Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2015-01-19 Thread mixent
In reply to  Jones Beene's message of Mon, 29 Dec 2014 10:06:31 -0800:
Hi,
[snip]
First, we can note that after the hydrogen is released from LiAlH4, the
lithium remains alloyed to aluminum, since there is no intrinsic mechanism
to separate the metals below the Li boiling point of 1342 °C which is
closely approached, and this is notably where maximum COP occurs for
Parkhomov.  In an alloy, lithium atoms near the boiling point would react
differently than as an element. “Near-phase-change” could be the key to the
exotherm and to promoting double ionization of Li.

According to wiki (http://en.wikipedia.org/wiki/Lithium_hydride) a less common
method of the preparation of LiH is by heating LiAlH4 (200 ºC).

Furthermore: Thus removal of H2 requires high temperatures, well above the 700
°C used for its synthesis.

...so it would seem that at 1300 ºC it ought to decompose readily enough.

Regards,

Robin van Spaandonk

http://rvanspaa.freehostia.com/project.html



Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2015-01-19 Thread mixent
In reply to  Jones Beene's message of Mon, 29 Dec 2014 10:06:31 -0800:
Hi,
[snip]
To back up a bit – as far back as the early nineties, lithium was claimed to
be responsible for most of the energy gain in electrolytic reactions, since
as an doubly positive ion, Li has the characteristic energy “hole” define by
Mills for promoting ground state redundancy. The first IP is 5.4 eV and the
second is 75.64 eV and together, they present a deficit which is very close
to the value of (3 x 27.2 = 81.6 eV). Nickel provides two more “holes” so
the net reaction being demonstrated both here and for 25 years does fit into
Mills’ model superficially. Yet achieving the ~76 eV to create the “hole” is
almost out of the question for electrolysis in terms of probability and even
at 1300 degrees it would be rare. Yet this can happen readily during
energetic phase change (as Parkhomov has apparently demonstrated).


This is a misunderstanding. Li *metal atoms* present a hole (or energy sink) by
having two electrons for which the sum of the binding energies is 81.6 eV.

I.e. H + Li (note metal atom, not ion!) = Hy[n=1/4] + Li++ + excess energy.

IOW, by donating 81.6 eV to a Lithium atom(!), the H atom shrinks to H[n=1/4]
while at the same time the Li atom uses the energy released by the H atom to
become ionized to Li++.

In short the shrinkage reaction neither needs nor wants Li++. Rather it produces
it as an end product through the shrinkage reaction. The input material is an H
atom and a Lithium atom, both of which are readily available upon thermal
decomposition of LiH.

Once the catalytic reaction is complete, the newly formed Li++ ion may then, at
it's own discretion, reacquire a pair of electrons from the environment,
becoming neutralized in the process, after which it is once again available to
act as a catalyst for another shrinkage reaction.

Note also, that in electrolysis experiments both H and Li atoms will form at the
cathode, though the Li atom will be short lived, as it will rapidly react with
water. This means that the chances of living long enough to catalyze a shrinkage
reaction with a Hydrogen atom are small in electrolysis reactions.
Regards,

Robin van Spaandonk

http://rvanspaa.freehostia.com/project.html



Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2015-01-19 Thread Bob Cook
The boiling point for Li in side a nano particle may occur at a different 
temperature than 1342 C.  The local electric and magnetic conditions may 
make a big difference in how tight the Li is bound to the Al.


Bob
- Original Message - 
From: mix...@bigpond.com

To: vortex-l@eskimo.com
Sent: Monday, January 19, 2015 7:54 PM
Subject: Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and 
lithium aluminum hydride



In reply to  Jones Beene's message of Mon, 29 Dec 2014 10:06:31 -0800:
Hi,
[snip]

First, we can note that after the hydrogen is released from LiAlH4, the
lithium remains alloyed to aluminum, since there is no intrinsic mechanism
to separate the metals below the Li boiling point of 1342 °C which is
closely approached, and this is notably where maximum COP occurs for
Parkhomov.  In an alloy, lithium atoms near the boiling point would react
differently than as an element. Near-phase-change could be the key to the
exotherm and to promoting double ionization of Li.


According to wiki (http://en.wikipedia.org/wiki/Lithium_hydride) a less 
common

method of the preparation of LiH is by heating LiAlH4 (200 ºC).

Furthermore: Thus removal of H2 requires high temperatures, well above the 
700

°C used for its synthesis.

...so it would seem that at 1300 ºC it ought to decompose readily enough.

Regards,

Robin van Spaandonk

http://rvanspaa.freehostia.com/project.html




Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2015-01-19 Thread Bob Cook

You noted:

Once the catalytic reaction is complete, the newly formed Li++ ion may 
then, at

it's own discretion, reacquire a pair of electrons from the environment,
becoming neutralized in the process, after which it is once again available 
to

act as a catalyst for another shrinkage reaction.

I would add that the neutral Li would also act as a good heat transfer 
agent, if it did not react, keeping the structure from getting to hot and 
changing shape.


Bob

- Original Message - 
From: mix...@bigpond.com

To: vortex-l@eskimo.com
Sent: Monday, January 19, 2015 8:12 PM
Subject: Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and 
lithium aluminum hydride



In reply to  Jones Beene's message of Mon, 29 Dec 2014 10:06:31 -0800:
Hi,
[snip]
To back up a bit - as far back as the early nineties, lithium was claimed 
to

be responsible for most of the energy gain in electrolytic reactions, since
as an doubly positive ion, Li has the characteristic energy hole define 
by

Mills for promoting ground state redundancy. The first IP is 5.4 eV and the
second is 75.64 eV and together, they present a deficit which is very close
to the value of (3 x 27.2 = 81.6 eV). Nickel provides two more holes so
the net reaction being demonstrated both here and for 25 years does fit 
into
Mills' model superficially. Yet achieving the ~76 eV to create the hole 
is
almost out of the question for electrolysis in terms of probability and 
even

at 1300 degrees it would be rare. Yet this can happen readily during
energetic phase change (as Parkhomov has apparently demonstrated).



This is a misunderstanding. Li *metal atoms* present a hole (or energy sink) 
by

having two electrons for which the sum of the binding energies is 81.6 eV.

I.e. H + Li (note metal atom, not ion!) = Hy[n=1/4] + Li++ + excess energy.

IOW, by donating 81.6 eV to a Lithium atom(!), the H atom shrinks to 
H[n=1/4]

while at the same time the Li atom uses the energy released by the H atom to
become ionized to Li++.

In short the shrinkage reaction neither needs nor wants Li++. Rather it 
produces
it as an end product through the shrinkage reaction. The input material is 
an H

atom and a Lithium atom, both of which are readily available upon thermal
decomposition of LiH.

Once the catalytic reaction is complete, the newly formed Li++ ion may then, 
at

it's own discretion, reacquire a pair of electrons from the environment,
becoming neutralized in the process, after which it is once again available 
to

act as a catalyst for another shrinkage reaction.

Note also, that in electrolysis experiments both H and Li atoms will form at 
the
cathode, though the Li atom will be short lived, as it will rapidly react 
with
water. This means that the chances of living long enough to catalyze a 
shrinkage

reaction with a Hydrogen atom are small in electrolysis reactions.
Regards,

Robin van Spaandonk

http://rvanspaa.freehostia.com/project.html




[Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2014-12-29 Thread Orionworks - Steven Vincent Johnson
Mills recently had more uncomplimentary things to say about recent LENR
research. See SCP thread:

 

a mixture of nickel and lithium aluminum hydride

 

See thread:

 

https://groups.yahoo.com/neo/groups/SocietyforClassicalPhysics/conversations
/topics/4274

 

 


*

 

A poster, James Bowery, brought up a discussion about Alexander Parkhomov's
recent work. James posted:

 

 Alexander Parkhomov, a Russian scientist:

 http://www.researchgate.net/profile/A_Parkhomov

 

 claims he has replicated Rossi's E-Cat using a mixture of nickel and

 lithium aluminum hydride.

 

 He provides an English translation of his report:

 

 http://www.e-catworld.com/wp-content/uploads/2014/12/Lugano-Confirmed.pdf

 

 In his replication, he measures heat output by completely boiling off a
fixed amount of

 water rather than inferring power output via infrared camera.  He reports
no radioactivity or energetic gammas. 

 

Randy's initial reply:

 

 How does he know what is in the Ecat cell?  LiAlH4 + Ni as a hydrogen 

 dissociator run at elevated temperature is disclosed in my patents.  

 They are filed in Russia.

 

James Replied:

 

 A few people have been speculating for some time that Rossi's E-Cat

 nickle-based catalytic system was actually a takeoff of 

 Hydrocatalysis Power Corp's nickle-based catalytic technology.

 

 One might further speculate that Dr. Parkhomov took that seriously enough

 to look into the BLP Russian patent filings involving LiAlH4 + Ni.

 

Randy's follow-up reply:

 

 In general, I have found the rogues left in that bogus cold fusion field
are

 very poor at science, self deluded, or dishonest.  Telling is that I was

 flamed when I published on a catalytic reaction involving light hydrogen

 and nickel, and now it is the main event.  Of course, no one admits to my

 work.  Shameful.  Good luck to them getting light hydrogen to fuse or
undergo

 a nuclear reaction.

 

 None the less I think that it is a mistake to use a hydrogen porous vessel

 for a hydrino reaction.

 


*

 

Obviously there is no love lost between Dr. Mills and the loosely associated
LENR community - at least it would seem from Dr. Mills' POV. Of particular
interest to me, Dr. Mills states (and also complains that) he had once been
flamed when he published work on ... a catalytic reaction involving light
hydrogen and nickel, and now it is the main [LENR] event. Mills initially
seems to be saying that he finds many LENR researchers to be, in his
opinion,  very poor at science, self deluded, or dishonest. But then he
follows up with the comment that he had been flamed and that no on admits
to [his prior] work. IMO, that would seem to contradict Mills' prior claim
that he finds LENR research to be a bogus science filled with some dishonest
researchers. I tend to think Mills makes such statements primarily for
strategic BLP business reasons rather than wanting to make an honest effort
to discuss any underlying scientific content of the latest LENR data. From
Mils' POV, they are unwelcomed distractions.

 

IOW, Move along, move along... nothing to see here. 

 

I would add, it's an understandable position any CEO might take for
strategic BLP business reasons - primarily to maintain control over their
RD plans. But from the perspective of pursuing scientific inquiry...it
stinks.

 

Comments?

 

Regards,

Steven Vincent Johnson

svjart.orionworks.com

zazzle.com/orionworks



Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2014-12-29 Thread James Bowery
Quite aside from the business consequences of his comments, my perception
of Mills is that the failure of the LENR community to take his theory more
seriously -- particularly given the LENR community's theoretic poverty --
is bad science, independent of the quality of the empirical work of the
LENR community.

If his theory is as coherent, all encompassing and supported by experiment
as he believes it is, then his contempt for the LENR community's ignorance
of it -- particularly given the dominant culture's hostility to it -- is
quite understandable.

On Mon, Dec 29, 2014 at 10:34 AM, Orionworks - Steven Vincent Johnson 
orionwo...@charter.net wrote:

  Mills recently had more uncomplimentary things to say about recent LENR
 research. See SCP thread:



 a mixture of nickel and lithium aluminum hydride



 See thread:




 https://groups.yahoo.com/neo/groups/SocietyforClassicalPhysics/conversations/topics/4274






 *



 A poster, James Bowery, brought up a discussion about Alexander
 Parkhomov's recent work. James posted:



  Alexander Parkhomov, a Russian scientist:

  http://www.researchgate.net/profile/A_Parkhomov

 

  claims he has replicated Rossi's E-Cat using a mixture of nickel and

  lithium aluminum hydride.

 

  He provides an English translation of his report:

 

 
 http://www.e-catworld.com/wp-content/uploads/2014/12/Lugano-Confirmed.pdf

 

  In his replication, he measures heat output by completely boiling off a
 fixed amount of

  water rather than inferring power output via infrared camera.  He
 reports no radioactivity or energetic gammas.



 Randy's initial reply:



  How does he know what is in the Ecat cell?  LiAlH4 + Ni as a hydrogen

  dissociator run at elevated temperature is disclosed in my patents.

  They are filed in Russia.



 James Replied:



  A few people have been speculating for some time that Rossi's E-Cat

  nickle-based catalytic system was actually a takeoff of

  Hydrocatalysis Power Corp's nickle-based catalytic technology.

 

  One might further speculate that Dr. Parkhomov took that seriously enough

  to look into the BLP Russian patent filings involving LiAlH4 + Ni.



 Randy's follow-up reply:



  In general, I have found the rogues left in that bogus cold fusion field
 are

  very poor at science, self deluded, or dishonest.  Telling is that I was

  flamed when I published on a catalytic reaction involving light hydrogen

  and nickel, and now it is the main event.  Of course, no one admits to my

  work.  Shameful.  Good luck to them getting light hydrogen to fuse or
 undergo

  a nuclear reaction.

 

  None the less I think that it is a mistake to use a hydrogen porous
 vessel

  for a hydrino reaction.




 *



 Obviously there is no love lost between Dr. Mills and the loosely
 associated LENR community - at least it would seem from Dr. Mills' POV. Of
 particular interest to me, Dr. Mills states (and also complains that) he
 had once been flamed when he published work on ... a catalytic reaction
 involving light hydrogen and nickel, and now it is the main [LENR] event.
 Mills initially seems to be saying that he finds many LENR researchers to
 be, in his opinion,  very poor at science, self deluded, or dishonest.
 But then he follows up with the comment that he had been flamed and that
 no on admits to [his prior] work. IMO, that would seem to contradict
 Mills' prior claim that he finds LENR research to be a bogus science filled
 with some dishonest researchers. I tend to think Mills makes such
 statements primarily for strategic BLP business reasons rather than wanting
 to make an honest effort to discuss any underlying scientific content of
 the latest LENR data. From Mils' POV, they are unwelcomed distractions.



 IOW, Move along, move along... nothing to see here.



 I would add, it's an understandable position any CEO might take for
 strategic BLP business reasons - primarily to maintain control over their
 RD plans. But from the perspective of pursuing scientific inquiry...it
 stinks.



 Comments?



 Regards,

 Steven Vincent Johnson

 svjart.orionworks.com

 zazzle.com/orionworks



RE: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2014-12-29 Thread Jones Beene
From: Orionworks - Steven Vincent Johnson 

 

Mills recently had more uncomplimentary things to say about recent LENR
research. See SCP thread: a mixture of nickel and lithium aluminum hydride
See thread:

 

https://groups.yahoo.com/neo/groups/SocietyforClassicalPhysics/conversations
/topics/4274

 


*

 

Mills is probably correct about his large contribution to the field - but
sadly misinformed about the limits of his patent coverage. He apparently
still believes that he can patent a theory. His patents do not anticipate
the high temperature ceramic reactor, nor do they anticipate SPP, nor the
key feature of near-phase-change in Li-Al alloy. Yes - he deserve more
credit for his insight than he gets, but he should acknowledge that his
actual devices have been one failure after another – going back 20 years. 

 

This inability to take a useful theory from Lab to market is hard to fathom
– but the reality of having nothing to demonstrate, which can be
independently verified - is one reason why Mills is routinely ignored by
peers… well … he is arrogant enough to think he has no peers, but that is
part of the problem, isn’t it? 

 

The interest in lithium  as either reactant or catalyst has been jolted by
the Parkhomov report, which if anything appears to be much more convincing
than the Levi report on which it was based. Not to mention – far more
convincing than the madly sparking seam welder, LOL. Yet… the Russian
results do look closer to the f/H (fractional hydrogen) reaction than
anything nuclear.

 

OTOH, this reaction is not what BLP wishes that they had covered in IP.
Close, but mention of one catalyst is not close enough when half the
periodic table qualitied under your theory. The probative question is - how
does aluminum facilitate access to the deep Rydberg ionization potential of
lithium, in a way which has been missed by everyone including Mills? 

 

First, we can note that after the hydrogen is released from LiAlH4, the
lithium remains alloyed to aluminum, since there is no intrinsic mechanism
to separate the metals below the Li boiling point of 1342 °C which is
closely approached, and this is notably where maximum COP occurs for
Parkhomov.  In an alloy, lithium atoms near the boiling point would react
differently than as an element. “Near-phase-change” could be the key to the
exotherm and to promoting double ionization of Li.

 

To back up a bit – as far back as the early nineties, lithium was claimed to
be responsible for most of the energy gain in electrolytic reactions, since
as an doubly positive ion, Li has the characteristic energy “hole” define by
Mills for promoting ground state redundancy. The first IP is 5.4 eV and the
second is 75.64 eV and together, they present a deficit which is very close
to the value of (3 x 27.2 = 81.6 eV). Nickel provides two more “holes” so
the net reaction being demonstrated both here and for 25 years does fit into
Mills’ model superficially. Yet achieving the ~76 eV to create the “hole” is
almost out of the question for electrolysis in terms of probability and even
at 1300 degrees it would be rare. Yet this can happen readily during
energetic phase change (as Parkhomov has apparently demonstrated).

 

Going beyond Mills - the interatomic spacing for Al-Li alloy is unique at
3.2 Angstrom which is far closer than the crystal spacing in either pure
lithium or aluminum or any other alloy of the two, indicating a high order
of structure – but only in the 1:1 alloy. Therefore the phase change for
“boil-off” of lithium would be expected to be extraordinarily energetic – in
the sense of recalescence and promoting double ionization. Recalescence is a
temporary increase in power, sometimes extreme, which occurs when molten
metal goes through phase-change on cooling. The “near boil-off” of the
double positive ion would expose Li++ to hydrogen gas, even without complete
boil-off. Plus, the phase change can be strongly exothermic even without
ground state redundancy; but… not net gainful, since it should be reversible
without an intrinsic power source … which Mills’ theory describes. 

 

Three cheers for the redundant ground state part of the theory - which he
got right! 

 

So yes, Mills theory can explain the major part of the Parkhomov experiment,
but not all of it. And no, this device is not protected by any BLP patent
which I have seen. The theory of operation is not patentable in itself, only
a device - so even though Mills could (and possibly should) win a “big
prize” one day  - for the basic theory - he may miss the economic bounty of
a working device.

 

Unless that wildly sparking seam-welder does work for more than a few hours
at a time… J

 



Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2014-12-29 Thread Jed Rothwell
Sigh . . . I had forgotten what a jerk Mills can be.

He owes everything to Fleischmann  Pons -- as do we all. If they had not
published, he never would have thought to do his first experiments.

- Jed


Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2014-12-29 Thread James Bowery
Its not clear that he owes everything to Fleischmann  Pons.  If they had
not published, he might well have developed his theory from his original
motivation, which was high temperature superconductivity.  Given fractional
Rydberg states its clear that their pusuit would be a new source of
energy.  While it is certainly no fault of Fleischmann  Pons, it may even
be the case that Mills would have marketed an energy technology years
earlier if they had not published and triggered hysterical opposition from
the authorities.

Stolper's book on Mills
http://www.amazon.com/Genius-Inventor-controversy-historical-contemporary/dp/1419643045
has passages such as that concerning high-temperature superconductivity on
p105:

Mills began the sustained work on his reformulation of quantum theory in
the fall of 1988, when he became interested in high-temperature
superconductivity.  He wondered whether it would be possible at room
temperature.


He soon found that he couldn't get a grip on the problem with standard
quantum mechanics... In Anderson's opinion, superconductivity needed an
entirely new theory.  Mils carried that opinion to its logical extreme,
which was further than any other investigator of superconductivity cared to
go:  develop a new quantum theory, not just a new theory of
superconductivity



On Mon, Dec 29, 2014 at 12:07 PM, Jed Rothwell jedrothw...@gmail.com
wrote:

 Sigh . . . I had forgotten what a jerk Mills can be.

 He owes everything to Fleischmann  Pons -- as do we all. If they had not
 published, he never would have thought to do his first experiments.

 - Jed




Re: [Vo]:Mills critical critiques on LENR: a mixture of nickel and lithium aluminum hydride

2014-12-29 Thread Jed Rothwell
James Bowery jabow...@gmail.com wrote:

Its not clear that he owes everything to Fleischmann  Pons.


His first experiments were electrochemical with nickel, similar to FP's
experiments with Pd. As I recall, he said he was prompted to do them by the
reports of cold fusion.

He also repeatedly claimed that he can explain cold fusion based on his
theory. Now he says cold fusion is bogus and the researchers are very
poor at science, self deluded, or dishonest. You do not need his theory to
explain bogus results, do you? You don't need any theory. You just
dismiss them. You toss them out, along with the laws of thermodynamics and
calorimetry going back to Lavoisier. All wrong. Hundreds of world class
experts from hundreds of major laboratories are all very poor at science.
Who knew that National Labs and places like BARC were staffed by such
dunderheads?

Even if his theories prove right, personally he is yet another tiresome,
arrogant fool.

- Jed