bootlegin
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hho electrolysis plate configuration
Hi! I'm currently attempting to build an electrolysis chamber for the production of hho to power one of those old 30's prest-o-lite air acetylene
torches. I've thought of two different plate configurations I could use but am stuck deciding which one. Ive included a drawing of the two
configurations I'm talking about.
Type 1 has more surface area on a single electrode and requires low volage/high current. Type 2 has less surface area and requires high voltage/low
current. Type 1 is similar to the plate configuration of a cell within a lead acid battery. Type 2 seems to be the more commonly used configuration.
I actually have another question, this one regarding plate material. Would it be feasible to reuse the plates from dead car batteries as electrolysis
plates? looking around on these forums, it seems that PbO is a good material for this and I have a ton of them in a box, most of them being in really
good condition still.
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Sulaiman
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Usually type2 is used when a power supply is N.Vcell, eg 12Vdc supply
As you have many plates available you could make N.(type1) cells electrically in series.
It all depends upon desired production rate, available materials and power supply voltage and current
Don't forget to add some type of flame arrestor to prevent explosion of your cell(s)
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Junk_Enginerd
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How your plates should be configured is driven by the voltage of the power supply you're planning to use. Between 2-3 volts per gap is a good rule of
thumb.
Powering a flame with HHO requires obscene amounts of electricity. The highest power I've run was 1500 W and the flame produced by that was laughably
small. Very hot, but cigarette lighter sized. An ordinary medium sized propane torch is at least 5 kW, and due to the inherent inefficiency of
electrolysis you only get at most 60% flame power vs input power.
Due to the very high power, running at low voltage is impractical; you'd need massive cables, think several hundreds of mm2, and you'd lose lots of
power to resistance anyway.
From that perspective, you should use as high voltage as possible and therefore as many cells/gaps as possible.
However, as voltage increases so does the personal safety risk. Up to 80 VDC or so is fine from a safety point of view, after that it becomes
necessary to either insulate or be very cautious around the thing.
With increasing voltage comes increasing complexity as well. Sure, 10 cells is no big deal, but 100 cells may be a little unreasonable depending on
how you design and build it.
Somewhere inbetween those ends is a comfortable compromise for you, and exactly where only you can say.
I don't know how lead plates would work, but I do recommend that you use stainless steel. Using sodium hydroxide as an electrolyte, stainless steel is
almost entirely unaffected, and you don't need to consider any toxicity.
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Parakeet
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Quote: Originally posted by Junk_Enginerd  | | I don't know how lead plates would work, but I do recommend that you use stainless steel. Using sodium hydroxide as an electrolyte, stainless steel is
almost entirely unaffected, and you don't need to consider any toxicity. |
Can I really use stainless steel as an anode? Doesn’t it dissolve and form hydroxides?
Fe —>Fe3++e-
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Rainwater
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Just as a "what the hell" i onced cut slots into a 1in diameter pcv pipe and arranged 60 washers. Inserted that into a 1.5in pvc with caps and a vinyl
tube.
Then filled the pipe with water Hooked it directly to mains with a current meter.
Then added 2 or 3 grains of NaOH at a time until gas started being produced.
Worked like a champ until it got to hot.
Id give this one an 8/10 on the meet-yo-maker meter
"You can't do that" - challenge accepted
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JohnnyBuckminster
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I built a small cell with electrodes of steel (4 cm x 4 cm) and water/NaOH as electrolyte.
It did not work.
After a short runtime, less than 5 minutes, the electrode showed
severe signs of corrosion, and the electrolyte became brownish and warm.
I used a 6 V battery as a power source (well above the standard potential for electrolysis of water 1.3 V, so excess heat).
Replacing NaOH with KOH reduced the corrosion,
but it was still quite significant.
So I replaced the electrodes with 304 stainless steel,
which basically eleminated the problem with corrosion.
So, steel no, but stainless steel 304 yes.
[Edited on 2022-12-28 by JohnnyBuckminster]
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Twospoons
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I built a four plate version of type 2 using stainless steel and strong NaOH soln. Worked very well - with 20A flowing it would sustain a flame
(hydrogen/air) on the end of a 20mm tube.
I had gas separators in mine so the H2 and O2 weren't mixed until I wanted them to. And if you've seen a bag full of H2/O2 mix ignited you will know
why ( hearing protection is mandatory). Make sure you have damn good flame arrestors on your gas torch.
Best results require a large area, small spacing and reasonably concentrated electrolyte.
Helicopter: "helico" -> spiral, "pter" -> with wings
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JohnnyBuckminster
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Quote: Originally posted by Twospoons  | I built a four plate version of type 2 using stainless steel and strong NaOH soln. Worked very well - with 20A flowing it would sustain a flame
(hydrogen/air) on the end of a 20mm tube.
I had gas separators in mine so the H2 and O2 weren't mixed until I wanted them to. And if you've seen a bag full of H2/O2 mix ignited you will know
why ( hearing protection is mandatory). Make sure you have damn good flame arrestors on your gas torch.
Best results require a large area, small spacing and reasonably concentrated electrolyte. |
My plan was to generate green H2(g) with a portable 12 V solar panel. As it turned out, PEM membranes, I purchased Nafion from FuelCellStore, are
expensive. I, therefore, scaled down everything and built a prototype using a 6V battery with two plates according to @bootlegin type 2.
I could generate some H2/O2, but it is not as easy as it might appear in some YouTube videos. When I reduced the distance between the plates, using
rubber gaskets as spacers, it got increasingly difficult to keep the gases separated, and also, I suspect there was a build-up of gas between the
plates that got stuck. So, some sort of circulation of the electrolyte is probably necessary. I didn't want to go too high in electrolyte
concentration but stay in the safe zone for the long-term survival of the membrane. Everything was quite leaky, and I never took it any further.
@Twospoons, What type of membrane did you use, how strong was the electrolyte, and how did you extract the generated H2 and O2 gases
from the individual chambers?
[Edited on 2022-12-29 by JohnnyBuckminster]
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Admagistr
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Quote: Originally posted by Twospoons  | I built a four plate version of type 2 using stainless steel and strong NaOH soln. Worked very well - with 20A flowing it would sustain a flame
(hydrogen/air) on the end of a 20mm tube.
I had gas separators in mine so the H2 and O2 weren't mixed until I wanted them to. And if you've seen a bag full of H2/O2 mix ignited you will know
why ( hearing protection is mandatory). Make sure you have damn good flame arrestors on your gas torch.
Best results require a large area, small spacing and reasonably concentrated electrolyte. |
Hi,Iam also building an electrolytic device for oxygen-hydrogen flame,but not HHO,oxygen and hydrogen separately.Do you have the results of your work
somewhere,so I can be inspired ?For inspiration:
https://www.aliexpress.com/item/1005003247319732.html
https://www.aliexpress.com/i/4001192601347.html
https://www.youtube.com/watch?v=gZJEDe_HUcw
https://www.youtube.com/watch?v=gH-jhN3mV60
https://www.aliexpress.com/item/1005003726628551.html
https://www.fuelcellstore.com/electrolyzer-10-e102
HHO:
https://www.enginediy.com/products/electrolysis-of-water-gen...
[Edited on 29-12-2022 by Admagistr]
[Edited on 29-12-2022 by Admagistr]
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Junk_Enginerd
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Yes, if the electrolyte is sodium hydroxide it is almost completely unaffected. All I've noted is a very minor color shift towards darker, after
several hours of 100+ Amps.
If the anode was Iron as in you formula, then yes, it would. But it's not iron, it's stainless steel. Looking at chromium or nickel would be more
accurate.
Quote: Originally posted by Rainwater  | Just as a "what the hell" i onced cut slots into a 1in diameter pcv pipe and arranged 60 washers. Inserted that into a 1.5in pvc with caps and a vinyl
tube.
Then filled the pipe with water Hooked it directly to mains with a current meter.
Then added 2 or 3 grains of NaOH at a time until gas started being produced.
Worked like a champ until it got to hot.
Id give this one an 8/10 on the meet-yo-maker meter |
'the hell
I deeply respect your jank-level. But... No rectifier? Not much hho production with AC.
On a more serious note, cooling is really an issue on higher power cells. Mine was about 1500 W input, and efficiency is probably 50% at best. 750 W
in a mostly closed system gets hot fast.
[Edited on 29-12-2022 by Junk_Enginerd]
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Twospoons
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Quote: Originally posted by JohnnyBuckminster  |
@Twospoons, What type of membrane did you use, how strong was the electrolyte, and how did you extract the generated H2 and O2 gases
from the individual chambers?
|
Membrane was non-woven polypropylene cloth - the type used for weed matting and cheap shopping bags. Gas extraction was via a manifold formed in the
the cell spacers, which were 6mm acrylic with cutouts as per attached image - alternating spacers were flipped left-right.
The whole stack was built up : ss plate | left spacer | membrane | right spacer| plate | left spacer | membrane etc.
There was also a small hole right at the bottom through the whole stack to allow the electrolyte level to equalize across all the cells.
Don't know the electrolyte concentration, I just tossed some NaOH in some water without measuring.

Here it is in operation
Fridays after work was always beer and science (not always the best mix)
[Edited on 29-12-2022 by Twospoons]
Helicopter: "helico" -> spiral, "pter" -> with wings
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Junk_Enginerd
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Clever and simple design. One thing that stopped me from trying a separated output cell like this was pressure. You'll be getting twice the volume of
H2 gas compared to O2 gas, right? That means the pressure between the O2 and H2 cells will naturally be unbalanced, and the O2 is at risk of being
contaminated by H2. Cloth will stop gas transfer, but not if there's any pressure behind it.
What with the VERY generous explosive limits of hydrogen concentration in oxygen, I feel like I'd never be able to trust the oxygen at least anywhere
near a flame.
Did you notice any such problems?
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Twospoons
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I only tried to fill balloons once. That ended badly when one balloon slipped off and the other forced electrolyte through the cell, out the other
tube, and showered the lab and me.
You can collect gas in a plastic bag though - no back pressure.
Watch the video in the link above : we were goofing off after work, tried igniting hydrogen alone (tame) and also stoichiometric H2/O2 mix (scary).
Helicopter: "helico" -> spiral, "pter" -> with wings
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JohnnyBuckminster
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Quote: Originally posted by Twospoons  | Quote: Originally posted by JohnnyBuckminster  |
@Twospoons, What type of membrane did you use, how strong was the electrolyte, and how did you extract the generated H2 and O2 gases
from the individual chambers?
|
Membrane was non-woven polypropylene cloth - the type used for weed matting and cheap shopping bags. Gas extraction was via a manifold formed in the
the cell spacers, which were 6mm acrylic with cutouts as per attached image - alternating spacers were flipped left-right.
The whole stack was built up : ss plate | left spacer | membrane | right spacer| plate | left spacer | membrane etc.
There was also a small hole right at the bottom through the whole stack to allow the electrolyte level to equalize across all the cells.
Don't know the electrolyte concentration, I just tossed some NaOH in some water without measuring.
Here it is in operation
Fridays after work was always beer and science (not always the best mix)
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Impressive! I will be back in the garage and build a new one along this idea... of course, this is the way to get the H2 and O2 out, it looks obvious
now... I did something completely different... cheers
[Edited on 2022-12-30 by JohnnyBuckminster]
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Parakeet
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Sorry if this question is off topic.
I have a solution of sodium hydroxide, which I want to concentrate and get solid crystals. The straightforward way is to heat the solution and
evaporate the water, but sodium hydroxide solution can dissolve glass. Of course I can use a metal container, but I will have to deal with scary hot
boiling sodium hydroxide solution.
So what I thought of is, can I concentrate this solution by electrolysis? Water should become hydrogen and oxygen, while sodium hydroxide remains. Is
this a silly idea?
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Sulaiman
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Get a cheap stove (electric, gas, charcoal etc) and boil down the solution to dryness.
Do it outdoors, stay far away and/or upwind, use an iron, steel or stainless steel pan.
Definitely not aluminium.
This will give a crystaline mass of sodium hydroxide.
I've no idea how to get large crystals.
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Junk_Enginerd
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Quote: Originally posted by Parakeet  | Sorry if this question is off topic.
I have a solution of sodium hydroxide, which I want to concentrate and get solid crystals. The straightforward way is to heat the solution and
evaporate the water, but sodium hydroxide solution can dissolve glass. Of course I can use a metal container, but I will have to deal with scary hot
boiling sodium hydroxide solution.
So what I thought of is, can I concentrate this solution by electrolysis? Water should become hydrogen and oxygen, while sodium hydroxide remains. Is
this a silly idea? |
If you just want to get rid of the water, simmer it in a normal kitchen stainless steel pot. Piece of cake. That will produce a dry powder, or melt
into a difficult cake if you heat it too much.
If you want to get rid of water and don't want the scary boiling issue, set it on the stove, in a pot, at the lowest heat and point a fan at it. It'll
dry out fairly quickly, and won't spatter and misbehave.
If you want bigger crystals, just make a saturated solution and leave it alone in a jar for a while. It'll evaporate and crystallize on its own,
assuming you're not in some tropical humid place. It won't affect the glass significantly if it's at room temperature, but maybe do it with glassware
you're not super attached to, like some old mason jar, just in case it gets weakened.
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Parakeet
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Thanks for your comments.
I now realized that electrolysis requires a lot of energy, probably more than just boiling it off. Okay, I will just heat the solution.
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Mateo_swe
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Junk_Enginerd, you said you used at maximum 1500W and the flame produced by that was laughably small.
There surely must be a more effective way to make the splitting of the molecule, was your cell constructed without any thought of effectiveness or
optimizations done?
I have not tried this myself on any larger scale so i might be mistaken but i have seen videos of HHO cells that produce quite high volume of HHO gas.
Using 1500watts one must be able to make a decent torch at least, or is this process so inefficient?
If one is interested in HHO generators and splitting the water molecule there is one interesting source of documents and that's the supposedly
invented "Water powered sand-Buggy" built by Stanley A Meyer.
Now, i don't think for one moment that his patents and drawings can make a HHO unit that are able to power a car as he claimed, but his HHO units did
produce very much HHO gas.
If one look at the patents (i include one of those patents) and documents about it he really did a lot of work to try figure out how to split the
water molecule in the most efficient way.
Water powered car, nah, i dont think so.
But good and effective HHO generators, sure i can believe that after looking at some of his designs.
He did die under some suspicious circumstances, maybe there was a grain of thruth in his claims.
There is also a lot of good info regarding HHO generators on the net if you filter off the "Perpetual motion lunatics" and look at the more science
based info.
Maybe i should build me a HHO generator, it would be both fun and interesting.
I got most materials and a high temperature HHO torch might be good to have for something some day.
Attachment: US4936961.pdf (615kB) This file has been downloaded 409 times
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Twospoons
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Without appropriate catalytic electrodes water splitting is only ~50% efficient, (from memory - dont quote me!). Add in the losses in the electrolyte
resistance, especially in a sub-optimal geometry, and the efficiency could be pretty bad.
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Junk_Enginerd
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Quote: Originally posted by Mateo_swe  | Junk_Enginerd, you said you used at maximum 1500W and the flame produced by that was laughably small.
There surely must be a more effective way to make the splitting of the molecule, was your cell constructed without any thought of effectiveness or
optimizations done?
Using 1500watts one must be able to make a decent torch at least, or is this process so inefficient?
|
I can't begin to guess at the efficiency om my cell, but I don't think it was much worse than most electrolysis processes. The thing is that fire is
pretty energetic(duh). A normal $20 propane/butane torch that runs off disposable bottles is something like 3-6 kW, and they're not too impressive
really. An ordinary cigarette lighter is around 100 W.
50% efficiency is good when it comes to electrolysis. I think the theoretical maximum efficiency is about 60%.
So, to even match a normal random propane torch, we're realistically looking at minimum 6-12 kW of input power. That's approaching the limit of what a
normal household electric installation can even handle.
My setup could peak at around 2.5 kW input for shorter amounts of time, before the electrolyte started boiling off and the fuse popped. At that point
I got an angry little flame which was perhaps 4 mm across, though probably 5 cm long. Very narrow and very hot, and almost invisible
except for the sodium contamination tinting it a little orange.
Pointing it at a standard glass bottle, it would melt a 4 mm hole in a few seconds clean through. It would also deliver heat fast enough to melt
steel. Too bad you can't weld with it since both oxygen and hydrogen are the biggest enemies to steel welds lol.
It was useless for heating anything large though, since again, the total power output of it wasn't really that impressive. The contrast between the
high heat and low power was weird in that, as stated above, it would happily melt steel, but if you pointed it at an aluminium part almost nothing
happened since it conducted away the heat so much faster.
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MrDoctor
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i want to try something like this, though i need to seperate the H2/O2 since i also want to be able to use them individually, esp pure O2 for contact
process without having to buy O2. Free power is also great for making nitric acid, or ozone, both of which also benefit from pure O2.
While it may seem silly, i realized a great way to get huge amounts of power beyond what you can usually get from the wall, especially when you need
to step it down then, is to use solar panels. 3-4 good panels will output 1kw, 6-8 2kw. for around $50-70 you can get MPPTs which can spit out 36 or
48v at 700-1200W, from a few panels up to an open-voltage of around 150V. you do though need to get the higher voltage options for efficiency as they
are current limited, so 48V is ideal, 4x car batteries as a power buffer.
4x of the MPPTs, 16x panels, gets you to over 4kW max continuous during the day, though since you have 4x car batteries, even old dying ones will be
able to crank out extra power for a quick boost, consuming both battery charge and available solar, as long as you add balancers and stick low voltage
breakers on each battery. you can also just have the whole thing supplementing your mains powered base system too to crank out more, and on that note,
a 2.5kW SMPS + 4x batteries for a 48V HHO, could probably spit out 8-10kW for a minute or two, with a duty cycle of 20%
collecting 16 solar panels for cheap or free is actually not very difficult, i have over 20 of them i pick up now and then, and since the MPPT tank is
limited to 3-4 panels while staying economical, it wont matter that your groups dont match one another since its all parallel out. solar panels for
rooftops are 25-42v, wheras super expensive camping panels are 12v or 24v. rooftop panels are not worth much, a wholesaler i looked up prior to covid
sold them at $48ea for 250W panels when bought in lots of 8 or more. Thats the people supplying the solar rooftop install companies. i see them for
sale after warranty replacements of the entire system, for $5-10ea in the local classifieds.
Lastly, nickle cathodes, and possibly also anodes, improve efficiency as they are catalytically active, though obv not as much as platinum group
metals. But you are free to try plating the anodes/anode sides, with exotic substances that might improve the cell efficiency a bit, without much
consequence if it corrodes away as the nickle or SS base is inert here.
Im pretty sure using either long, or just thin tubing, you can make a sort of overflow manifold so that the cells all balance their electrolytes into
each other and allow you to flow it through so theres no localized heat buildup, while mitigating significant current leak, a small cut in efficiency
for more raw power output.
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Sulaiman
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thoughts ........
solar panels appear to me to be a viable source of d.c. power suitable for electrolysis,
- while direct sunshine reaches the panels.
storing or accumulating large volumes of HHO is INSANE !
I guess that drying, compressing and cooling hydrogen and oxygen for storage would use a lot of power,
for hydrogen storage you could make a few mini-Hindenburgs
Ensuring that hydrogen and oxygen never mix offers a few challenges.
Sorry, I am quite negative on this use of solar panels,
but if you have panels, controller batteries etc. then experimenting would be fun,
the idea of kilowatts of electrolysis with a diy setup sounds more hazardous than moonshine production.
As a diy water electrolysis system is unlikely to be safe enough to run unattended,
automatic control systems are not really required.
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MrDoctor
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going over 100A probably isnt the best idea for a DIY HHO array, after 20A its probably time to build more individual units.
For hydrogen storage, sodium oxide forms a reversible equilibrium of sorts turning into NaH/NaOH, which behaves really weird as it dissociates. but
iirc, there was a point where at half its capacity, so 20/30 out of a maximum of 50% hydride, pressure below 30PSI could charge it up to 20-30%, and
you had to heat it so it would decompose, but only up to 150 or 175C, i was more concerned about the conditions of producing a hydride than using it
as hydrogen storage, i mainly just recall thinking that a completely plastic compressor setup, even a peristaltic pump with the hose looped around the
roller a few times, could manage pressure beyond 30PSI.
I think if subject to vacuum, when its an intimate mixture of hydride, hydroxide and oxide, some of its decomp temp band resides either below room
temp or below 100C, but i dont remember if thats at high conc NaH or low conc. its still crazy that oxide hydrogenates so easily once its doped with a
minimal amount of hydride.
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