Jones, Good insights!  Assuming temp control to keep the magnetite / hematite 
populations roughly in balance what other parameters could we vary to force the 
populations to oscillate? Electrical, magnetic, microwave, gas pressure, etc. 
etc. It seems like a low cost effect to investigate with a potential windfall 
of valuable data even if it doesn't turn out to be "THE" missing piece of the 
puzzle [and if it is the missing piece you just saved the world!]
Fran


From: Jones Beene [mailto:[email protected]]
Sent: Sunday, January 17, 2016 6:09 PM
To: [email protected]
Subject: EXTERNAL: [Vo]:Iron oxide, hydrogen and a mechanism for densification


Here are some factoids to toss around in pursuit of UDD on an industrial scale. 
This does not seem to be what Holmlid is doing, but it makes sense anyway, at 
least on paper.

Magnetite is iron-oxide with the chemical formula is Fe3O4 ratio 1:1.33 (iron 
to oxygen atoms)

Hematite is iron-oxide with the chemical formula is Fe2O3 ratio 1:1.5 (iron to 
oxygen)

There are striking differences in the physical properties of the two oxides - 
especially electrical conductivity and magnetic susceptibility. Oxygen can be 
strongly paramagnetic and can cause superparamagnetism at the nanoscale. Thus 
varying oxygen content of the oxide is the key.

When hematite is combined with hydrogen and heat, some of the oxide will be 
reduced to magnetite and steam, but then then magnetite will be combined with 
steam and heat and be oxidized back to hematite.  This can happen rapidly, on a 
time scale of picoseconds. Thus, a shifting balance between the two oxides is 
reached at equilibrium, when hematite is stored in the presence of pressurized 
deuterium and heat. The secondary results of this see-saw - nanomagnetism - 
should lead to hydrogen densification due to magnetic interactions.

The two oxides have different, but similar, physical structure, based on 
hexagonal nanoporosity and will hold varying amounts of hydrogen. But rapid 
changes in magnetization would be the avenue leading to UDD.

This process may sound similar to the deuterium uptake in palladium, seen in 
cold fusion... but in contrast the pores in iron-oxide are an order of 
magnitude larger and are in the range of the Casimir force, whereas the 
palladium matrix is too tight to benefit from Casimir dynamics.

Specific gravity of iron: 7.84  g/cm3; Specific gravity of oxygen: 1.1 g/cm3.

Density of Magnetite: 5.175 g/cm3 (Measured); 5.20 g/cm3 (Calculated specific 
gravity).

Density of Hematite: 5.15 g/cm3 (Measured); 5.30 gm/cm3 (Calculated specific 
gravity).

Thus we can see that in comparing the two oxides, hematite "should be" less 
dense (than it is in actuality) based on its higher oxygen content and the 
lower specific gravity of oxygen. This means that magnetite has slightly 
greater nanoporosity but both are significantly nanoporous. It is the change in 
porosity, when going from H-to-M-to-H rapidly - which is important.

When hydrogen enters the picture, as a gas - it is stored in the nanopores and 
becomes reactive, based on temperature - but as the oxides change from H 
(hematite) to M (magnetite) and back again, trillions of times per second, the 
net effect is like a pump, or a piston engine. Rapid change is pressurization 
and magnetization could set the stage for gradual densification over time. 
Temperature control would be important.

Based on these parameters, it should be possible to make significant amounts of 
UDD over an extended time period, simply by storing pressurized deuterium in 
iron-oxide - at temperature near the Néel temperature of ~950 K (675 C) ... for 
weeks to months. Something similar may happen with nickel-oxides at lower 
temps, but being less reactive, not as robust. The chances of success with this 
kind of static densification technique would seem be far greater with 
iron-oxides than nickel oxides.

Jones

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