Re: [Vo]:New Arata experiment described in the lecture of May 22, 2008

2008-05-29 Thread Harry Veeder
Jed,
You may have already said this, but among the Arata peer reviewed papers on
your site, which is the most similar to the may 22 demonstration?

harry



Re: [Vo]:New Arata experiment described in the lecture of May 22, 2008

2008-05-28 Thread Jed Rothwell
Edmund Storms wrote:

Jed, what happens from 0 to 300 min?

Large heat burst during the period when the gas stream is turned on. This graph 
shows data after the gas stream is turned off, as I said in my initial messages.


 Why is this critical time missing? 

It is shown in other graphs.

Sorry but I cannot upload additional graphs at this time. It took considerable 
effort to upload this one. I have no reliable internet access, and no other 
graphs at this time. (Actually, Arata sent them but this computer does not have 
the software to read them.)


On the face of it, this graph proves nothing. It only shows that 
Pd-Zr-Ni reacts more rapidly with D2 than does ZrO2-Pd. The behavior of 
H2 is anomalous and makes no sense.

It may make more sense after you see more data. It shows a limited amount of 
excess heat from H2, and much more heat from D2. The burst of heat from both D2 
and H2 is in other graphs, as I said. Arata assumes the H2 heat burst is 
entirely chemical.

Please reserve judgment. I regret my inability to communicate.

- Jed





Re: [Vo]:New Arata experiment described in the lecture of May 22, 2008

2008-05-28 Thread Jed Rothwell
I think Ed meant to send this response to Vortex, but it came to me because of 
the peculiar on-line reader I use. Anyway, let me respond here:

Edmund Storms wrote:

Jed, let me describe what happens when a material that is reactive with 
H2 or D2 is exposed to the gas. This description is not hypothetical but 
is based on personal observation.

As the gas is added, the sample starts to get warmer, which causes the 
reaction to increase in rate. The temperature eventually increases until 
the ambient pressure and the temperature are more or less in 
equilibrium.

. . . 

As for the behavior when H2 was used, this gas should have produced an 
initial temperature almost identical to that produced by D2.

This is exactly what Arata observed, and what he reported. That is what is 
shown in Figs. 2 and 4 that I just uploaded. The chemical reaction during the 
gas loading phase produces the same amount of heat with deuterium and hydrogen, 
using samples of ZrO2 of the same mass (7 g).


 The fact 
that it did not is very strange and suggests the data were not taken 
under the same conditions.

This is Ed's misunderstanding, caused by the fact that I sent Fig. 5B first. 
Fig. 5B shows what happens AFTER gas loading, when the effects with deuterium 
and hydrogen begin to diverge. During the initial phase the two react almost 
exactly the same way.

Question for Ed: is Arata's measurement of 4.4 kJ of chemical heat from an 18 g 
sample plausible? Too much? Too little?


In contrast, if the sample reacts easily with the gas, as is the case 
with the Pd-Ni-Zr alloy, a lot of heat is generated quickly and the 
reaction is quickly completed.

This is also exactly what Arata observed and reported.


As a result, the temperature increases 
rapidly and also decays away rapidly, as was observed. 

Arata noted this.


The only 
observation that makes the reported behavior unique is the generation of 
helium, which is not shown on the graph. 

Helium is not shown in this graph, as noted. However, it was not detected with 
hydrogen and it was with deuterium. Furthermore, there are two pronounced 
differences in the reported behavior: the heat with deuterium lasts ~3000 
minutes longer than with helium (and would probably last much longer), and the 
delta T temperature difference between the cell core and wall continues with 
deuterium, whereas it disappears with hydrogen. These are very significant and 
in my opinion, they mean there is heat production with deuterium after gas 
injection, but no heat production with hydrogen.

- Jed





Re: [Vo]:New Arata experiment described in the lecture of May 22, 2008

2008-05-25 Thread Jed Rothwell
Akito Takahashi sent some corrections to my report:

Arata did not stop D2 feeding when inside pressure came to rise up.

The High Temperature Society is Kouongakkai in Japanese. (I had it the high 
voltage society.)

Amount of helium-4 factorx10~17 corresponds to 0.5 to 1 Mega Joules, by 23.8 
MeV/He-4.

Takahashi believes The lecture could be followed completely by native Japanese
speakers but I know several who were baffled.


Additional comments from Takahashi:

The key result of Arata this time is the long lasting heat generation without 
input power, associated with helium-4 generation.

This is essential to making RD further for energy source application. (As I 
too mentioned.)

- Jed





[Vo]:New Arata experiment described in the lecture of May 22, 2008

2008-05-24 Thread Jed Rothwell
In this report, I assume the reader is familiar with Arata’s previous 
experiments. See his papers at LENR-CANR.org.

The new experiment uses a steel cell about 20 cm tall and 3 cm in diameter. (I 
do not have the dimensions in writing but I saw the cell.) A sample of 
zirconium oxide with palladium nanoparticles in (ZrO2*Pd) it is placed at the 
bottom of the cell. In some tests, an alloy of Zr*Ni*Pd is used. The cell is 
initially evacuated, and at room temperature.

Highly purified deuterium gas is pressurized in an external tank to about 100 
atm, and then injected into the cell in a high powered jet stream of gas, for 
about 10 minutes. The gas is in the jet stream is ionized and much of it is 
instantly absorbed by the material. Heat production begins immediately. The gas 
is not absorbed by the steel vessel walls.

Heat production begins with a large burst lasting as long as the gas stream is 
injected. The temperature rises to about 70°C. Arata says this is caused by a 
combination of chemical and nuclear reactions. After the gas flow is shut off, 
the cell remains warm for 50 hours, gradually cooling. It would probably remain 
significantly warm for 100 hours, although they have not continued the 
experiment this long yet. During the second phase, the temperature in the 
center of the cell remains significantly warmer than at the outer cell wall, 
typically about a half-degree Celsius. This half-degree temperature difference 
remains about the same during the 50 hours of the run.

Arata thinks that the heat from the second phase is entirely from a nuclear 
reaction. In one example, the first phase produced 4.4 kJ (at a rate of 18 
kJ/hour, or ~5 W), and the second phase produced ~250 kJ (at ~4 kJ/hour, ~1 W).

Much of the gas is absorbed by the Zr-Pd target. Gas pressure rises gradually 
after the flow is cut of, as the sample degasses.

Helium is produced in the same ratio to the heat as with plasma fusion. 
However, the Zr-Pd sample has to be baked out after the run, to recover all of 
the helium.

Three control experiments are described:

* Hydrogen with the Zr-Pd target. The cell heats up in the first phase. After 
the gas stream is turned off, it cools down. There is no significant difference 
between the cell center and outer cell wall. Arata think the heat comes 
entirely from a chemical reaction. Helium is not produced.

* Deuterium with no Zr-Pd. No heating effect or helium is observed. Gas 
pressure rises immediately in a straight line, and stops rising as soon as the 
gas flow is cut off.

* Hydrogen with no Zr-Pd. The same result as with deuterium.

Arata believes that highly pure deuterium is the key to success, and also, by 
the way, that helium contaminates the surface and must be removed in order to 
keep the reaction going.

The DS-cathode configuration outer shell acted as a hydrogen purifier. The 
disadvantage was that it had to be heated to ~200°C with an auxiliary heater to 
allow the hydrogen to pass through the shell. In the latest configuration, 
Arata dispenses with that and uses pre-purified deuterium so that the cell can 
be operated starting at room temperature, without an auxiliary heater.

The other advantage, not mentioned by Arata in this lecture, is that the 
nanoparticles of palladium do not sinter together as they did with Pd-black. 
The zirconium, which is 90% of the material, keeps them apart.

A small electric motor is placed next to the cell, and powered by a 
thermoelectric generator that when there is a large temperature difference 
between the cell and ambient. Arata neglected to describe it during the 
lecture, although it was shown in a diagram. Apparently it is a proof of 
principle device. As far as I could tell, he neglected to mention several other 
details, such as the method of calibration, and the nature of the chemical 
reaction in the first phase. His lecture was difficult to follow, even for 
native speakers, so I may have overlooked something.

Note that even without a calibration the comparison control experiments prove 
there is heat, but Arata has calculated the amount of heat (~250 kJ), so he 
must have done some sort of calibration.

The high operating temperature, instant response and reliability of this device 
make it the most practical form of cold fusion yet developed. The small amount 
of palladium is also a major advantage. As far as I know, all of the tests with 
Zr-Pd targets and D2 have produced heat immediately and predictably. It may not 
be possible to turn off the reaction instantly, but this is no impediment to 
practical applications; it is not possible to turn off the heat from burning 
coal or uranium fission either. The reaction stops gradually as the sample 
degasses. It might be possible to force it to degas more rapidly, by raising 
the temperature and pumping out the cell.

This is awkward without graphics, but to give an example of the reaction, in 
Fig. 5B (not shown here), room temperature is 24°C. A ZrO2*Pd 

Re: [Vo]:New Arata experiment described in the lecture of May 22, 2008

2008-05-24 Thread Nick Palmer
Wasn't a zirconium compound the secret sauce that the Cincinnati group 
used in their tile burn experiment (replicated by Chris Tinsley)?


Nick