Re: Gold nano particles = resonant hydrino catalyst?

[Frederick Sparber]

They still use that ruby-red"Colloidal Gold Sol" .  :-)

 

http://www.devicelink.com/ivdt/archive/01/03/001.html

 

"As early as the first decade of the twentieth century, colloidal gold sols containing particles smaller than 10 nm were being produced by chemical methods.¹ However, these inorganic suspensions were not applied to protein labeling until 1971, when Faulk and Taylor invented the immunogold staining procedure.² Since that time, the labeling of targeting molecules, especially proteins, with gold nanoparticles has revolutionized the visualization of cellular and tissue components by electron microscopy."

 

----- Original Message -----

From: Frederick Sparber

To: vortex-l

Sent: 4/2/2006 7:40:04 PM

Subject: Re: Gold nano particles = resonant hydrino catalyst?

Hi Robin.

 

This in line with the free energy release of the spontaneously formed  Double Layer at the

Colloidal Gold-H2O interface. I used Colloidal Gold obtained from a medical supply  house

(it is/was used in spinal injection) in water heat pipe research in the late 1960s.

>

> Though the ice did not melt when heated by low-intensity laser alone, it
> dissolved once a gold nanoparticle was embedded, said the scientists, whose
> findings have been published online by the journal Nano Letters
>

The laser photons should release the 1/2 CV^2 energy stored from

the free energy Double Layer. So does the electrolysis of water and many

other OU effects associated with agitation of the H2O-Solid interface.

 

Fred

 

http://electrochem.cwru.edu/ed/encycl/art-c03-elchem-cap.htm

 

"The Helmholtz region capacitance "C_H" is of special significance for electrochemical capacitors since it is directly dependent on accessible electrode area and has large values (relative to those for regular dielectric capacitors) between about 16 µF/cm² and about 40-50 µF/cm², depending on electrode potential, the chemical nature of the metal surface, chemical nature of the solvent, and the types of ions (and their solvation by the solvent) present in the electrolyte solution."

 

"Hence, it is seen that with large specific-area porous electrodes, for example at carbons having say 1000 m²/g of material and exhibiting, say, 15 µF/(real cm²) of double-layer capacitance in some suitable electrolyte solution, the accessible capacitance "C" is 1000 (m²/g) × 10,000 (cm²/m²) × 15 (µF/cm²) = 150 million µF/g, that is 150 farads/g, a very large capacitance! Hence the term "supercapacitors" or "ultracapacitors" for devices based on double-layer capacitance at high-area substrates."