The ion diffusion speed in an electrolyte is only some centimeters per minute at best, while the speed in a Calutron is probably some 100 to some 1000 kilometres per second.

Therefore the mass inertia of the nucleus at this low speed has no effect. The electrolyte vessel must be some 1000 km long for this to work.

Am 03.11.2011 19:32, schrieb Axil Axil:

I don't think that as a practical matter electroplating can work to coat the particles of a micro powder but vapor disposition will work.

Furthermore, the powder can be made of bulk material, only the nanometer thick secret surface treatment needs to be heavy nickel (Ni62-64). This is not that much material at all and is a very small fraction of the total weight of nickel. Think about the colored sugar coating on the surface of an M&M but far thinner.

Using vapor disposition, isotope selection by weight can be done by using a magnetic field.

I would like to call attention to the patents of special interest that are mentioned in the Rossi 2009 patent. The ones taling about vapor disposition caught my special attention.





On Thu, Nov 3, 2011 at 8:46 AM, Berke Durak <[email protected] <mailto:[email protected]>> wrote:

    Hello everyone,

    My name is Berke and I'm not an electrochemist.  Nor a physicist for
    that matter.  (Just a comp. sci.
    guy.)  That being said, I'd like to discuss this issue nonetheless.  I
    find this subject extremely interesting.
    Also, congratulations for this well-kept and informative list.

    Some people have speculated that the heavier nickel isotopes (in
    particular Nickel-64) are the active
    elements in Rossi's alleged reaction.  I recall reading that Rossi
    claimed that the enrichment is quite
    an easy process.  Prof. S. Çelebi asked Rossi about the quantity of
    energy required to produce the
    fuel assembly, and Rossi responded that 200 W.h are enough for a 1 MW
    unit.  Since Rossi claims
    that 10 kg of (enriched) nickel is good for 180 days worth of 1 MW
    production, I suppose that this 200 W.h
    figure is what is required to process 10 kg of nickel, or maybe the
    corresponding amount of some nickel
    ore or salt.  On the other hand, there is talk of nickel powder being
    used, although I don't know if
    nanometric powder is required.

    I don't know anything about powdering, but based on some quick web
    research and back-of-the-envelope
    number crunching, it seems that 200 W.h is a reasonable amount of
    energy to pulverize 10 kg of some
    softish metal into a 70 micrometer-ish powder using commercially
    available equipment.

    Now, that doesn't solve the enrichment issue.  Note that we don't
    necessarily need pure Nickel 64.
    Some Reddit folks were talking of a 64 Ni -> 65 Cu reaction giving off
    40 keV (as gammas I suppose).
    Since 64 Ni has .00926 abundance, you'd need to enrich that isotope by
    something like 5 times.

    So how could nickel 64 be cheaply enriched x 5?  I had this weird
    idea, which may well be completely
    unfeasible.  Take a nickel electroplating bath.  There you have
    negatively charged nickel ions moving towards
    the anode.  If you place a sufficiently long bath in a magnetic field,
    won't the trajectories of the nickel ions be deviated,
    in a quantity decreasing with their mass?  If this is true, then you
    may be able to separate the heavier nickel
    ions from the lighter ones.  Note that Nickel-64 is about 10% heavier
    than the most abundant isotope, so maybe this
    won't require require too many stages, if feasible.  Basically, this
    would be a liquid-phase Calutron.  Maybe
    there is a good physical or chemical reason why this wouldn't work, so
    I'd like any knowledgeable persons
    to step forward and give their opinion.

    If this works, from the couple pages I've read on electroplating, I
    gathered that it should be possible to obtain
    relatively brittle nickel by controlling the parameters of the
    process.  This is probably a good thing,
    since after enrichment, you'll want to pulverize your nickel.

    In addition, it probably is not unreasonable to use a copper anode.
    Then, your fuel will be contaminated
    with natural copper.  So, if the fuel sample you provide for analysis
    didn't run for very long, you'll have way
    more natural copper than transmuted copper, and the isotopic
    composition may well be indistinguishable
    from that of natural copper.

    Now if that enrichment process is feasible, we need to run some
    numbers to see if 200 W.h is in the ball park
    for 5 x enrichment of Ni-64.
    --
    Berke Durak



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