A new conditioning idea

[Farlander]

Hey guys...
I was conditioning my plates with 12v 1amp.  I was told that short duration of low amps was best at first.

I was also told that drying the cell in between sessions would aid the buildup of said oxide layer...

So I took the plates out and set them vertically to dry.  Then I had the idea... why not turn on the juice and boil off the remaining water?  Eventually, no current will flow.  Does this work?  I'll let you know how it goes...


Also, is there any reason to expect that + - + - + - cell configuration will yield more gas than just one + - given the same input power?

[kinesisfilms]

conditioning is a lie.

[sucahyo]

I think conditioning meant for bob boyce replication will not work for normal electrolysis or for stanley meyer replication. Stanley meyer replication conditioning will not work for normal elctrolysis.  But they all share the same preconditioning in order to make the plate less magnetic or even, either with exposing to inert gas argon, applying even heat, etc.

[Hydro-Cell]

conditioning your plates is useful, in the way that firstly you rid the plates of excess iron content which prevents the water from discolouring and stopping hho production. the oxide layer is supposed to yeild more hho due to the way the surfaces become rough thus containing more surface area.

[CrazyEwok]

No one has answered the questions asked yet. Since no-one has answered you i would say that no-one has tested it. if you want you can try different ways to condition your plates personally if it takes me 3 months of conditioning to get a cell that produces no brown much then i will be very happy with that invested time... i suggest trying your dry voltage application to increase the dry time but be careful i would hate for you to create a spark and ignite any wofting H...
as for your question on the +-+-+- configuration i have often thought this myself along with how they are connected... squence vs parallel... maybe you can tell us???

I have also wanted to know with the the guys that creat the tube based reaction chambers if they have thought about putting some holes in the electrodes to allow water to flow into the gaps once it has been electrolized... they have these long tubes with a very small gap at the top that as far as i can tell is meant to allow water to flow the full length of the tube and allow the gases escape... and design for them maybe to flow the water into the gap of the tubes and have the other end as the gas exit point... thus shrinking the thickness of their cells... All theory use as you will.

I will be very interested in seeing the effientcy of your cell if you use a +-+-+-+- configuration. Also please let us know if parallel or squence works better?