Steve

Hi Tut,


Did you run that hugh engine on HHO and micronic fuell alone?
No diesel or petrol, or whatever?


Steve

@ Steve.


I advice you to read my described reaction again. Notice that there are no freed electrons. You are mixing my and Edwards concept. All I do is to create nascent or atomic nitrogen - note: I do not take away electrons, that would make the process of ammonia and nitrous oxide formation impossible. All I do is to create a situation where available space within the atomic nitrogen can be re established using available electrons in the hydrogen atom.


The reactor Alessandro is promoting was developed together with Michael Nunerlay and was a terminated collaboration in the same style that me and Alessandro had.

Thank you Iontruster for pointing that out to me. I apologise for not reading proper your post.
Let me ask you the same question as i did towards Alesandro.
Have you build such reactor that re-establishe the atoms with all available electrons?
I find it very fascinating!

Steve

Thanks for the pdf.

I also had contact with Edward and with Tutanka.
There have been many discussions on how to create a possible new mix of gasses.
For sure, if you can ionize nitrogen and remove the freed electrons!, then maybe the ionized atom will attack the hydrogens electron.

I have achieved myself a better burnrate of H and O with help of ionized ambient air. Meaning Nitrogen and oxygen.
My engine much better, like 25% more power then on HHO and normal ambient air.
So, yes. Thats a good direction to research into.

Tutanka seems to have build plans ready, but he is asking 200 euro's for them, which is a lot of money for a normal Joe.
But is his reactor really works, then its worth every penny.

About getting water in your oil of engines.
That might happen. I havent seen it in my tests, but those engines never ran longer then 1 hour orso.
For sure, a normal ICE is not build for water.....


Steve

Start here your topics on the water injector with ambient airgasprocessor system.

Steve

Thanks Bubz   

I already made such an ion wind gun....

http://www.ionizationx.com/index.php/topic,1265.msg15000.html#msg15000


Steve

Manual with schematics

Another patent

Possible kits

http://www.imagesco.com/kits/negative-ion-generator.html

My setup will be like this one..




Steve

Hi,

Here is a patent about creating ion wind.
That is a way to ionize the ambient air.
My first test will be with a similair device.

Steve

Ambient  airgasprocessor setup.

Thanks for sharing Jim 

Hi dandaman,

It seems you dropped an empty post here....
What did you wanna post?

Steve

Hydrogen Gas Gun


In order to obtain gas atoms in a critical state, a device called the Hydrogen Gas Gun (HGG) is used and it’s mounted on top of the Resonant Cavity Assembly. This circuit strips and captured free electrons from the gas atoms, tuning them into a highly combustible gas ions. The resistive elements; R4, R6 and R7, the dielectric constant of the gas (Rg) as well as the isolated ground (W) make sure electron flow or deflection won’t take place, keeping the gas in a permanent critical state during its process.
The dislodged electrons are consumed by a passive electric element that would convert its energy into heat or light or even both, such as a light bulb. Or it can be repelled by a gas ion created by laser.

Thermal Explosive Energy

When exposing the combustible gas ions from the Gas Resonant Cavity to a thermal spark of a heat zone, it ignites, releasing what’s called a Thermal Explosive Energy which is beyond the Gas-flame level.

This thermal atomic interaction is caused when the burning of ionized gases – in this case from water – doesn’t reunite the hydrogen and oxygen ions creating water again. The reason is that the HGG caused the oxygen atom to lose more electrons, preventing it from reaching the stable state. The laser energy from Va, Vb and Vc also weakens the bonds between the nucleus and its orbiting electrons. As the attraction forces are getting stronger between the atoms due to the absence of some covalent electrons, the oxygen ions latches onto the hydrogen electrons. This atomic thermal reaction would be known now as Hydrogen Fracturing Process which can be easily controlled by changing the amplitude of the input voltage.

Most of Stans video's contain info about a spherical resonant cavity.
How could we build a spherical 304 SS cavity?

Steve

Ha, you used the famous crowbar (Ravi / Hydrocars) diode technique.
 
Nice schematic!

How has everyone been? I saw Dankie over on the other forums and I thought I'd check in and see what was cooking. Been working on solid state systems over the past year or two. Found some interesting things with high voltage driving coils. Anyone duplicated the JLN tests? They looked pretty simple and promising.

Tad

Hi Tad,
 
No, nobody did a succesfull replication of JNL. Neither we could replicate your succes as well.
Have you ever found the details of your succesful tests of the resonance setup?
 
Give Dankie our regards, btw...
 
Steve

Quote from: Steve on September 14, 2010, 13:17:20 pm

I have not yet had the opportunity to duplicate this portion of the experiment but, in time I vill. 

I'll wait for that

 

In. the original setup that Stan Meyer showed us, he used 36 volts as the basic potential applied to the reaction chamber. He also commented that stainless steel ( 410 not 403 ) was the only metal that could be used as oxides formed with all others. His original chamber used 18 inch long by 0.375 inch diameter (o.d.) rod surrounded by 1 inch diameter (i.d.) 16 inch long pipe. The reason for the difference in length is for mechanical ease of construction. My prototype used 14 inch long rod and 12 inch long pipe of similar diameters as the drawing indicates.   Having a severe lack of parts diversity here in Sri-Lanka, I was only able to obtain a 24 volt. 8 amp transformer and built my circuitry around that. The final output is 20 volts with Ml reading 10 amps to the pulsing circuit which generates a symetricel squarewave ( 50% duty cycle ) to the flyback inductor connected in series with the chamber as the schematic shows. The flyback high voltage spike is directed across the chamber via c* end d*. The use of a high voltage spike alone, without the current being delivered through the liquid, will not cause the disassociation to take place. This I verified using an ignition coil in place of the inductor and applied the secondary with halfwave rectification and blocking capacitor to prevent burn out to the chamber with no results. Apparently the current in the water aligns the molecules approprately to allow the high voltege spike to do its workr which in my opinion is the stimulation of molecular resonance. Once Stan's unit was made to begin breakdown (which takes 6 to 8 seconds) he was able to reduce both current and voltage to miniscule proportions. I attribute this to sympathetic oscillation of the aligned molecules, requiring very little in the way of additional excitation. A phenomena akin to Tesla `s super resonance... resulting in Stan discovering that he only had to supply three pulses in ten to satisfy the requirement of the chamber. I have not yet had the opportunity to duplicate this portion of the experiment but, in time I vill.   Duplication of the device described in these pages, however, will produce the phenomena and hopefully launch other enterprising end inventive souls on to designing their own refined models. It would be nice to have feedback so that we can all collectively work to bring about the transition to non-pollution energy.   P.S.- Tho electrical circuit is by no means optinised, but represents instead the result of parts availability here. Any good technician could improve on it quite readily.   There are two primary frequencies that produce the best results. They are. 14372 Hz and 43430 Hz. The former is about 50% more efficient, but it seems that just about any frequency between 9 KHz and 143762 KHz works quite well. 1) This is because the nature of the wave form ( a spike ) is rich in harmonics and one of them is bound to be close to one of the two primary frequencies.   Use of permanent magnets may also increase efficiency. I'll give you the outcome of that attempt in my next letter along with the plans for what I hope to be a much improved version.   Note: Sub-harmonics of the two primary frequencies at which dissociation will occur:
43430 Hz             143762 HZ  SUBHARMONIC          SUBHABMONIC  1st 21715    HZ      1st 71881    HZ  2nd 14476.67 HZ      2nd 47920.67 HZ  3rd 15517.5  HZ      3rd 35840.1  HZ  4th 8686     Hz      4th 28752.4  HZ    *1500 VOLTS IS THE MINIMUM REQUIRED FOR MOLECULAR RINGING TO BEGIN.   The ball is now in your court.   Let's get the game started and have as many players as possible.   From the legal stand point it can be argued in an international court of law that the vital need of this technology by every nation to aleviate the critical threat to our environment globally is so greet as to justify nullification of proprietry rights if those rights are used to delay or prevent distribution of the technology and if such delay or prevention - including measured and / or levied distribution so as to restrict or limit its use, or for the purposes of financial profit isolate significent economic groups from its use and if such acts previously mentioned can be shown to cause an increased danger to life, persons involved in such acts can be convicted of intent to do bodily harm by crime of omission.   (ANY MATERIAL SENT TO `TUNING IN' WILL BE FORWARDED TO THE ABOVE WRITER.)   Back to the Mad Scientist's Lair   
 
 
    Source publication: Unknown
Scanned from very bad photocopy.   
 
 

Ok, new life into this subject.
Have you ever noticed that Meyer used 2 different type of descriptions for the diode in the VIC schematics?
Have a look at the two drawings attached.

As Hardkrome pointed out, my 2 cents are that the switching diode must been seen as a SCR diode.....

Steve