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304) Recent representative messages
Ludwik Kowalski; 7/19/2006
Department of Mathematical Sciences
Montclair State University, Upper Montclair, NJ, 07043
What follows are recent Internet messages posted on the CMNS discussion list. The debate started in 1989 is going on. On what basis are the authors
of these messages accused of being pseudo-scientists? In my opinion their methods of validation are 100% scientific. They perform experiments, they
discuss results and they develop theories, like in other areas of physical science. But our scientific establishment is practicing an unfair
discrimination against the CMNS field. When will this end?
1) Yes, knowing the weight of every substance, before and after a COP test, would be highly desirable. But I would not do this without help from a
competent, and well equipped, analytical chemist.
2) What did Fleischmann and Pons know about each chemical substance appearing and disappearing in their setup? Did they measure masses of these
substances before and after excess heat experiments? Did those who validated their excess heat conclusions, for example, Longchamps et al., determine
contributions of chemical reactions to excess heat? If so then I would very much appreciate a reference, or several references.
3) My impression, based on reading what others wrote about F&P, was that chemical contributions to excess heat was shown by them to be negligible,
a very small fraction of one percent. But I was not able to find a paper describing this. Does it exists or everyone simply assumes that it exists?
Ed Storms (E.S.) (7/18/06):
Bockris published a paper addressing this concern. As any chemist can demonstrate, the components in a F-P cell cannot produce
energy, they can only consume it because everything is in its lowest chemical state.
L.K. (not posted)
The reference given was a paper published by Kainthla et al. (in Hydrogen Energy,14, #11, 771; 1989). Bockris was listed as the last of eight authors.
The title of the paper was "Eight chemical explanations of the Fleischmann-Pons effect." Here is how the issue was discussed by Ed Storms
in review published in 2000. The title of the review was A Critical Evaluation of the Pons-Fleischmann Effect; it can be downloaded from
the library at <www.lenr-canr.org>.
In the section entitled question 2.2, Ed wrote: Can prosaic sources of chemical
energy be ruled out? The hard-to-accept claim for a nuclear source is based, in part, on the belief that observed energy production exceeds any known
chemical source. Therefore, the potential chemical sources must be examined. Before discussing this subject in detail, the reader should realize that
a typical cell contains very few chemical components, all of which are stable with respect to each other. A chemical reaction can only be initiated
by applying an electric current, a process which uses energy. Only after the water has been split into deuterium and oxygen can chemical reactions
occur. This process causes several chemical reactions, including an uptake of deuterium by the palladium and slow deposition of lithium and platinum
on the cathode surface. Each of these reactions involve very little energy. Strain energy accumulates in the palladium and small amounts of reaction
products such as D2O2 can accumulate in the solution under proper conditions.
These processes have the potential to store energy within the cell. Only release of stored energy can be used to explain the anomalous energy, which
appears after many hours of electrolysis. The magnitude of such processes was addressed in several papers. Kainthla et al. discussed eight
possible sources, including recombination, which has been already discussed above. The other sources are the energetics of PdD formation, the
energetics of PdLi formation, and energy accumulation as stress. Each of these was found to be much too small to account for even the smallest
reported excess energy. Handel proposed that heat could be pumped into the cell by a temperature gradient operating between the anode and cathode
lead wires, i.e. a Peltier Effect. Two problems exist with this explanation. A significant temperature difference seldom exists between the
two lead wires and the necessary difference between the Peltier coefficients of the wires must be unreasonably large to produce an observable effect.
Most people use platinum for both wires, which would have a zero difference in the Peltier coefficient.
Balej and Divisek compiled all necessary thermochemical values and calculated the energy involved in electrolytic formation of b-PdD. Measured
energy using inert palladium is consistent with these values, as is true of all negative studies. Berlouis et al. reported a direct
measurement of the heat of dissociation of PdH0.9, formed by electrolysis, using thermal analytical techniques. The result is consistent with values
obtained by using other techniques. Consequently, no anomalies have been found in the energetics of b-PdD. However, it is possible for an unknown
compound to form which, when decomposed, could give off the observed energy. While such a compound has been sought, it has not been detected. In
addition, such a material would have to be able to store hundreds of megajoules of energy in the few grams of palladium normally used. If this were
the energy source, the material would have an energy density greater than the most powerful chemical explosive.
11) Kainthla, R.C., et al., Eight chemical explanations of the Fleischmann-Pons effect. J. Hydrogen Energy, 1989. 14(11): p. 771.
12) McKubre, M.C.H., et al., Development of Advanced Concepts for Nuclear Processes in Deuterated Metals. 1994, EPRI.
Bockris is a highly respected electrochemist. I will accept his testimony (that the F&P excess heat could not be attributed to chemical reactions)
on the basis of authority. Ed wrote that chemical composition of F&P cells is always the same. That is why other researchers took the initial
findings for granted. Here is what I found about the above reference 12. According <www.tvwiki.tv/wiki/Cold_fusion>
McKubre et al.  have conducted careful inventories of chemical fuel and potential storage mechanisms in cold fusion cells, and they have found
neither fuel nor spent ash that could account for more than a tiny fraction of the excess heat. That is also reassuring. Mike McKubre is
one of those researchers whose excess heat data, in F&P type cells were highly reproducible at levels below 2 W.
Post Scriptum: Referring to the above quote from the wikipedia, Mike McKubre wrote: On several occasions we did find and reported
(at ICCF8 and elsewhere) a nuclear "ash" quantitatively (and temporally) correlated to the excess heat - Helium-4.Ê With regard to chemical "ash" our
statement is actually stronger than the one written above.Ê We never saw any evidence of any net chemical reaction accompanying excess heat production.Ê
The statement of less than 1 part in 100 (or 1000) refers to any conceivable chemical reaction of the cell constituents - no matter how unlikely
5) Generally speaking, one can identify two ways of dealing with the issue of what is going on in a F&P cell. Let me name them negative
and positive. The negative approach, suggested by Peter and Michel, (see unit #303) is one of them. The best one can do with
that approach is to produce convincing data that excess heat is not due to a well known chemical process. Thepositive approach would be
to show that excess energy can be explained by a particular kind of a process, for example, fusion producing neutrons, protons, tritons and helium-3.
What must be done, experimentally, to convince ourselves that excess heat is indeed due to emission of such particles? One must show that the total
number of nuclear particles, and their energies, match the measured amounts of excess heat.
Many attempts in that direction have been made in the past but they were not successful. Excess heat was always found to be zillions of time larger
than what could be made consistent with observed emission of neutrons, protons, tritons and 3He. Another particular
process that was investigated was cold fusion in which dominant products are atoms of 4He. Such process is extremely
rare in hot fusion (collisions of isolated deuterons) but that does not mean that it must also be rare in cold fusion (where deuterons are not isolated).
I know that accumulation of 4He has been studied by many researchers and that the rate of accumulation of excess heat (about 24 MeV per atom of
4He) was found to be consistent with the expectation. It is well known that the mass-energy of two deuterons exceeds
the mass-energy of one 4He by 23.8 MeV.
In my opinion the positive approach -- showing that excess energy measured matches amount of ashes (products of specific
processes) is likely to convince mainstream scientists that something unexpected is going on, than the negative approach suggested by Peter
and Michel. People who studied accumulation of 4He reported high reproducibility of results. Taking this for granted,
I would recommend (if it were up to me) the following approach. Select five recognized experts in 4He detection and ask
them to replicate already reported results. If at least one of them confirms the ~24 MeV of excess heat per one 4He
atom then it would be reasonable to assume that the effect deserves further investigations. My expectation is that all five experts would report
proportionality between accumulated excess heat and accumulated 4He ash. The energies per atom would probably be
different, for example, ranging between 15 and 35 MeV.
Even 5 MeV per atom of an ash would be six orders of magnitude higher than what is possible with a chemical reaction. But what would one have to say
if reproducible results were 1 to 5 MeV per atom? That would tell us that 4He is not produced via direct fusion of
two deuterons. We would say that another nuclear process, or a sequence of processes, is involved. How else can atoms of a new chemical element be
Accumulation of 4He was one of the three categories of topics identified for the 2004 DOE review. The panel of
appointed experts was asked about production of 4He as an ash associated with this excess heat, in amounts
commensurate with a reaction mechanism consistent with D+D --> 4He + 23.8 MeV (heat). Unfortunately, not a
single reexamination request was made by the DOE. What they did was to collect comments from experts who were asked to read existing reports. I was
very disappointed by this. Here is how comments made by the appointed experts were summarized in the DOE report:
The hypothesis that excess energy production in electrolytic cells is due to low energy nuclear reactions was tested in some experiments by
looking for D + D fusion reaction products, in particular 4He normally produced in about 1 in 10,000,000 in hot D + D
fusion reactions. Results reported in the review document purported to show that 4He was detected in five out of sixteen
cases where electrolytic cells were reported to be producing excess heat. The detected 4He was typically very close to,
but reportedly above background levels. This evidence was taken as convincing or somewhat convincing by some reviewers; for others the lack of
consistency was an indication that the overall hypothesis was not justified. Contamination of apparatus or samples by air containing
4He was cited as one possible cause for false positive results in some measurements. Why was a reexamination of the effect
not ordered by the DOE after some of the panel experts reported that the evidence was convincing?
Jacques Dufour (J.D.). . . the worst of our enemies is ourselves. We think our experiments
perfect, we are sure that we have answered theoretically all the questions. This is very far to be true. Submitting the work you do to critics and
having the lucidity to accept remarks when they are valuable is essential. It is a great error not to seak interaction with people on the ground that
they are our enemies and that we don't have to take into account their advices. . . .
I agree with Jacques on a few of his points. Of course talking with people who do not yet accept cold fusion is important.
It is essential to understand just what they lack to allow them to arrive at a rational conclusion. We are long past the situation where the reality
of cold fusion is in doubt. Too many of the required questions have been answered and too many studies from which the main errors have been removed
have been reported. I'm in the process of examining this literature in detail for a book, so I can say with confidence that the claims are true. I'm
also aware that most people who do not believe are simply ignorant of this extensive literature, as are many people in the field.
Consequently, when dealing with skeptics, you have to realize you are dealing with someone who has a very limited and selective knowledge. Their
attitude of rejecting what you say because you are a believer, hence can not be trusted, is totally illogical. All scientists have basic beliefs
based on what they have been taught or have observed in nature. These beliefs do not make them untrustworthy when describing the evidence for these
beliefs. . . . The challenge now is to evaluate what is real and what is not real in an effort to understand just how the effect works. We have a
mixture of good and bad work, and a mixture of bits and pieces of the total puzzle. The challenge is to sort this collection into pieces that make
sense and can advance our understanding about how the amazing process works.
Michel Jullian (M.J.):
Ed to reconcile your two statements above, there must be at least one experiment of which you are 100% sure, which one
Well, aside from my own work :-), I pick the McKubre heat measurements, the Iwamura transmutation studies, the Miles
helium studies, and the Claytor tritium studies. I pick these because the work is so well done and described to allow critical evaluation. Many other
studies would be considered very good once the CF phenomenon is accepted. All of the radiation studies are important because it is impossible to miss
radiation and none should be produced by the low energy CF cells. All of the neutron measurements are useless and irrelevant to the issue. In addition,
185 credible heat measurements, 58 reports of significant tritium, and 67 studies of transmutation are published. Any other field of study would be
embarrassed to have rejected this much work by well known and competent scientists.
. . . I have tried to pass the message that the most important thing in the field was the heat measurement and that the interpretation would come later.
But every body sticks to the nuclear interpretation.
All of the methods are difficult to make work every time. When the effect is made to occur and the experiment is well designed,
any of the methods would be accepted by normal scientists. However, some methods are more complex than the others, the Mizuno method for example.
Consequently, this method is more difficult to demonstrate, as you are discovering. The best method is to design a good calorimeter that you can
demonstrate is accurate, use it to measure heat by the classic F-P approach, and measure another expected nuclear product at the same time - helium or
radiation for example. If you can show a one-one correlation between heat and another nuclear product, the work gains in credibility, but also gains in
difficulty. I suggest, no matter how well you do the Mizuno experiment, the apparatus will be too complex to convince the average person. The work
needs to be understandable by an average 10 year old for many people in physics to believe the results.
. . . I suppose that many of the 185 heat measurements, mentioned by Ed, were in electrolytic cells similar to those used by Fleischmann and Pons.
As far as I know, excess heat, in highly reproducible experiments, was most often generated at rates below two watts. Is this correct? And the emphasis
was to show that excess heat was not an illusion due to experimental errors.
What I would like to see are reports claiming that excess heat was extraordinary. That is the most interesting (and most controversial) part, as far as
science is concerned. Like Jacques, I am willing to wait for convincing demonstration that the measured excess heat is nuclear. Showing that it cannot
be explained by prosaic effects would already by a big step forward. I am taking it for granted that calorimetry was essentially error-free, and that
electric energy supplied to cells was measured properly. But how did the authors of reports convince themselves, and others, that their highly reproducible
results could not be attributed to a chemical reaction? Which reports are the most convincing in that respect?
Ludwik, I disagree with your comment that calorimetry and input power measurement can be trusted and only chemical heat should
be distrusted, we must check carefully every single possible artefact, or the house of cards falls down. . . .
1) Nothing should be trusted in a single report. But tens of highly qualified scientists reported positive excess heat results. That is why I am confident
that excess heat, generated at the rates below 2 W, is not an illusion due to experimental error. Experimental errors would produce as many positive as
negative results. My impression was that results above 2 W are not yet reproducible in F&P cells. Please correct me if I am wrong.
1) That is correct. [many of the 185 heat measurements, were in electrolytic cells similar to those used by Fleischmann and Pons].
However, several other methods have been used including low energy plasma and exposure of the NAE [nuclear active environment] to ambient gas pressure.
2) [Ludwik wrote]: As far as I know, excess heat, in highly reproducible experiments, was most often generated at rates
below two watts. Is this correct? And the emphasis was to show that excess heat was not an illusion due to experimental errors.
A wide range of maximum heating power has been reported. However, the results can only be properly evaluated when the expected
error is included. For example, excess power of 5 mW is reported, but this was obtained using a calorimeter accurate to a microwatt. The issue is not the
amount of power, because this is determined by the amount of NAE present. The interesting result is how the NAE can be produced.
3) If you study the Miles work about the He-heat relationship and add the 6 other studies that agree with his results, you will see that a nuclear reaction
has to be the explanation.
4) Not every study can prove the results are not chemical or are even caused by a nuclear reaction. However, if someone does an experiment and gets the
same anomalous result as someone who has shown their anomalous results to have a nuclear source, it is reasonable to conclude that you both are seeing
the same phenomenon. After all, when chemists study a chemical reaction, they are not required to prove each time the existence of atoms or the laws of
thermodynamics. At some point, people acknowledge the reality of the underlying process.
1) I suppose that demonstrating the non-chemical origin of excess heat generated at the rate of 5 mW would be much more difficult than at 1000 mW.
2) In an earlier message you wrote: "Two issues exist that are frequently confused. The first is whether an anomalous effect
has actually been observed. . . . The second issue is the process causing the anomalous behaviors." That is true. I am familiar with many
reports describing anomalous effects; emission of charged particles and Iwamura's transmutations are good examples. My question was about something very
different. I asked for chemical data supporting the anomalous nature of excess heat generated in highly reproducible experiments, such as those reported
by McKubre. As I wrote before, I believe that reality of excess heat was demonstrated in these experiments. But what was done to show that excess heat
measured could not be attributed to prosaic effects?
3) You also mentioned anomalous helium demonstrated by Miles, and by other researchers. Generation of 4He at the rate of about one atom per 24 MeV of
excess heat is indeed a very convincing argument that a nuclear process was taking place. You are correct that this automatically rules out chemical
explanations. Even ten times lower rate would exceed the expected chemical rate by six orders of magnitude (MeV versus eV). I wish we were sufficiently
equipped to demonstrate the unusually high rate of accumulation of reaction products in Colorado2. But we were not. The only method available to us, if
we want to demonstrate the anomalous nature of excess heat, is chemical analysis of reaction products, as argued by Peter Gluck. Our manuscript would have
no chance of being published without an appendix with arguments against trivial origin of excess heat. Do you agree?
1) . . . all of the F-P cells use the same material, the same chemical arguments apply to all of them, as above.
2) [Concerning our manuscript would have no chance of being published . . ] The Mizuno cell is more complex chemically than the F-P cell.
Consequently, it requires more discussion. As I suggested before, the best defense is to prevent anything from leaving or entering the cell. This way,
chemical effects can be easily ruled out.
Mitchell Swartz (M.S.):
Referring to F&P cells Ed wrote that everything is in its lowest chemical state. Actually this is not correct.
There is energy given off by the loading of palladium by the deuterons which we have been measuring for years with our sensitive calorimeters. That
heat given off with loading ranges from circa 50 to several hundred joules or so, but in any case the heat given off is DWARFED by both the excess
energy during the experiment and the "heat after death" (when the systems are correctly operated at their optimal operating points), and is
recovered when deloading occurs. However, this demonstrates that they are not in their "lowest chemical state" at t=0+.
Also, since the Gibbs free energy involves BOTH enthalpy and entropy, I do not believe all other materials are in their lowest chemical state during
the run. For example, I reported that both gold, palladium, and platinum anodes decompose very slightly producing an overlay on the cathode which
is capable of, in some cases of palladium with heavy water (and certain other cases) of producing slight excess heat (as I discussed at LENR-2 Texas,
which you attended, and thereafter termed "crud"). FWIW that slight excess heat is DWARFED by the excess heat achieved when the reactions
are correctly carried out.
In addition, there appear contamination issues arising from the containers (etc.) which are an entropic effect also demonstrating that the systems
are not in their "lowest chemical state". However, again, although the contamination markedly lowers the excess heat, as we demonstrated
at ICCF-10 (2), and although the energy involved is DWARFED by the excess heat achieved when the reactions are correctly carried out, it is not
strictly accurate to make the claim that all materials are in their "lowest chemical state" at t=0+.
The bottom line is that careful calorimetry with full controls, waveform reconstruction, and time integration, and with monitoring of loading
energy, etc. is required to prove excess heat. Handwaving alone is probably not sufficient.
Dr. Mitchell Swartz
(1) Swartz, M., "Possible Deuterium Production From Light
Water Excess Enthalpy Experiments using Nickel Cathodes",
Journal of New Energy, 3, 68-80 (1996)
(2) Swartz. M., G. Verner, "Excess Heat from Low Electrical
Conductivity Heavy Water Spiral-Wound in D2O/Pt and
Pd/D2O-PdCl2/Pt Devices", ICCF-10 (Camb. MA),
Proceedings of ICCF-10, (2003).
Cold Fusion Times http://world.std.com/~mica/cft.html
The journal of the scientific aspects of loading isotopic fuels
into materials ISSN# 1072-2874
JET Energy http://world.std.com/~mica/jet.html
Working for Safe and More Efficient Heat Products to Serve You
Actually, formation of PdD produces energy but the need to decompose D2O to get the deuterium results in a loss of energy, i.e. the
net effect is an endothermic reaction.
. . . We don't need tens nor thousands of experiments, we need a single one that anyone could trust 100%, agreed? Do we have it?
Actually, five criteria determine what is accepted as reality in science.
1. As you say, a perfect experiment would be nice. Unfortunately these are very rare in all fields of science. Clever people can always imagine alternative
explanations. Nevertheless, we have several that are close.
2. A collection of measurements that all show the same patterns of behavior. For example, everyone who makes the necessary measurements sees that greater
heat is associated with a greater D/Pd ratio.
3. Finding measurements that give values in agreement with other independent studies. For example, the measured He atom/watt-sec agrees with energy values
calculated from mass defect.
4. The measurement agrees with accepted theory.
5. 100% reproducibility is possible.
Criteria #2 and #3 have been met by several different types of behavior. We are working toward the last two. No observation ever starts out meeting all
five criteria, yet novel observations are frequently accepted and studied until all five criteria are met. Why should cold fusion be different?
. . . Fleischmann's papers show no evidence of analytical studies of reactants and all products (before versus after). Was such analysis perform for at
least one McKubre's experiment ? You referred to them as highly reliable. Perhaps Mike will tell us something about this.
Mike McKubre (M.M.):
Our experiments were designed so that the issue of potential chemical energy sources could be very easily bounded and a complete (or
sufficient) chemical balance was attained in every case of reported excess heat. I discussed this many times in tedious detail in 1989-92 but let me
The SRI heat producing cells were thermodynamically closed, physically sealed, and contained only Pt (anode and wiring), Pd (cathode), D2O + LI (electrolyte),
fused silica and PTFE (walls and inner construction). Sometimes there were known trace additions of deliberate additives (most commonly Al and Si,
occasionally B and Be - the last I would not advise). The recombiner catalyst was Pt (or Pd) on alumina. Cells were precharged with D2 gas in
an amount calculated to leave a positive gas pressure (sometimes large - mostly small) after full D/Pd loading.
It is standard calorimetric procedure to ensure that final state = initial state. This was done by deloading the Pd and checking that the electrolyte
concentration (directly reflected in the conductivity) is the same at the end as the beginning. With these constraints it is easy to show that the
sum of all chemical reactions is VERY small compared to the two elephants: the integrated input IV and any excess heat. I have often stated publicly
that the ratio of excess energy we observed to the sum of all conceivable chemical sources is 100 - 1000 (or more). A shorthand way of
understanding this is that we have measured excess energy corresponding to more than 1000 eV / Pd atom* [footnote below].
Both Ed & Mitch have spoken about the transient enthalpy of D loading (then unloading) in Pd. In our scheme the net enthalpy in both directions
is very nearly zero. When D is derived from D2 the loading process is at first exothermic (the partial molar enthalpy negative). That is, the
D prefers to be inside the Pd until a loading of D/Pd~0.725 (I am working from memory here). At this point the sign reverses and it becomes
increasingly more difficult (endothermic) to insert each D atom** [second footnote]. At a loading D/Pd ~ 0.95 (or maybe a little higher) the integral
enthalpy is zero. Independent of sign the one way enthalpy is (as Mitch stated) DWARFED by input and excess enthalpies. In the method that Ed
described where cells do not operate with excess D2, all loaded D must come from D2O (H2O) and Ed is correct that the net enthalpy of D (and H) absorption
is always negative.
Each experiment needs to be evaluated separately and no general rule should be assumed to apply. Even as (presumably) competent electrochemists with
colleagues who are (presumably) competent analytical chemists we chose at the outset to make our lives easier by designing simple experiments with
few moving (i.e. reacting) parts. The analytical difficulties of open cells, particularly those designed (or permitted) to have carbonate electrolytes
are much more severe. Without direct experience I don't feel qualified to discuss them.
* Our maximum is >2000 eV per Pd atom - Energetics have recorded over twice this number.
** This was a point discussed by Fleischmann & Preparata at ICCF5
Could we try and concentrate the _whole group_'s brain power on achieving 1/, see if together with all the collective know-how and
creativity and mutual criticism we are capable of unleashing we can design this irrefutable excess heat experiment we all need? It seems to me we already
have some great building blocks waiting to be assembled.
Ok, depending on the original contributions which will be actually used (which can only be determined when the job's done) the author list may end up
several tens of names long (alphabetical order obviously), and the Nobel prize podium may be overcrowded, so what?
The problem with your idea, Michel, is that two problems need to be solved. One problem is to design an experiment without significant
error. This is the problem you are addressing and the one that can be and has been largely solved. The other problem is the creation of the nuclear active
environment. This is presently produced by nature when she is in a good mood, which is not very often. No one knows how to make this material on purpose,
although some methods are more successful than others. Anyone who figures this out will have caught the brass ring and will obtain a patent before discussing
the method. Consequently, your suggestion will not be followed.
1) I still think that this "irrefutable excess heat experiment" might be based on a Mizuno-type cell. Why? Because 50-100 W is very impressive.
The most challenging task, for the moment, is to convince ourselves, and others, that excess heat cannot possibly be due to well known chemical reactions.
2) I would be happy to see Mizuno alone on that podium. Or Fleischmann+ Pons, or anyone else who made an essential contribution. The most important thing
is to end the unjustified discrimination against the CMNS field. We are not pseudo-scientists; our motivation is to contribute to scientific and technological
I too think the magnitude of the effect makes GDPE the best candidate, but Ed doesn't, mainly because, as often discussed here, it is
difficult/dangerous to close the system as would be required for a total chemical balance. . . .
Michel, I have been designing experiments in an attempt to eliminate significant error for the last 17 years in this field. I have designed and built most
of the calorimeter types used in this field. Even if I say so myself, I probably know more about calorimeter error than anyone in the field, except perhaps
Mike McKubre. I now have two very sensitive and very error-free Seebeck calorimeters. So, your suggestion has been implemented. The problem is to find a
sample that actually makes heat.
L.K (not posted).;
Why is this a problem? If I had a working F&P-type cell I would certainly bring it to you. Most researchers would probably be very happy to cooperate
1) [L.K., referring to W/cm^3] asked: Does this mean that arguments presented by Bockris
and his coworkers (in the paper you recommended) should now be rejected? The use of the term W/cm3 and the Bockris arguments
have no relationship to each other. W/cm3 is a method to normalize the power to the volume of the sample, as I said. The Bockris arguments apply to the
energy being produced by chemical processes.
2) [L.K. wrote about eV/atom.] . . . The ratio turns out to be much larger than 1000 eV/atom. What is wrong with saying "a chemical
reaction cannot possibly produce such result?"
You are assuming there is a relationship between the amount of metal removed from the cathode and the amount of energy produced. In
fact, the energy was produced by a nuclear reaction and material was lost by a chemical-mechanical process that is completely independent of the nuclear
reaction. The absolute amount of energy is the only important value.
1) OK, I understand E.S.. Division by a constant number does not change the ratio of two heats (chemical/excess). The answer is in the ratio, not in power
2) Concerning The absolute amount of energy is the only important value. That depends on the context. My purpose
was to rule out a possibility that excess heat might be chemical. In that context I assumed that tungsten is a chemical fuel. This assumption cannot
possibly be defended because the eV/atom are too high. What is wrong with this method of reasoning? Yes, I know the same should be done for any other
chemical substance whose mass was reduced considerably during the experiment. Chemists in Paris will probably do this. I suspect that eV per atom of
consumed potassium would also not be consistent that K is a chemical fuel. W and K are probably the only substances whose masses are reduced significantly
when excess heat is measured. But that must be verified by chemists. Our Colorado2 appendix would be sufficiently convincing if masses lost are determined
and if eV/atom are shown to be excessive for every potential chemical fuel. Will this be done in Fauvarque's lab? I hope so.
Gentlemen, there is obviously something wrong in your calculation of the energy of reaction per atom. I assume the cathode is
palladium (atomic weight : 106,42). So the number of mole involved is 5/106,42 = 0,047 mole. This gives an enthalpy of reaction of some
50000/0,047 = 1064000 J/mole (1064 kJ/mole which is close to the upper limit for chemical reactions). If you want the figure in eV per atom,
then number of atom 0,047*6*1E23 = 2.82*1E23. Energy en eV = 50000/1.6*1E-19 Hence energy in eV per atom : 11,08 eV.
I wrote: ". . . Assume that 15 grams of the cathodic metal is found at the bottom of the cell. That would mean that only 5 grams of the cathode
reacted. " I have no idea how much metallic W was really found at the bottom of the cell by Pierre. 5 grams was purely hypothetical. I am sorry
for not making this clear. The only numerical calculation performed was 20-15=5. The rest was speculation.
If 5 grams leads to 11 eV/atom, as calculated by Jacques, then 0.05 grams would lead to 1100 eV/atom. According to Mizuno, if my memory can be trusted,
99.99% of lost tungsten was recovered as metal, at the bottom of the cell. The number 1000 eV/atom was posted by Mike; that is why I wrote that 1000
eV/atom would be highly convincing. The main point was to show that we do have ammunition to argue that the COP = 1.24 was not due to chemical processes.
It is a matter of measuring, or estimating, masses of lost chemical substances. I hope this path will be followed.
Ludwik Kowalski wrote: That depends on the context. My purpose was to rule out a possibility that excess heat might
be chemical. Yes, I understand the purpose. You need to show that the TOTAL amount of energy
is greater than the sum TOTAL of all possible chemical reactions producing heat. This means you need to identify all chemical reactants and products, and
determine their quantity. This is relatively easy because only a few reactants are present and their reaction products are well known, or at least can be
easily determined. You don't even need to speculate about what is made. This is normal, well understood chemistry. Forget about eV/atom. This has no
meaning unless it is associated with a demonstrated chemical reaction. For example, you might make a little WO3 and when this is divided into a lot of
heat the result is a big ev/atom value for that particular ratio. But this means nothing because the actual heat producing reaction might generate many
atoms you have not identified.
L.K. (not posted):
I still think that the only chemical substances to be considered, for the eV/atom, are those that were present before the experiment, and whose
masses were reduced considerably. The WO3 is the intermediate product. But all this makes sense only in the context of
ruling out chemical origin of excess heat. Heats of combustion of most fuels are below 5 eV per atom, or per molecule. That is why numbers like
1000 eV/at should be convincing.
Let me show another exchange of messages that appeared on the CMNS yesterday. They show that list members are aware of people who might be tempted
to exploit the existing controversy and promote nonscientific agendas. Most CMNS researchers do not want to be associated with such agendas.
Am I the only person to receive this message? It came this morning.
Glad to see your article. Now we have some news and I hope you'll be interested. Our web site is <http://www.faraday.ru>
Moller and Naudin are wrong way. Best regards, Alexander V. Frolov Faraday Lab Ltd.
Who is Frolov? I do not remember communicating with him before. But I clicked on the above link and read about two commercially available products.
Very impressive, if true. Comments and information will be appreciated.
I heard of Frolov in the field of "Lifters" (there was talk of a "Frolov hat" device supposedly
exhibiting "reactionless" forces or something of the kind), as far as I can tell he is at least as much "wrong way" as
the competitors he denigrates. I suggest to wait until he actually delivers what he promises before buying any "fuel less" electricity
generator from him :) You could also try a Google search . . .
William Beaty (W.B.):
A. Frolov is a longtime member of the fringe science community. In Russia in ?1996? he organized a conference on CF,
antigravity, "torsion" and other fringe physics. My overall impression: he is not a scientist, he lacks the brutal self-honesty
Re. the products. The one on the left looks suspiciously like the "Potapov device," a water heater based upon a pump driven by
an electric motor. It was claimed to put out more thermal watts than the motor watts input. Potapov brought one to the USA for informal
testing, and it only gave normal results with no anomalous excess output. Yet his company was selling them in Russia without being able
to support their claims that it was better than a simple electric water heater. We never decided if Potapov was running a scam, or if he'd
fallen into "pathological science" and was honestly fooling himself. And that Frolov is selling a perhaps-fradulent device
doesn't surprise me. . . .
This website contains other cold fusion items.
Click to see the list of links