axil - yes.  In my younger wilder days I had envisioned just that. (high temps 
with high temp alloys) Using such things at W in the alloying of Ni or Pd and 
the use of very high temps with electrically driven deuterium plasma. I even 
submitted a patent appl. for it 
(http://www.google.com/patents/WO1990014668A2?cl=en  notice that was  April 
'89)   Don't laugh too much. I was excited at the time and working on a rocket 
program at the time.
 
I still think that (high temp) is the way to ultimately go.  However, for now I 
am trying for a standalone demo and that just about requires working at lower 
temps, if it is to be self heating.  The other path would involve energy 
conversion and much more involved systems.   I am content, for now, to just 
have my sample warmer than the control.  Less heat to be sure, but fewer things 
for people to question.  My next step will to get that working temp down nearer 
to room temp.  The problem I am facing on that path is a good variable heat 
path to balance the rate of heat extraction and maintaining a significant 
sample temperature. 

 I will not be making direct claims of power yields at NI since that would 
require lengthy calibration.  I will just make the claim that the sample is 
warmer than the control and leave it at that.   But, my Ni demo should be at 
around 1 watt out with no input (but in a 80C bath) for the 5 days of expo set 
up.  Internal volume 450ml, sample mass of 200 g but that is mostly C with only 
about 2% being metal.  Perhaps someone here would like to figure how long I 
would need to run a sealed brass sphere to rule out chemistry from 4 g of 
active material  or even 200 grams total material.  (note: I have run these for 
multiple months in the lab- one set has clocked 3 months)
 
D2
 
Date: Sat, 27 Jul 2013 12:09:08 -0400
Subject: Re: [Vo]:Kitamura much improved
From: [email protected]
To: [email protected]



Comparisons
of systems are valuable in understanding what the LENR reaction is doing. As a
general principle, phonon driven dipole oscillations of electrons and
associated ions (Holes) are the power plant that drives the LENR process. 


 


Heat pumps
energy into these dipoles so that they vibrate vigorously. There is an energy
concentration mechanism that is fed by these dipoles. This concentration
mechanism absorbs this dipole energy and saves it with little or no loss in
power.  As heat is added to the system,
thermal power is transferred optically to the energy storage mechanism in the
way that a battery stores current chemically or a Cyclotron stores electrons
magnetically.


 


There is a
limit to this energy transfer mechanism but that limit is a timeframe not a
breakout of an energy containment mechanism.


 


The Cravens
system uses low quality heat to drive the LENR process. The initiation
temperature is low but the thermal power mechanism to energy accumulation is
proportionally weak because the weak flow of energy to storage is cut off by
the reaction timeframe limitation.


 


In the Ni/H
system, the initiation temperature is higher and the thermal power mechanism to
energy accumulation is proportionally stronger because the stronger flow of
energy to storage is large during  the
reaction timeframe.


 


So a high
initiation temperature makes for a stronger reaction with greater power
production.


 


As a
example of this concept, if the Creavens system increased the Debye temperature
of its material, and the bath used to supply thermal input power were hotter,
more power might be produced.


 


If a liquid
metal bath could heat the pure nickel reaction powder to high temperatures were
to replace the water bath, and nickel was used to replace the palladium alloy,
more heat output density might result.


 


Taking this
line of thinking to its extreme, the materials with the highest Debye
temperatures :( Silicon, 645K), (Beryllium, 1440 K), (Carbon, 2230 K) may
provide the most output power density. 


 


 


PS. If NASA
is using carbon nanotubes in there process, they will not reach the light off
temperatures needed for a carbon based system because that extreme temperature
is too high for standard engineering designs.     


 


 


 




On Sat, Jul 27, 2013 at 10:42 AM, Jed Rothwell <[email protected]> wrote:

DJ Cravens <[email protected]> wrote:

 
sounds like the Les Case system I have now.   Tube in a tube.
I think it is just a sensor mounted on the outside of a copper tube. The oil 
flows through the tube. Not having a T will reduce the likelihood of a leak. 
McKubre and I have some concerns about mixing. Not many concerns, because the 
calibration looks good.


   The problem is if you have the delta T too high the properties of the oil 
(heat cap., viscosity,...) start to confuse things.----- at least for me.



Yes. They have thought about these issues.

blaze spinnaker <[email protected]> wrote:


 I read 195 watts input, up to 20 watts excess.   Is that correct?



You may be right. I don't have access to the slides or abstract. 


That's a little weak and seems subject to measurement error.

It sounds like a small percent of input but I do not think it is a problem 
because the input power is direct current resistance heating. It is only needed 
to bring the cell up to the working temperature. It does not contribute 
directly to the reaction. It does not control the reaction the way Rossi's heat 
does, or Defkalion's sparking does.


DC power is very stable and easy to measure with high precision. If this were 
195 W of electrolysis, sparking or glow discharge the input power would be 
irregular and somewhat difficult to measure, but 195 W of DC power has to be 
the easiest thing in experimental science to measure. So the background noise 
is low. Having said that, from Kitamura's lecture and slides it is a little 
unclear what the background noise level is. Unclear to me, anyway.


- Jed


                                          

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