As long as it makes a "bang" like that who gives an eff???
Reminds me of "nitro-glycerine" being an incorrect terminology...
Nobody has cared for almost 200 years right?
BTW 1 More until post 1000!!!! WoooHooo 1K!!!

PimpAssasinG wrote:no im strong but you are a fat gay mother sucker that gets raped by black man for fun
I too am extremely curious as to what the electrode material they use is.jimmy101 wrote:BTW, anyone interested in a store bought "HHO" (aagh, even Estes knows not to call it HHO) powered rocket might want to take a look at http://www.estesrockets.com/rockets.php?pid=001876
With a bit'o plumbing it could probably be used to fuel a spudgun. It's described as hydrogen fueled, which it is, but it also uses the generated O<sub>2</sub> as the oxidizer. Look up the patent for more details. The use of citric acid as the electrolyte is much safer than the often used lye or table salt. I wonder what the electrodes are made of?
PimpAssasinG wrote:no im strong but you are a fat gay mother sucker that gets raped by black man for fun
Basically, salts of the above list.The following cations have lower electrode potential than H+ and are therefore suitable for use as electrolyte cations: Li+, Rb+, K+, Cs+, Ba2+, Sr2+, Ca2+, Na+, and Mg2+. Sodium and lithium are frequently used, as they form inexpensive, soluble salts.
If an acid is used as the electrolyte, the cation is H+, and there is no competitor for the H+ created by disassociating water. The most commonly used anion is sulfate (SO42-), as it is very difficult to oxidize, with the standard potential for oxidation of this ion to the peroxodisulfate ion being −0.22 volts.
PimpAssasinG wrote:no im strong but you are a fat gay mother sucker that gets raped by black man for fun
PimpAssasinG wrote:no im strong but you are a fat gay mother sucker that gets raped by black man for fun
I wonder if it is a problem with the relative solubilities of H2 and O2 in water? If the O2 is much more soluble in water than the H2 then the water will trap a fair amount of it. Might want to google for the two solubilites. If it is a solubility problem then run the cell for a while to saturate the water with H2 and O2 then empty your collection chamber and run the cell some more. Once the water is saturated you won't loose any more O2 to it.Insomniac wrote:The second issue with my setup is that it isn't producing gasses in the right ratios. I'm pretty sure that somwhere along the line I'm losing quite a bit of oxygen. If I electronically ignite a small amount of gas in a balloon underwater and manage not to burst it, the balloon is still partly inflated afterwards. Letting this gas out over a flame results in a pale orange, fast burning flame (Ie, it doesn't have the long, bright burn of somthing like propane, it 'whooshes' as it burns). I don't know why I'm left with this gas. I'm fairly sure it's hydrogen based on the way it burns, and the only reason I'd have extra hydrogen is if there wasn't enough oxygen to burn it. I don't think it's leeching out of the balloon as I'd expect the smaller hydrogen molecule to do so at a faster rate, which would leave me with too much oxygen. My best guesses are that it's somehow oxidizing the carbon leaving me with either carbon dioxide or monoxide, or combinging with somthing in the electrolyte. However this is all wild speculation and I don't have enough chemistry knowledge to know if this is plausable or not. (I suppose the heat of the combustion could also cause the latex of the balloon to decompose into somthing flammable but that seems a bit unlikely)
I seem to recall that commercial H2 generators use nickel plated electrodes, but I could be wrong. Might just try a couple of US Nickels.Insomniac wrote:I'm interested to know if nickel would work, because if I remember correctly it's the material used in the electrolysis cell on the 'deans benchtop' water rocket site. (I found a link showing how he made it, not sure where though.)
1. People care because it is a sure sign of someone running a con job or of chemical ignorance. The "HHO" mixture has been known for a long time and has an accepted name, i.e., a 2:1 mixture of H<sub>2</sub> and O<sub>2</sub>.THUNDERLORD wrote:So what if it's "HHO" or "H2O2" Or IDK...call it "POOP"....
As long as it makes a "bang" like that who gives an eff???
Reminds me of "nitro-glycerine" being an incorrect terminology...
Nobody has cared for almost 200 years right?
See this is one of places where people make big mistakes. Yes, there is a possibility of getting detonation instead of deflagration with H2. But that doesn't change the amount of energy released only how quickly it is released. In DDT you get very high shock wave pressures but that pressure lasts for an extremely short period of time, IIRC on the order of a couple microseconds. A shock wave is typically a fairly inefficient way to transfer energy from a gas to a solid. A massive high pressure shock wave can do a lot of damage. The shock wave in a couple liter volume of H2 only puts the container at risk, it's an awful way to try to actually transfer energy to a projectile or piston. In an ICE all a shock wave ("pinging") does is setup acoustic resonances in the engine which beat the crap out'a the bearings. The short pressure spike is much too short to be of mechanical use in the engine.boyntonstu wrote:Copied from another forum and authored by a fellow 'HHO' idiot.
"First of all, with a fast initiator (like a brisant explosive charge)
and atmospheric pressure (etc.), the gasoline will win, big time. Why?
At atmospheric pressures and temperatures, gasoline vapor is much more
dense than hydrogen. Even though hydrogen has much more energy per
pound, gasoline has much more energy per unit of volume.
Now, simply a spark to ignite the mix and the hydrogen will be MUCH more
brisant, it will deflagrate or detonate with a bigger "bang" because it
has a much higher propagation velocity than gasoline. In fact, hydrogen
burns so fast, it may not need an initiator to be an FAE. If you look
at the experimental data on flame front propagation, the measurements
showed supersonic propagation of the flame front in a tube, which would
turn it from simple burning or deflagration (combustion that propagates
through a gas or along the surface of an explosive at a rapid rate
driven by the transfer of heat wordnet.princeton.edu/perl/webwn
<http>)
Yes, a slow blast like the fertilizer explosion in Oklahoma is a good example.jimmy101 wrote:See this is one of places where people make big mistakes. Yes, there is a possibility of getting detonation instead of deflagration with H2. But that doesn't change the amount of energy released only how quickly it is released. In DDT you get very high shock wave pressures but that pressure lasts for an extremely short period of time, IIRC on the order of a couple microseconds. A shock wave is typically a fairly inefficient way to transfer energy from a gas to a solid. A massive high pressure shock wave can do a lot of damage. The shock wave in a couple liter volume of H2 only puts the container at risk, it's an awful way to try to actually transfer energy to a projectile or piston. In an ICE all a shock wave ("pinging") does is setup acoustic resonances in the engine which beat the crap out'a the bearings. The short pressure spike is much too short to be of mechanical use in the engine.boyntonstu wrote:Copied from another forum and authored by a fellow 'HHO' idiot.
"First of all, with a fast initiator (like a brisant explosive charge)
and atmospheric pressure (etc.), the gasoline will win, big time. Why?
At atmospheric pressures and temperatures, gasoline vapor is much more
dense than hydrogen. Even though hydrogen has much more energy per
pound, gasoline has much more energy per unit of volume.
Now, simply a spark to ignite the mix and the hydrogen will be MUCH more
brisant, it will deflagrate or detonate with a bigger "bang" because it
has a much higher propagation velocity than gasoline. In fact, hydrogen
burns so fast, it may not need an initiator to be an FAE. If you look
at the experimental data on flame front propagation, the measurements
showed supersonic propagation of the flame front in a tube, which would
turn it from simple burning or deflagration (combustion that propagates
through a gas or along the surface of an explosive at a rapid rate
driven by the transfer of heat wordnet.princeton.edu/perl/webwn
<http>)
it could be used as a propellant and it would probably work fine but its impractical to use on a large scale. where propane and butane are both easily accessible and cheap gases that can be found virtually anywhere. so what exactly the point of tirelessly pursuing this?Yes, a slow blast like the fertilizer explosion in Oklahoma is a good example.
Would the increase in pressure caused by ignited H2 in a vessel be useful as a propellant?