Author Topic: Cyclic ozone (trioxirane) as oxidizer?  (Read 1692 times)

Offline zubenelgenubi

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Cyclic ozone (trioxirane) as oxidizer?
« on: 04/06/2025 06:21 pm »
Has any public source progress been made to synthesize cyclic ozone, a.k.a. trioxirane?  (O3 as an equilateral triangle)

I found this article from 2005:
Science Daily, 8 February 2005, Temple University
https://www.sciencedaily.com/releases/2005/02/050205122519.htm
Quote
Summary:
With nearly twice the energy of normal, bent-shaped ozone (O3), cyclic ozone could hold the key component for a future manned-mission to Mars. No one has ever seen-let alone made-cyclic ozone. But that could all change at Temple University's Center for Advanced Photonics Research, which has been awarded a one-year, $1.25 million grant to develop cyclic ozone by the Defense Advanced Research Projects Administration (DARPA).

I also found a few mentions here in the forum from years ago.
« Last Edit: 04/06/2025 06:23 pm by zubenelgenubi »
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Offline StraumliBlight

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #1 on: 04/06/2025 08:16 pm »
This 2024 paper (Fullerene-encapsulated Cyclic Ozone for the Next Generation of Nano-sized Propellants via Quantum Computation) suggests that "a detailed quantum computation of this problem could require millions of physical qubits and operational times extending into multiple years".

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While practical efforts to capture this isomer have been unsuccessful, it is possible that cyclic ozone would be stabilized in confined geometries. The required synthetic methods are nonetheless difficult to design and require theory–driven inputs that lie beyond the scope of classical methods. Quantum computation has the potential to enable these calculations, though the underlying hardware requirements remain unclear for many practical applications.

https://library.sciencemadness.org/library/books/ignition.pdf

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The future of ozone doesn't look so promising. Or, to be precise, ozone has been promising for years and years but hasn't been delivering.

Ozone, O3, is an allotropic form of oxygen. It's a colorless gas, or if it's cold enough, a beautiful deep blue liquid or solid. It's manufactured commercially (it's useful in water purification and the like) by the Welsbach process which involves an electrical glow discharge in a stream of oxygen. What makes it attractive as a propellant is that (1) its liquid density is considerably higher than that of liquid oxygen, and (2) when a mole of it decomposes to oxygen during combustion it gives off 34 kilocalories of energy, which will boost your performance correspondingly. Sanger was interested in it in the 30's, and the interest has endured to the present. In the face of considerable disillusionment.

For it has its drawbacks. The least of these is that it's at least as toxic as fluorine. (People who speak of the invigorating odor of ozone have never met a real concentration of it!) Much more important is the fact that it's unstable — murderously so. At the slightest provocation and sometimes for no apparent reason, it may revert explosively to oxygen. And this reversion is catalyzed by water, chlorine, metal oxides, alkalis —and by, apparently, certain substances which have not been identified. Compared to ozone, hydrogen peroxide has the sensitivity of a heavyweight wrestler.

Since pure ozone was so lethal, work was concentrated on solutions of ozone in oxygen, which could be expected to be less dangerous. The organizations most involved were the Forrestal Laboratories of Princeton University, the Armour Research Institute, and the Air Reduction Co. Work started in the early 50's, and has continued, on and off, ever since.

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #2 on: 04/07/2025 02:12 am »
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Since pure ozone was so lethal, work was concentrated on solutions of ozone in oxygen, which could be expected to be less dangerous. The organizations most involved were the Forrestal Laboratories of Princeton University, the Armour Research Institute, and the Air Reduction Co. Work started in the early 50's, and has continued, on and off, ever since.

I guess you'd call that "ozone-enriched oxygen"?? ???

Sounds promising.., but only if you can find a lab willing to work out exactly how enriched you could get your oxidiser mix before it explodes.
« Last Edit: 04/07/2025 02:14 am by zubenelgenubi »
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Offline tenkendojo

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #3 on: 04/13/2025 07:12 pm »
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Since pure ozone was so lethal, work was concentrated on solutions of ozone in oxygen, which could be expected to be less dangerous. The organizations most involved were the Forrestal Laboratories of Princeton University, the Armour Research Institute, and the Air Reduction Co. Work started in the early 50's, and has continued, on and off, ever since.

I guess you'd call that "ozone-enriched oxygen"?? ???

Sounds promising.., but only if you can find a lab willing to work out exactly how enriched you could get your oxidiser mix before it explodes.

Hydrazine and hypergolic propellants are pretty lethal alright, and we've been using them as rocket propellants for 70+ years. The biggest barrier would be producing it at economically viable level.

Offline Skye

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #4 on: 04/22/2025 01:00 pm »
Diff is, hydrazine / hypergolics don’t explode for (seemingly) no reason. Even ozone-enriched O2 is bad. In the pipes after shutdown, the o2 and ozone would deposit, and the oxygen-rich ozone would evaporate first, leaving behind ozone-rich oxygen. Really nasty. And the o2 / o3 mixture didn’t even have that much better performance than straight o2. My opinion is never use ozone, or anything containing much ozone at all.
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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #5 on: 04/22/2025 06:27 pm »
what if one could devise a high volume high speed ozone generator say post pre-burner?  (e.g. using electricity from a generator driven off the pump shaft).

Basically a way of pumping more potential energy in per unit volume (mass) of oxidizer, with the goal of getting the chamber temperature to be even hotter.  Assuming it doesn't go melty, if you can get another 1000K out of say methalox you'd get about 13% more Isp, or almost a km/sec added out of a typical MR of 7.4.

You'd flush it with straight LO2 towards the end of the burn, flushing all the ozone out of it, leaving the system safe.  The ozone would only exist in high volume flow and at no other state of the system.

Offline Twark_Main

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #6 on: 04/22/2025 07:59 pm »
what if one could devise a high volume high speed ozone generator say post pre-burner?  (e.g. using electricity from a generator driven off the pump shaft).

Might as well just use a resistive pre-heater.


Basically a way of pumping more potential energy in per unit volume (mass) of oxidizer, with the goal of getting the chamber temperature to be even hotter.  Assuming it doesn't go melty...

Chemical rockets are already fuel-rich to manage combustion temperatures.  If you could somehow accommodate higher temperatures, you would just bring the ratio closer to stiochiometric (in the pre-burners) or to the peak Isp ratio (in the main chamber, different mainly because of exhaust molecular weight).

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #7 on: 04/22/2025 09:11 pm »
what if one could devise a high volume high speed ozone generator say post pre-burner?  (e.g. using electricity from a generator driven off the pump shaft).

Might as well just use a resistive pre-heater.


Basically a way of pumping more potential energy in per unit volume (mass) of oxidizer, with the goal of getting the chamber temperature to be even hotter.  Assuming it doesn't go melty...

Chemical rockets are already fuel-rich to manage combustion temperatures.  If you could somehow accommodate higher temperatures, you would just bring the ratio closer to stiochiometric (in the pre-burners) or to the peak Isp ratio (in the main chamber, different mainly because of exhaust molecular weight).

I'm not convinced that temperature is the main blocking problem.  A lot (all?) of the off-from-stoichometric added fuel is film cooling, and that's with reasonably low molecular weight CH4.  You'd use even more film cooling if your combustion temperature were 4700K instead of the present 3700K.   So the "managed" part is a geometry problem, it's not there to keep the hottest part any cooler.    The adiabatic temperature of stoich methalox burning is 3200K, the other 500k is from high pressure used.  IOTW, Raptor has maxed out the temperature already, it's not "reduced" by non-stoich mix.

The main problem is coming up with the cyclic ozone (or even just plain ozone) safely and efficiently, on a few hundred kg/sec of oxygen flow.   I suspect it's not possible, but maybe it's worth exploring (if this thread has any worth at all).

Offline Twark_Main

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #8 on: 04/22/2025 09:58 pm »
what if one could devise a high volume high speed ozone generator say post pre-burner?  (e.g. using electricity from a generator driven off the pump shaft).

Might as well just use a resistive pre-heater.


Basically a way of pumping more potential energy in per unit volume (mass) of oxidizer, with the goal of getting the chamber temperature to be even hotter.  Assuming it doesn't go melty...

Chemical rockets are already fuel-rich to manage combustion temperatures.  If you could somehow accommodate higher temperatures, you would just bring the ratio closer to stiochiometric (in the pre-burners) or to the peak Isp ratio (in the main chamber, different mainly because of exhaust molecular weight).

I'm not convinced that temperature is the main blocking problem.  A lot (all?) of the off-from-stoichometric added fuel is film cooling, and that's with reasonably low molecular weight CH4.  You'd use even more film cooling if your combustion temperature were 4700K instead of the present 3700K.   So the "managed" part is a geometry problem, it's not there to keep the hottest part any cooler.    The adiabatic temperature of stoich methalox burning is 3200K, the other 500k is from high pressure used.  IOTW, Raptor has maxed out the temperature already, it's not "reduced" by non-stoich mix.

The main problem is coming up with the cyclic ozone (or even just plain ozone) safely and efficiently, on a few hundred kg/sec of oxygen flow.   I suspect it's not possible, but maybe it's worth exploring (if this thread has any worth at all).

So we're back to "might as well just use a resistive pre-heater."   ;)

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #9 on: 04/22/2025 10:37 pm »
what if one could devise a high volume high speed ozone generator say post pre-burner?  (e.g. using electricity from a generator driven off the pump shaft).

Might as well just use a resistive pre-heater.


Basically a way of pumping more potential energy in per unit volume (mass) of oxidizer, with the goal of getting the chamber temperature to be even hotter.  Assuming it doesn't go melty...

Chemical rockets are already fuel-rich to manage combustion temperatures.  If you could somehow accommodate higher temperatures, you would just bring the ratio closer to stiochiometric (in the pre-burners) or to the peak Isp ratio (in the main chamber, different mainly because of exhaust molecular weight).

I'm not convinced that temperature is the main blocking problem.  A lot (all?) of the off-from-stoichometric added fuel is film cooling, and that's with reasonably low molecular weight CH4.  You'd use even more film cooling if your combustion temperature were 4700K instead of the present 3700K.   So the "managed" part is a geometry problem, it's not there to keep the hottest part any cooler.    The adiabatic temperature of stoich methalox burning is 3200K, the other 500k is from high pressure used.  IOTW, Raptor has maxed out the temperature already, it's not "reduced" by non-stoich mix.

The main problem is coming up with the cyclic ozone (or even just plain ozone) safely and efficiently, on a few hundred kg/sec of oxygen flow.   I suspect it's not possible, but maybe it's worth exploring (if this thread has any worth at all).

So we're back to "might as well just use a resistive pre-heater."   ;)


Sure but that'd be OT. in this case we are trying to increase the chemical potential energy of our oxidizer (or stretching it a bit the fuel).

I don't think it's possible, the half life of O3 and cyclic O3 is far too short to even last between the mixing area and the combustion chamber, especially at the temperature/pressures being run in modern rockets.  It'll blow up your fuel pump.  Also, the known processes for generating it are only 20% efficient, the 80% will be heat, which will decrease the half life even further.

So I guess, in the end, it'll be preheating no matter how you try to keep the energy in molecular bonds.

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #10 on: 04/22/2025 10:59 pm »
what if one could devise a high volume high speed ozone generator say post pre-burner?  (e.g. using electricity from a generator driven off the pump shaft).

Might as well just use a resistive pre-heater.

Just a passing thought before this thread dies naturally:  If creation of O3 is of any benefit at all, would an electric sparkler be a more 'efficient' use of electricity than a resistive pre-heater?
 
With sufficient thrust, pigs fly just fine - however, this is not necessarily a good idea. It is hard to be sure where they are
going to land, and it could be dangerous sitting under them as they fly overhead.

Offline cdebuhr

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Re: Cyclic ozone (trioxirane) as oxidizer?
« Reply #11 on: 04/23/2025 02:17 am »
If the use of ozone is of any benefit, that energy has to come from somewhere.  This is logically equivalent to a H2/O2 engine fed from a high speed electrolyzer, with the electrolyzer powered by a generator run by the pump shaft.  I shouldn't have to explain why that wouldn't work.

I hate conservation laws.

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