From: Peter Gluck 

 

http://egooutpeters.blogspot.ro/2015/03/hardcore-lenr-palladium-still-shining.html

 

 

Palladium may be still “shining” at a few conferences, but the glow has 
tarnished considerably in the race for commercial viability. “Classic LENR” in 
general is:

1)      Low power – typically subwatt

2)      Based on electrolysis of heavy water at low temperature

3)      Poor to very poor reproducibility

4)      Expensive electrodes - $1000/gram range

5)      High COP – but only if the experiment is kept well below one watt

6)      Inverted economy of scale – lower COP at higher temperature

 

In contrast, nouveau LENR (aka dogbone) version is

1)      Three to four orders of magnitude higher power output

2)      Based on solid state -> gas phase at elevated temperature

3)      (Apparently) more reproducible, even without precisely following 
earlier work

4)      Low cost materials

5)      Modest, but usable COP

6)      Threshold for maximum gain appearing near 1300k-1400k.

 

It is easy to see why “Classic LENR” is essentially on its last legs as far as 
commercial relevance goes – and yet there are a few lessons, generally 
overlooked, which can be applied to the newer efforts.

 

Of significant but controversial importance is the one common denominator in 
both technologies: lithium.

 

It is arguable, in retrospect, that the classic LENR of the P&F is a lithium 
reaction which is triggered by deuterium… instead of deuterium fusion. Of 
course, it could be a little of both, and thermal gain can happen with other 
electrolytes and with protium. But lithium is preferred, and the interlocking 
parameters suggest that the reaction is more complex than we have ever 
imagined, since there is little high energy radiation.

 

Plus, if and when helium is seen in the ash – it could as easily derive from 
lithium, as opposed to deuterium fission. In fact, deuterium fusion should 
produce tritium, so when that isotope is not seen, the best evidence for the 
key to the reaction shifts to lithium – instead of D+D fusion.

 

This failure to understand that LENR is primarily a lithium reaction could 
relate to 3) above which the poor reproducibility of classic LENR. 

 

The reason for this relates to weapons, National Labs, and the need to extract 
the important isotope – lithium-6 which is only 6-7% of natural lithium. 
Natural lithium is rare and expensive, and if the US Military had to pay the 
true price of enrichment of the needed lithium-6 – by writing off the entire 
inventory of Li-7, then it would have put the country at a great disadvantage 
against our enemies.

 

Therefore, and given that lithium which is depleted in lithium-6 works just 
fine for the main present use of the element - which is in advanced batteries, 
then what we see is that all of this gigantic inventory of lithium, which was 
depleted to extract Li-6 – went out on the lithium market for batteries. No one 
was the wiser, until recently.

 

Consequently, until recently, when a researcher bought the common electrolyte – 
lithium hydroxide, and did not specifically order and pay for natural isotopic 
balance – then there was little assurance that he was not getting a product 
which had already been depleted of the active isotope for LENR. 

 

The result is poor reproducibility – to the extent that the reaction is a 
lithium-6 fueled reaction. 

 

This is one explanation for the poor historic reproducibility, but there are 
others.

 

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