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Author: Subject: Advice on scaled-up H20 Electrolysis?
slightlymadscience
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[*] posted on 1-4-2008 at 10:40
Advice on scaled-up H20 Electrolysis?


I've done small-scale H20 and NaOH electrolysis with test tube/beaker (crucible with NaOH) set ups using DC batteries and carbon electrodes. My question comes up after scaling up considerably.

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I built a plexiglass tank (holds at least 5 gallons) that has gas traps on either side (with valves), and the electrodes are an array of 11 stainless steel plates (switch plate covers) on either side. The electrodes are separated by a distance of over 30 cm. The power supply is an old solid-state car battery charger (12 volts, settings of 2/5/10 amps). I've used tap water, and distilled water, and have tried NaCl and NaHCO3 (table salt and baking soda) as electrolytes.



I based my design on a project done by someone else, but they wanted didn't need to separate the Oxygen and Hydrogen, so their array was a series of alternating anode/cathode plates that were close together. His reaction was VERY energetic, and produced a lot of gas quickly.

His electrode array (1): +-+-+-+-+-
Mine (2): ++++++ -------

When applying the current, bubbles form on both electrodes, but VERY slowly. I'm wondering if the difference in effect is due to the distance the current must travel between anode and cathode. I haven't found any resources that could verify this, however.

Any insight would be appreciated.

Thanks in advance.




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[*] posted on 1-4-2008 at 11:33


That huge gap in the center is killing you. Most electrolytes are not that conductive, so there is considerable resistance in the region between electrodes; I'd bet you can measure a voltage across that open region by sticking voltmeter probes on either side.

The back side of electrodes doesn't contribute as much to current flow as the front, and electrodes hidden behind others are even less effective - the front electrode shields them to an extnt.

So remake the tank with very little gap between the two chambers, the cathode and anode should be as close together as practical. I'd use a single separator, have the solid section extended to below the electrodes using a porous membrane - non-woven plastic fabric works well. Rotate the electrode arrays 90 degrees so their plates parallel the sides of the tank; better yet make new ones that are much larger than these, reaching nearly to the bottom of the tank. Use an area behind one or both electrodes to proved access for filling the tank, instead of between them.

With ferrous alloy electrodes stick with alkaline electrolytes and avoid chlorides and other halides like the plague. Hydroxide or carbonate is better than bicarbonate.
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microcosmicus
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[*] posted on 1-4-2008 at 11:43


Quote:

I based my design on a project done by someone else, but they wanted didn't need
to separate the Oxygen and Hydrogen,


Not separating the H2 from the O2 sounds like an AWFUL
idea to me, especially on a large scale, because the mixture is
explosively flammable, so I'm glad to see you're not trying that.

Quote:

I'm wondering if the difference in effect is due to the distance the current must travel between anode and cathode. I haven't found any resources that could verify this, however.


It's just good old Ohm's law ---- the further apart the electrodes,
the greater the resistance, so the less the current and the less
gas produced. So I would suggest measuring the resistance
of your cell or the current while electrolyzing. If the current is
all that your power supply can put out, then placing the electrodes
closer together won't do much except possibly burn out your
power supply if it does not limit the current it produces. If the
current is well below what your power supply can put out, only then
consider bringing the plates closer to decrease resistance.

Quote:

When applying the current, bubbles form on both electrodes, but VERY slowly.


As for how fast the bubbles form, remember that a mole of
electrons is 26.8 amp-hours. Running at the full 10 amps your
charger is capable of will therefore produce hydrogen at the rate
of 373 mg/hr. At STP, that amounts to about a gallon of H2 in an
hour. The bubbles may be coming slowly simply because
that is all your power supply is capable of.

[Edited on 1-4-2008 by microcosmicus]
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slightlymadscience
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[*] posted on 1-4-2008 at 11:52


Quote:
Originally posted by not_important
That huge gap in the center is killing you. Most electrolytes are not that conductive, so there is considerable resistance in the region between electrodes; I'd bet you can measure a voltage across that open region by sticking voltmeter probes on either side.

The back side of electrodes doesn't contribute as much to current flow as the front, and electrodes hidden behind others are even less effective - the front electrode shields them to an extnt.

So remake the tank with very little gap between the two chambers, the cathode and anode should be as close together as practical. I'd use a single separator, have the solid section extended to below the electrodes using a porous membrane - non-woven plastic fabric works well. Rotate the electrode arrays 90 degrees so their plates parallel the sides of the tank; better yet make new ones that are much larger than these, reaching nearly to the bottom of the tank. Use an area behind one or both electrodes to proved access for filling the tank, instead of between them.

With ferrous alloy electrodes stick with alkaline electrolytes and avoid chlorides and other halides like the plague. Hydroxide or carbonate is better than bicarbonate.


Thank you for the reply! Since it's the gap that's killing me (which seemed to be the most likely culprit from my perspective), it's no wonder that the other's rig was so much more energetic - he had alternating anode and cathode plates very close together. I had also thought that the arrays would increase the reaction due to increased surface area, but since the current doesn't have a direct path (i.e. the facing portion of the electrodes are most important, like you said), it doesn't really help.

When I get to revisit this, I'll keep your advice in mind.




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[*] posted on 1-4-2008 at 11:59


Quote:
Originally posted by microcosmicus

Not separating the H2 from the O2 sounds like an AWFUL
idea to me, especially on a large scale, because the mixture is
explosively flammable, so I'm glad to see you're not trying that.


Probably for the best that you don't look at my videos/website. I tend to deliberately do a lot of ill-advised things. :P

Quote:
Originally posted by microcosmicus
the greater the resistance, so the less the current and the less
gas produced. So I would suggest measuring the resistance
of your cell or the current while electrolyzing. If the current is
all that your power supply can put out, then placing the electrodes
closer together won't do much except possibly burn out your
power supply if it does not limit the current it produces. If the
current is well below what your power supply can put out, only then
consider bringing the plates closer to decrease resistance.


One lesson I learned with this adventure is to try smaller scale versions or cheaper prototypes before I invest in a whole bunch of plexiglass and spend a bunch of time making a rig I'm not confident will work. It helped me with future demonstrations, but made me generally discouraged towards that experiment (I stoppped making videos for over 6-7 months)... I'm glad to get some good feedback this time around. Thanks.




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[*] posted on 1-4-2008 at 13:21


Tip: look at your cell from the standpoint of gaussian surfaces. The electric field created by each electrode is almost indistinguishable from a square box of the same overall dimensions. Your attempt at high surface area is in fact useless.

You really need interleaved electrodes.

Tim




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[*] posted on 1-4-2008 at 13:44


Here is a crude sketch of the electrolyser I built from stainless steel, 6mm acrylic, and non-woven polypropylene cloth. The sketch shows two series stacked cells - the one I built has 4 cells. The cunning thing about this design is that all the acrylic spacers are identical, but alternately flipped in assembly, creating a gas manifold which keeps the H an O separate.
The whole thing was stacked and glued with epoxy, and a couple of PVC pipe elbows attached to the gas manifold.
I found the best electrolyte to be NaOH. In my 4 cell stack, supplying 15A at around 20V there was sufficient H2 coming off to sustain a flame.

I should add that this setup really needs some sort of cooling loop for long term operation. Electrolysis isn't particularly efficient.
[Edited on 2-4-2008 by Twospoons]

[Edited on 2-4-2008 by Twospoons]

Electrolyser.bmp - 109kB




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smile.gif posted on 1-4-2008 at 13:56
Putting my electrolyser to good use


Here's a short vid of what happens when you ignite a foam of mixed hydrogen and oxygen (yes - inspired by "myth busters"). You could feel the shockwave slap you in the chest. Hearing protection is essential. Damn, that was a fun night.

Attachment: Hydrogen foam.wmv (951kB)
This file has been downloaded 1167 times





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[*] posted on 1-4-2008 at 14:03


hehe...great video twospoons! :) A lot of energy in those two little diatomic molecules.
I'm telling ya: not too many years from now, every car will run on water.




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[*] posted on 1-4-2008 at 18:59


Your apparatus work is looking good..
a few design quirks to tweek.

we all have old projects laying around that had issues

the PVC tube that encased this experiment melted and bent.
this suker would freely draw 100 amps
and as in twospoons video it could produce a head snapping boom

the classic issues with water electrolysis still defeat us.

so i put the electrodes close together but the gases mix
you put the electrodes far away but current draw is an issue
buying PEM's pricey

im thinking there is a palladium membrane that will let the H2 diffuse through, but block O2, this might be viable

[Edited on 2-4-2008 by roamingnome]

Electrodes.bmp - 352kB
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[*] posted on 1-4-2008 at 19:31


A palladium membrane would likely catalyse the reaction between oxygen and hydrogen - kaboom. There are membranes that would do the job but they're not that easy to come by.

Twospoons has a good solution, not only do you get the electrodes close together but you can use both sides of them as well.

NaOH is the best electrolyte, but it will absorb CO2 from the air unless protected from prolonged exposure. Sodium carbonate already has absorbed the CO2 :-) and is cheap and easy to store - your choice.
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[*] posted on 1-4-2008 at 19:40


The NaOH does have one other drawback - a tendency to produce foam. (thats not what the foam in the video is - thats detergent). Some kind of foam breaker is on my 'to do' list for the electrolyser.

Quote:
Originally posted by not_important
not only do you get the electrodes close together but you can use both sides of them as well.



Efficient material use was one of my goals with this design. Stainless and acrylic are not especially cheap materials.




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[*] posted on 2-4-2008 at 04:06


Quote:
Originally posted by Twospoons

Efficient material use was one of my goals with this design. Stainless and acrylic are not especially cheap materials.


True, but at least they're readily available. It's nice when you can get most of your materials at the local hardware store. ;)

I really appreciate all of the great replies to this. I'll definitely be revisiting this once I get some other videos (like playing with powdered magnesium) out of my queue.




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