Re: [Vo]:Johnson-Matthey Type A palladium

2009-09-10 Thread Jed Rothwell
One other post-script. Some people think that Fleischmann is 
misinformed about the J-M material, and it could not be their 
standard filter palladium, because that has too much silver in it to 
work well. Silver does prevent loading, but on the other hand, the 
people at BARC did report a dramatic result with the palladium 
filter. Anyway, I am not going to filter out comments by Martin Fleischmann!


- Jed



[Vo]:Johnson-Matthey Type A palladium

2009-09-09 Thread Jed Rothwell

Terry Blanton wrote:


Has there been any progress on the Matthey Pd?


As far as I know they stopped working on it after the IMRA project in 
France collapsed. The collapse was mainly caused by a fight over who 
would control the intellectual property rights to the palladium. I 
have no idea what Johnson Matthey (hereinafter J-M) learned from the 
collaboration or where the information ended up.




Are they still keeping it secret?


Probably. No idea, really.



Why would not Fleischmann want to reveal the secret assuming he knows it.


Fleischmann revealed all he knew to anyone who asked, on many 
occasions. This is a perennial subject, and attached below is my 
stock response. Briefly, what he called Type A is the palladium J-M 
developed in the 1930s for their palladium filters. As he said to me: 
Look at the data from Miles. What does it tell you? When Uncle 
Martin gives you palladium, it works. When you get the palladium from 
somewhere else, it doesn't work! Why don't people pay attention to 
that?!? He was referring to Table 10 in this document, which I have 
often referenced, and which -- as Martin says -- no one seems to pay 
any attention to:


http://lenr-canr.org/acrobat/MilesManomalousea.pdf

The material labeled JM (F/P) Pd is from Uncle Martin, and I think 
the JM Pd is the same material. Please note: anything labeled JM 
works better than other types, and the JM (F/P) Pd works 
spectacularly well. Also note that when the people at BARC tried 
using the filter palladium in situ (in a filter) it worked like 
nobody's business. As I recall the thing partly melted.


There is no mystery to why this works well, or why Fleischmann 
selected it. It works because it has structural integrity and it 
survives high loading without cracking or distorting. As you will see 
in countless references this is essential to producing the cold 
fusion effect. Fleischmann selected it because when he began this 
research he knew that it was essential that the palladium load to 
high levels, so he called up J-M and asked: What kind of palladium 
would you recommend for very high loading? And they told him. End of 
story. He is sensible guy who, as he told me, is lazy at heart and 
likes to do things the easy way. When someone knows, why not ask?


As I said, attached is a message I wrote about this in 2000, which I 
have sent to anyone who enquires about this subject.


- Jed

- - - - - - - - - - - - - - - - - - -

The Type A palladium saga

For many years Martin Fleischmann has been recommending a particular 
type of palladium made by Johnson Matthey for cold fusion 
experiments. He has been saying this to anyone who will listen, but 
very few people do. He handed out several of these ideal cathodes to 
experienced researchers, and as far as he knows in every case the 
samples produced excess heat. The material was designated Type A 
palladium by Fleischmann and Pons. It was developed decades ago for 
use in hydrogen diffusion tubes: filters that allow hydrogen to pass 
while holding back other gasses. This alloy was designed to have 
great structural integrity under high loading. It lasts for years, 
withstanding cracking and deformation that would quickly destroy 
other alloys and allow other gasses to seep through the filters. This 
robustness happens to be the quality we need for cold fusion. The 
main reason cold fusion is difficult to reproduce is because when 
bulk palladium loads with deuterium, it cracks, bends, distorts and 
it will not load above a certain level, usually ~60%, I think. Below 
85 to 90% loading bulk palladium never produces excess heat. A sample 
of palladium chosen at random from most suppliers will *never* reach 
this level of loading. You could perform thousands of tests for cold 
fusion with ordinary palladium, with perfect confidence that you will 
never see measurable excess heat. That is essentially what the NHE 
did: they performed the wrong experiment hundreds of times in 
succession, using materials which everyone knows cannot work. This is 
like trying to make a 27 story building out of doughnuts.


It seems likely to me that most of the reproducibility problems with 
bulk palladium CF would have been solved years ago if people had only 
listened to Martin Fleischmann's advice. Alas, in my experience, 
people seldom listen to advice or follow directions. Fleischmann 
sometimes compounds the problem by speaking in a cryptic, convoluted 
style and by using complex mathematical equations that few other 
people can understand. He sometimes takes a long time to respond to 
inquiries; he answered one of my questions two years after I asked. 
However, in this case he has made himself quite clear on many 
occasions. For example, he wrote:


. . . We note that whereas blank experiments are always entirely 
normal (e.g. See Figs 1 5) it is frequently impossible to find any 
measurement cycle for the Pd D2O system which shows such normal 
behaviour. Of course, in the absence of 

Re: [Vo]:Johnson-Matthey Type A palladium

2009-09-09 Thread Terry Blanton
On Wed, Sep 9, 2009 at 5:39 PM, Jed Rothwell jedrothw...@gmail.com wrote:
 Terry Blanton wrote:

 Has there been any progress on the Matthey Pd?

 As far as I know they stopped working on it after the IMRA project in France
 collapsed.

Considering Abd's goals, this gives us a lot to think about.  Ammonia
vs Argon for crystallization could very well be the key.  It's kind of
like a spacer used in the construction of the structure.  It likely
results in different containment figures for the interstitial
deuterium.

Reading the testimony before Congress in 1989 combined with this
information could be quite telling.  I think this is a geometry
problem.

Thanks, Jed.

Terry



Re: [Vo]:Johnson-Matthey Type A palladium

2009-09-09 Thread Terry Blanton
Pd is FCC at 389 pm.  Pd atom radius is 137 pm (interesting number
:-).  This leaves 115 pm which allows the 102 pm NH3 molecule ideal
for structuring but is challenging for the 188 pm Ar.

I'm gonna sleep on this.

BTW, what is the Van der Waals radius of deuterium?  (too lazy to look
it up now.)

Terry

On Wed, Sep 9, 2009 at 6:43 PM, Terry Blanton hohlr...@gmail.com wrote:
 On Wed, Sep 9, 2009 at 5:39 PM, Jed Rothwell jedrothw...@gmail.com wrote:
 Terry Blanton wrote:

 Has there been any progress on the Matthey Pd?

 As far as I know they stopped working on it after the IMRA project in France
 collapsed.

 Considering Abd's goals, this gives us a lot to think about.  Ammonia
 vs Argon for crystallization could very well be the key.  It's kind of
 like a spacer used in the construction of the structure.  It likely
 results in different containment figures for the interstitial
 deuterium.

 Reading the testimony before Congress in 1989 combined with this
 information could be quite telling.  I think this is a geometry
 problem.

 Thanks, Jed.

 Terry




Re: [Vo]:Johnson-Matthey Type A palladium

2009-09-09 Thread Terry Blanton
I would bet, if you could grow single crystal Pd ( in a NH3
atmosphere), it would load quickly.  And if you modulate it with a 26
Mhz signal (lambda = unit cell length), you could have controlled CF.

Or not.

Terry

On Wed, Sep 9, 2009 at 7:04 PM, Terry Blanton hohlr...@gmail.com wrote:
 Pd is FCC at 389 pm.  Pd atom radius is 137 pm (interesting number
 :-).  This leaves 115 pm which allows the 102 pm NH3 molecule ideal
 for structuring but is challenging for the 188 pm Ar.

 I'm gonna sleep on this.

 BTW, what is the Van der Waals radius of deuterium?  (too lazy to look
 it up now.)

 Terry

 On Wed, Sep 9, 2009 at 6:43 PM, Terry Blanton hohlr...@gmail.com wrote:
 On Wed, Sep 9, 2009 at 5:39 PM, Jed Rothwell jedrothw...@gmail.com wrote:
 Terry Blanton wrote:

 Has there been any progress on the Matthey Pd?

 As far as I know they stopped working on it after the IMRA project in France
 collapsed.

 Considering Abd's goals, this gives us a lot to think about.  Ammonia
 vs Argon for crystallization could very well be the key.  It's kind of
 like a spacer used in the construction of the structure.  It likely
 results in different containment figures for the interstitial
 deuterium.

 Reading the testimony before Congress in 1989 combined with this
 information could be quite telling.  I think this is a geometry
 problem.

 Thanks, Jed.

 Terry





Re: [Vo]:Johnson-Matthey Type A palladium

2009-09-09 Thread Jed Rothwell
Let me add a post-script. Since 2000, the ENEA researchers have put a lot of
effort into understanding and fabricating palladium. They have done a good
job. I have not made a rigorous comparison, but I think their material now
rivals the best J-M material from the IMRA program. It puts out about as
much energy per gram, and it works even more reliably and consistently. In
most tests I have heard about it is used with superwave stimulation, which
is probably contributing to the enhanced performance. It is hard to know how
much.

The ENEA samples are much smaller than the IMRA cathodes, so you have to
adjust to make the comparison.

You might say the ENEA has recapitulated whatever it was the J-M did to make
the palladium work well. Unlike J-M however, they are a national laboratory,
so their work is public. They discuss it in detail at conferences, and
publish papers. Brian Scanlan gripes that their material still constitutes a
secret sauce available only to a handful of other labs such as SRI, rather
than something available to anyone. That's true but I still think it is an
improvement over the corporate secrecy of the IMRA program.

I have no objection to corporate secrecy. A corporation must develop a thing
like this in secret. However, this is counterproductive in the early stages
of fundamental research, which is why we need national laboratories and
universities. Both have a vital role to play, but I think at this stage in
cold fusion, the open source national laboratory probably has more to
contribute.

- Jed