that a chemical catalyst might initiate the cold fusion process. So, he had friends at United Catalyst prepare a typical catalyst with palladium on charcoal. Gradually they discovered how to make excess energy and helium. Les was looking forward to making money by using the free energy to purify sea-water that he would use to irrigate barren land in Australia. He would then make his money selling the land, thus avoiding all the problems associated with the reputation of cold fusion.
He ordered a large batch of the catalyst. Much to his dismay, the material was dead. The reason was soon discovered. During a clean up, the company had thrown away the barrel of charcoal being used to make his material. This was special charcoal made from coconuts grown on an island in the Pacific. Apparently, the many extra elements in this material were important.
Case, L. The 9th International Conference on Cold Fusion, Condensed Matter Nuclear Science, Tsinghua Univ., Beijing, China, 2002; p 22.
Case, L. C. The Seventh International Conference on Cold Fusion, Vancouver, Canada, 1998; p 48.
Case, L. C. The reality of ‘cold fusion’. Fusion Technol. 1991, 20, 478.
Case, L. COPRODUCTION OF ENERGY AND HELIUM FROM D2, WO 97/43768, USA, 1997.
Meanwhile, Les had sent some of the active material to Michael McKubre at SRI for him to test. Mike had a very high-resolution mass spectrometer that allowed him to measure He4 in the presence of D2 gas. Mike designed a calorimeter that allowed him to measure excess power and helium at the same time while the material was heated at 250° C in D2 gas, according to Les’s instructions. The graph on the right shows how the excess energy and helium increased over a 20 day period. Note the reaction was slow to start and then became more rapid.
The graph on the left shows the relationship between helium and excess energy. As you can see, the values all fall on the same straight line even after the helium content in the gas exceeded the concentration in air. Consequently, the helium did not come from air. Also, the straight line has a slope consistent with the energy/He4 ratio produced by the D+D fusion reaction.
McKubre, M. C. H. Tenth International Conference on Cold Fusion, Cambridge, MA, 2003. 16
McKubre, M. C. 14th International Conference on Condensed Matter Nuclear Science, Washington DC, 2008; p 673.
McKubre, M. C.; Tanzella, F. Cold fusion, LENR, CMNS, FPE: One perspective on the state of the science based on measurements made at SRI. J. Cond. Matter Nucl. Sci. 2011, 4, 32.
If the values obtain by Miles are combined with three other independent studies that also used the electrolytic method to react Pd with D2O, this relationship is produced. The distribution of values shows the average He/energy ratio is nearly equal to ½ of the value expected if the reaction were D+D=He4. This difference is expected because only the helium in the evolving gas was measured. Some helium would have remained in the Pd metal, which was not measured.
Nevertheless, the agreement between the measurement and the required value is close enough to make this behavior the smoking gun.
Besides, the shape of the distribution is consistent with a normal Gaussian error function. In other words, the measurements are consistent with the occurrence of the same nuclear reaction having an expected amount of random error. Such consistency could not result from only experimental error.
Gozzi, D.; Caputo, R.; Cignini, P. L.; Tomellini, M.; Gigli, G.; Balducci, G.; Cisbani, E.; Frullani, S.; Garibaldi, F.; Jodice, M.et al. Fourth International Conference on Cold Fusion, Lahaina, Maui, 1993; p 6.
Bush, B. F.; Lagowski, J. J. The Seventh International Conference on Cold Fusion, Vancouver, Canada, 1998; p 38.
DeNinno, A.; Frattolillo, A.; Rizzo, A.; Del Gindice, E. Tenth International Conference on Cold Fusion, Cambridge, MA, 2003; p 133.
DeNinno, A.; Frattolillo, A.; Rizzo, A.; Del Giudice, E. In ASTI-5; www.iscmns.org/: Asti, Italy, 2004.
Miles, M. Tenth International Conference on Cold Fusion, Cambridge, MA, 2003; p 123.
Tritium is another nuclear product that should not be produced according to the skeptics. Here are two examples of tritium being made by two different methods used at LANL. Dozens of other examples have been reported by other laboratories.
Storms, E. K. The science of low energy nuclear reaction; World Scientific: Singapore, 2007.
Tom Claytor subjected a small cathode of various alloys to low-voltage gas discharge while measuring the tritium in real time in the circulating D2 gas. The voltage is too small to produce the hot fusion reaction as he determined by the absence of measured neutrons. You can see an example of what happens when no plasma is present and when a dead alloy is used. The active alloy clearly produced tritium. He tested dozens of alloys and found some made much more tritium than others. Again the reaction was batch dependent. Tom continued his work at LANL until the DOE forced him to stop. He then set up a private laboratory near his home where he continued to study this and other methods to cause the cold fusion reaction.
Claytor, T. N.; Fowler, M. M. In 12th International Workshop on Anomalies in Hydrogen Loaded Metals Italy, 2017.
Claytor, T. N.; Fowler, M. M.; Storms, E. K.; Cantwell, R. In Space Technology & Applications International Forum Albuquerque NM, 2016
Claytor, T. N.; Schwab, M. J.; Thoma, D. J.; Teter, D. F.; Tuggle, D. G. The Seventh International Conference on Cold Fusion, Vancouver, Canada, 1998; p 88.
Claytor, T. N.; Jackson, D. D.; Tuggle, D. G. Tritium production from a low voltage deuterium discharge of palladium and other metals. J. New Energy 1996, 1 (1), 111.
Claytor, T. N.; Jackson, D. D.; Tuggle, D. G. Tritium production from low voltage deuterium discharge on palladium and other metals. Infinite Energy 1996, 2 (7), 39.
Claytor, T. N.; Tuggle, D. G.; Taylor, S. F. Third International Conference on Cold Fusion, “Frontiers of Cold Fusion”, Nagoya Japan, 1992; p 217.
The other graph compares two cells that Carol Talcott, later to become Carol Storms, studied at LANL using the electrolytic method. Two identical cells were run at the same time in the same location, with one making tritium and the other not. The study was able to show the tritium was not initially in the Pd and did not come from the environment. Production of tritium was delayed for 3 days, continued for about 20 days then stopped. This behavior is typical of all of the many published reports of tritium production.
Storms, E. K.; Talcott, C. L. Electrolytic tritium production. Fusion Technol. 1990, 17, 680.
Packham, N. J. C.; Wolf, K. L.; Wass, J. C.; Kainthla, R. C.; Bockris, J. O. M. Production of tritium from D2O electrolysis at a palladium cathode. J. Electroanal. Chem. 1989, 270, 451.
Hodko, D.; Bockris, J. Possible excess tritium production on Pd codeposited with deuterium. J. Electroanal. Chem. 1993, 353, 33.
Iyengar, P. K.; Srinivasan, M.; Sikka, S. K.; Shyam, A.; Chitra, V.; Kulkarni, L. V.; Rout, R. K.; Krishnan, M. S.; Malhotra, S. K.; Gaonkar, D. G.et al. Bhabha Atomic Research Centre studies on cold fusion. Fusion Technol. 1990, 18, 32.
When tritium (T) and neutrons (n) are measured at the same time, a rough correlation is found that centers on a T/n ratio of about 106. This is shown using a histogram of the number of independent measurements plotted against the log of the T/n ratio. The value produced by the hot fusion process can be seen on the left.
Srinivasan, M. Observation of neutrons and tritium in the early BARC cold fusion experiments. Current Science 2015, 108 (4), 619.
In other words, although the ratio does not match the value produced by hot fusion, neutrons seem to result from a process influenced by the tritium content. This behavior adds one more clue about the nature of the fusion process.
Several studies show that tritium production requires a mixture of D and H. However, if these two isotopes were to fuse, He3 would be the expected product. Tritium would result only if an electron were added during the process. So, we apparently have another clue about the nature of the fusion process.
Romodanov, V. A.; Savin, V. I.; Skuratnik, Y. B.; Majorov, V. N. Sixth International Conference on Cold Fusion, Progress in New Hydrogen Energy, Lake Toya, Hokkaido, Japan, 1996; p 340.
Claytor, T. N.; Fowler, M. M. In 12th International Workshop on Anomalies in Hydrogen Loaded Metals Italy, 2017.
And now the plot thickens and tests whether you actually have an open mind. The process has been found by many people to produce what is called transmutation. This is a reaction during which one or more hydrogen nuclei are added to other elements, thereby causing production of a new element. Such reactions are even more difficult to justify and explain than fusion because of the huge Coulomb barrier. Apparently, fusion must occur in order to provide the energy and fusion product that is then added to a nearby nucleus. We will see more evidence for this conclusion shortly.
This figure shows one kind of transmutation reaction that results in addition of several D to Pd or Pt followed by fission of the product to produce two smaller nuclei. These two smaller nuclei result in the two populations you can see on the left. This behavior implies that the fusion process can involve atoms that happen to be near where fusion is taking place. In addition, the resulting nuclear reaction can be novel and unexpected.
Srinivasan, M.; Miley, G.; Storms, E. K. In Nuclear Energy Encyclopedia: Science, Technology, and Applications; Krivit, S.;Lehr, J. H.;Kingery, T. B., Eds.; John Wiley & Sons: Hoboken, NJ, 2011.
Miley, G.; Shrestha, P. In ACS Symposium Series 998, Low-Energy Nuclear Reactions Sourcebook; Marwan, J.;Krivit, S. B., Eds.; American Chemical Society: Washington, DC, 2008.
But the plot thickens even more. Researchers at Mitsubishi Heavy Industries in Japan explored transmutation using a sandwich of CaO (calcium oxide) and Pd (palladium). You can see a magnified cross-section on the right. When they caused D2 gas to diffuse through this layer, excess energy was produced. Even more amazing, when they deposited various elements on the exposed Pd surface, these were transmuted in unexpected ways.
Iwamura, Y.; Itoh, T.; Yamazaki, N.; Yonemura, H.; Fukutani, K.; Sekiba, D. Recent advances in deuterium permeation transmutation experiments. J. Cond. Matter Nucl. Sci. 2013, 10, 63.
Iwamura, Y.; itoh, T.; Terada, Y.; Ishikawa, T. Transmutation reactions induced by deuterium permeation through nano-structured Pd multilayer thin film. Trans. Amer. Nucl. Soc. 2012, 107, 422.
Iwamura, Y.; Itoh, T.; Yamazaki, N.; Kasagi, J.; Terada, Y.; Ishikawa, T.; Sekiba, D.; Yonemura, H.; Fukutani, K. Observation of low energy nuclear transmutation reactions induced by deuterium permeation through multilayer Pd and CaO thin film. J. Cond. Matter Nucl. Sci. 2011, 4, 132.
Iwamura, Y.; Sakano, M.; Itoh, T. Elemental analysis of Pd complexes: effects of D2 gas permeation. Jpn. J. Appl. Phys. A 2002, 41 (7), 4642.
Iwamura, Y.; Itoh, T.; Gotoh, N.; Toyoda, I. Detection of anomalous elements, X- ray, and excess heat in a D2-Pd system and its interpretation by the electron-Induced nuclear reaction model. Fusion Technol. 1998, 33, 476.
Their initial study involved applying cesium to the Pd surface by vapor deposition. They found that praseodymium was produced. Using in-situ XPS (X-ray Photoelectron Spectroscopy), they were able to show that the cesium concentration decreased as the amount of praseodymium increased. No other nuclear products were detected.
Apparently, two He4 or four D enter the nucleus of cesium all at the same time. Attempts to replicate the claim at NRL (Naval Research Laboratory) failed but were successful at another independent laboratory in Japan. This work has continued and the claims have become even better supported by the evidence. Then they deposited other elements with the results shown in the table. Apparently, as many as three He4 nuclei can be added simultaneously to another nearby nucleus, with the number depending on the nature of target element. Once again, we are given clues about the very strange mechanism causing cold fusion. Once again we are forced to consider the impossible.
But Nature is not finished with producing amazing behavior. For many years, various studies have suggested that living cells can also produce transmutation. Naturally, this claim was soundly rejected.
Kervran, C. L. Transmutations biologiques, metabolismes aberrants de l’asote, le potassium et le magnesium. Librairie Maloine S. A, Paris 1963.
Komaki, H. Production de proteins par 29 souches de microorganismes et augmentation du potassium en milieu de culture sodique sans potassium. Revue de Pathologie Comparee 1967, 67, 213.
Kervran, C. L. Biological transmutations; Swan House Publishing Co., 1972.
Biberian, J.-P. Biological transmutations. Current Science 2015, 108 (4), 633.
Nevertheless, workers in Ukraine decided to explore this idea. They used a well-known kind of yeast as the living cell, to which they added D2O and manganese 55. The intent was to determine if iron 57 would be produced. They used the Mossbauer effect to detect the iron 57 isotope.
In case you are not familiar with this method, when Fe57 results from k-capture (an electron from the k electron shell enters the nucleus) of Co57, which is a conventional nuclear reaction, the resulting gamma can be absorbed by another Fe57 nucleus if the energy state of the target atom exactly matches the energy of the gamma. The energy of the gamma is matched to the absorbing Fe57 energy-state by changing the relative velocity between the emitter and the target atom.
The figures show the amount of adsorption as the relative velocity is changed. The graph on the left shows no reduction in gamma intensity when H2O is used and when manganese is absent. When manganese and D2O are both present, the gamma is absorbed, which shows that Fe57 was produced. Eventually, they were able to make the process very robust, with the result shown on the right. Clearly, a deuteron can be added to a manganese nucleus to produce iron 57. Nothing else would result in absorption of the radiation.
You might ask why the yeast would want to make iron out of manganese. I will leave this question as a homework assignment.
Vysotskii, V.; Kornilova, A. A. Low-energy nuclear reactions and transmutation of stable and radioactive isotopes in growing biological systems. J. Cond. Matter Nucl. Sci. 2011, 4, 146.
Vysotskii, V.; Tashyrev, A. B.; Kornilova, A. A. In ACS Symposium Series 998, Low-Energy Nuclear Reactions Sourcebook; Marwan, J.;Krivit, S. B., Eds.; American Chemical Society: Washington, DC, 2008.
Vysotskii, V.; Kornilova, A. A.; Samoylenko, I. I. Experimental discovery and investigation of the phenomenon of nuclear transmutation of isotopes in growing biological cultures. Infinite Energy 1996, 2 (10), 63.
Vysotskii, V.; Odintsov, A.; Pavlovich, V. N.; Tashirev, A.; Kornilova, A. A. 11th International Conference on Cold Fusion, Marseilles, France, 2004; p 530.
Now they asked, what would happen if the target isotope were radioactive? Would the transmutation reaction change the decay rate? They tested this idea by placing cesium 137, a common radioactive product of the fission reaction, in their yeast culture. They found that the effective decay rate was increased up to 35 times. The figure shows the measured reduction in activity as a function of time when other elements were added to the mixture. The designation MCT means a culture that was found to be especially active. As your can see, the presence of certain elements made the loss of Cs137 more rapid because some Cs was transmuted to a 30 stable element, thereby making less Cs available to decay. An obvious use would be to accelerate the natural decontamination at Chernobyl.
Vysotskii, V. I.; Kornilova, A. A. Microbial transmutation of Cs-137 and LENR in growing biological systems. Current Science 2015, 108 (4), 636.
Vysotskii, V.; Kornilova, A. A. Nuclear fusion and transmutation of isotopes in biological systems; MIR Publishing House, Russia 302, 2003.
Up to now, I have avoided discussing the radiation that must result from the nuclear process in order for the energy to be dissipated and turned into heat in the calorimeter. The radiation is also required to conserve momentum. Once again, the cold fusion process confounds explanation because very little radiation is detected outside of the apparatus. This is good news for the health of the experimenter but bad news for the effort to understand the process. What is worse, the radiation that is detected is highly variable and sometimes very unusual. Consequently, this question is too complex to answer here.
Nevertheless, radiation is emitted and detected, as is required. However, it does not have the large expected energy.
Now I would like to show some actual data and what it implies. Here is a plot of the log excess power vs 1/T. This is a typical Arrhenius plot that allows the activation energy for a reaction to be determined.
Storms, E. K., unpublished, 2020
The excess power was produced by a 0.5 g sample of Pd that had been activated and then reacted with deuterium at 20° C using electrolysis. Excess power was produced immediately after the Pd had reacted with deuterium and the sample was heated. The long delay experienced by other studies did not occur.
The red squares were produced while 0.1 A was applied to the cathode. This held the D/Pd ratio constant at PdD0.85. You can see that all the values fall nicely on a straight line.
The other values resulted when this current was turned off. This allowed D to be lost. The resulting D/Pd ratios measured before and after each temperature study are shown. As you can see, the excess power was not changed by the ratio changing from 0.85 to 0.46. Other studies showed no change even when the ratio was reduced to 0.16. Consequently, we can conclude that once the nuclear reaction starts, it is not influenced by the concentration of D in the material.
However, the temperature clearly has a large effect on the rate of energy production. The slope of the line between 30° and 90° C can be used to calculate an energy of activation for the rate limiting process. This activation energy is 28.7 KJ/mole. Using this value, we can determine the mechanism that limits the rate of the nuclear reaction.
Simple logic requires the deuterium that is converted to helium at a particular location to be replaced. This deuterium must come from the surrounding physical structure. The rate of transport through a structure is determined by the diffusion constant. If the log diffusion constant of D through PdD0.85 is plotted vs 1/T, the activation energy for diffusion can be determined. The activation energy for diffusion is found to be 28.0 KJ/mol. This value is consistent with the activation energy that limits the nuclear process within experimental error.
In addition, every sample studied showed the same activation energy regardless of the total amount of power being produced. Consequently, the rate of power production above about 30° C seems to be determined by how fast deuterium can diffuse through the lattice and replace D being converted to helium.
This graph also shows a change in the effect of temperature below about 30° C. I can propose an explanation for this behavior, but this would require too much time and require you to understand the mechanism I have proposed to explain all observed behavior. Unfortunately, we do not have time to discuss this idea.
Storms, E. How Basic Behavior of LENR can Guide A Search for an Explanation. JCMNS 2016, 20, 100.
Storms, E. How the explanation of LENR can be made consistent with observed behavior and natural laws. Current Science 2015, 108 (4), 531.
Storms, E. K. The explanation of low energy nuclear reaction; Infinite Energy Press: Concord, NH, 2014.
Eight general behaviors describe the behavior of the nuclear process. These behaviors can be used to prove without a doubt that nuclear reactions of several unusual kinds can take place in a chemical environment without application of enough energy to overcome the Coulomb barrier in the normal way. The behaviors can also be used to create a model to describe the process. The process is clearly very unusual and not consistent with how conventional nuclear processes are found to behave. Consequently, a new kind of nuclear interaction must be considered, instead of rejecting the evidence because it conflicts with what is known.
THE REJECTION WAS AND IS A HUGE MISTAKE!!
I can’t emphasis this enough.
Two basic facts have now been demonstrated.
A new kind of nuclear interaction can be initiated in different kinds of condensed matter, including living cells, to cause fusion of hydrogen isotopes and transmutation of other elements.
An ideal source of energy is available without the threats to the environment created by carbon containing compounds and fission of uranium.
As Arthur C. Clarke said, “Ignoring cold fusion is one of the greatest scandals in the history of science”. This comment still applies.
Clarke, A. C. 2001: The coming age of hydrogen power. Infinite Energy 1998, 4 (22), 15
The only challenge remaining is to understand the process well enough to make it useful.
I have written two books that summarize the observations and explanations. These are out of print but can be obtained from Amazon and World Scientific in digital form.
More information can be obtained from these sources.
A digital library containing many of the papers about cold fusion is administered by Jed Rothwell and is available on the Internet at http://lenr.org/
A peer-reviewed digital journal was created to make papers about cold fusion available because such papers are commonly rejected by other journals. This journal is edited by Jean-Paul Biberian and called J. Condensed Matter Nuclear Science. JCMNS now has 32 volumes.
Copies of many papers from the twenty-two ICCF conferences can be found at LENR.org.
Thank you for showing interest. I also want to thank my computer, the Internet, and the great skill and patience of Tom Valone for making this talk possible.
Copyright by Edmund Storms August 2019. May be quoted freely with attribution.
Relationship between the burnishing process used by Mizuno and the Storms theory of NAE formation [.pdf] by Edmund Storms Kiva Labs, Santa Fe, NM (8/1/19)
Mizuno  has applied Pd to Ni mesh by burnishing and claimed to make excess energy by heating the material in D2 gas. This method is expected to produce the conditions predicted by Storms to cause LENR. The relationship between the burnishing method and the Storms theory of LENR is described as well as several testable predictions.
The LENR process involves two separate and independent events, one involving a common chemical process and the other caused by a unique nuclear process. The first event creates a condition in the material in which the nuclear process can function. Without this condition being present, the nuclear process cannot take place. But once this special condition forms, the nuclear process occurs without further delay. The difficulty in causing the LENR process results from failure to create this required special condition.
According to the Storms’ theory, this special condition, called the NAE (Nuclear Active Environment), consists of physical gaps having dimensions of a few nanometers between the atomic planes. Such gaps can be formed in many different ways, but up to the present time they have resulted when stress is relieved at random sites within the physical structure. The stress is created when the material, usually palladium, reacts with isotopes of hydrogen, thereby causing expansion. Removal of the hydrogen causes contraction, during which time most of the gaps (cracks) form. This counter intuitive conclusion results because the expansion resulting during reaction with hydrogen produces mainly compressive stress, which on average would not produce gaps. Removal of hydrogen produces contraction that results in the kind of stress required to produce gaps. Consequently, according to the Storms model, the Pd must experience deloading at one time during the study for LENR to be triggered. Once formed, the NAE seems to be stable for long periods of time.
After a gap forms, generally at a grain boundary, the local stress can be relieved most easily by making the gap wider rather than by causing other gaps to form. This natural tendency causes the initial small gaps to grow wider and form what can be clearly seen as cracks rather than remain small enough to cause LENR. This process results because less energy is required to move atoms further apart once the atomic bond as been broken than is required to break the bond in the first place. Nature will always take the path of least resistance. This conventional process explains why LENR is not initiated even though many cracks are clearly observed.
The amount of overall dimensional change, hence amount of stress, is related to the amount of hydrogen that reacts, thereby causing an apparent relationship between the maximum D/Pd ratio achieved by the material and the amount of excess energy resulting from formation of numerous gaps. Although, palladium is normally used to form the required gaps, which is the example used in this paper, other materials can be expected to experience the same process and consequently produce LENR.
The greater the number of gaps having the required dimension, the greater the overall rate of LENR. Because suitable gaps are rarely produced in conventional materials, the challenge is to modify the material such that a large number of independent small gaps can form during loss of hydrogen or by other means. The application of Pd to a Ni surface by the burnishing process, as used by Mizuno, achieves this requirement in two ways.
The first requirement is achieved because Pd is applied an amorphous form. Upon reaction with hydrogen, this non-crystalline structure would convert to the fcc structure at many independent sites. We can expect the resulting stress to cause many isolated gaps to form within the Pd layer. Additional gaps (cracks) would form at the Pd-Ni interface as result of the Pd expanding more than the Ni because the Pd reacts to a much greater extent than does Ni. Of great importance is that each of these processes takes place at many independent sites, with the stress not focused on only a few sites as is normally the case.
The second requirement involves the small particles of NiO that would be removed from the Ni surface and mixed with the Pd layer. A gap would be expected to form between the surrounding Pd metal and this inert inclusion, as hydrogen is lost from the structure.
If this description were correct, it would be expected to apply to all Pd found to produce LENR. I predict that commercial Pd observed to support LENR contains similar unintended inclusions that remain in the metal after the refining process and were not altered when the metal was formed into wire or sheet. Consequently, most pieces of the batch are found to produce LENR regardless of the final form created by physical means. This behavior explains why some batches of commercial Pd produce LENR for no obvious reason.
As an example, Fleischmann has described how boron is added to the molten Pd during the purification process to remove oxygen by formation of insoluble boron oxide, which floats to the surface and is physically removed. In view of the Storms model, the small pieces of oxide scattered throughout would make the Pd eventually nuclear active rather than the absence of oxygen.
The burnishing process was explored by rubbing a Pd rod against a 1 mm thick piece of Ni (1 cm x 2 cm) that had been previously electroplated with Pd. No NiO would be expected to be present on the Ni surface. As shown in Fig. 1, the amount of Pd transferred from the rod to the Ni was a linear function of the number of strokes after the first 50 strokes. In other words, each stroke transferred the same amount of Pd. The surface acquired a smooth bright metallic appearance where the rubbing had been applied. Fig. 2 shows islands of Pd, some of which appear to be poorly attached. This sample will be studied to determine what happens during reaction with D in the absence of included NiO.
FIGURE 1. Weight gain of the Ni sheet as result of pressing the edge of a Pd rod against the surface and moving it across the full length of the Ni plate. Each stroke was made at a random location on the surface so that most of the surface was eventually burnished with Pd.
FIGURE 2. SEM picture of a surface to which Pd was applied using the burnishing method. The Ni had been previously electroplated with Pd. Notice the islands of Pd. By eye, the surface looked polished and reflective where the burnishing had been applied.
A second sample of Ni was flame heated to about 800° C to form a visible (blue color) oxide layer after which it was burnished in the same way as the first sample. Although the blue color was removed to produce a bright metallic surface, no detectable weight increase (±0.00005 g) was produced after 600 strokes. Apparently the nature of the Ni surface affects the amount of Pd transferred to the surface. Consequently, the condition of the surface is revealed as being another important variable. This condition needs to be explored.
Any material that is not firmly attached to the surface would be expected to be pushed aside by the burnishing process and not be included in the Pd layer.
These samples will be first studied using electrolytic loading to determine how the Pd layer affects the uptake of D into the Ni using methods previously described. The production of excess energy will be studied up to 85° C in D2O. If energy is detected, the samples will be studied in D2 gas up to 350°C.
Replicating exactly the procedure used by Mizuno is not as important as replicating what Mizuno caused. If he actually caused LENR, this result could be produced many different ways, as is typical of all natural phenomenon including LENR. Identifying the important variables becomes important so that the resulting LENR process can be replicated at will with total control. Some of these variables are suggested below as predictions. If these suggested methods cause LENR, this would provide further evidence that the NAE suggested by Storms is correct.
Although Storms also proposed a mechanism for the nuclear process, this part of the theory is not important when trying to create the conditions initiating the nuclear process because once the NAE forms, the nuclear process starts without any further knowledge or effort being required. Consequently, learning how to make and control the production of the NAE is the only important knowledge needed to cause and use LENR. Absence of this knowledge has been the reason for general rejection and why the various efforts have failed to make useful energy.
Use of Ni that has been slightly oxidized by being heated in air to a temperature sufficient to cause thickening of the oxide layer will be more nuclear active than clean Ni.
Use of Ni sbeet rather than a mesh will increase the effectiveness of the process by increasing the surface area of the deposited Pd.
Use of other metals that form an oxide surface layer, such as Ag, Cu, Ti, and Fe, will be suitable as a substrate to which Pd is applied.
Application of surface layers other than oxide to the substrate can be expected to improve the effectiveness of the process.
Other metals that form hydrides, such as Rh, Ti, Zr, or Hf, should cause LENR when used as the burnished material.
Use of softer alloys of Pd, such as Pd-Li, are expected to produce a more effective burnished layer compared to pure Pd. This alloy might also be more effective because it is more reactive to hydrogen than pure Pd.
Burnished Pd can be expected to produce LENR when used as the cathode during electrolysis and gas discharge, as well as when the gas loading method of Mizuno is used.