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Peroxide biprop ignition

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Oren Tirosh - 01 Dec 2003 14:40 GMT
Some methods I've seen mentioned for peroxide biprop ignition are:

 Decompose the peroxide with catalyst pack.
 Pyrotechnic igniter in the chamber.
 Dissolve catalyst in fuel.
 Hypergolic starting slug in fuel feed line.

How about mixing some liquid catalyst into the peroxide feed for a few
seconds until there is stable self-sustaining combustion in the
chamber? Liquid catalysts for monoprops have been abandoned in favor
of catalyst packs for good reasons but they seem to have some
desirable properties for biprop ignition:

Usable with high concentration peroxide.
Can be used with strongly stabilized peroxide.
No hazardous materials.
Restartable and reusable.

The catalyst is mixed into the peroxide just before injection into the
chamber. This cannot be done safely with a fuel but catalytic
decomposition is slow enought to give some time for mixing. The
injector is optimized for operation with uncatalysed peroxide. It may
not perform optimally with the mixed-phase decomposing peroxide; it
just needs to be good enough for the ignition phase. The injector and
mixing chamber are flushed of any residues by ample amounts of
peroxide (except on some emergency shutdowns) so the catalyst should
not contaminate the upstream oxidizer lines .

Oren
Henry Spencer - 05 Dec 2003 19:01 GMT
>How about mixing some liquid catalyst into the peroxide feed for a few
>seconds until there is stable self-sustaining combustion in the
>chamber?

This is a minor variant of the "hypergolic starting slug" approach.

> No hazardous materials.

Depends on what catalyst you're using.  Even permanganates are not exactly
mother's milk, and things like TEA are definitely hazardous.

> Restartable and reusable.

Subject to the need for yet another fluid system, with the added
complexity that entails.

>The catalyst is mixed into the peroxide just before injection into the
>chamber. This cannot be done safely with a fuel but catalytic
>decomposition is slow enought to give some time for mixing.

I have real doubts about that part of the idea.  Catalystic decomposition
will not be slow with high-concentration peroxide and an effective liquid
catalyst mixed well together.  Mixing *in* the chamber sounds both better
and safer.
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MOST launched 30 June; first light, 29 July; 5arcsec    | Henry Spencer
pointing, 10 Sept; first science, early Oct; all well.  | henry@spsystems.net

Julian Bordas - 08 Dec 2003 16:28 GMT
>> Restartable and reusable.
>
[quoted text clipped - 9 lines]
> catalyst mixed well together.  Mixing *in* the chamber sounds both better
> and safer.

Once the rocket is firing, is it possible to use non catalysed HTP?
Henry Spencer - 08 Dec 2003 15:13 GMT
>> I have real doubts about that part of the idea.  Catalystic decomposition
>> will not be slow with high-concentration peroxide and an effective liquid
>> catalyst mixed well together.  Mixing *in* the chamber sounds both better
>> and safer.
>
>Once the rocket is firing, is it possible to use non catalysed HTP?

Yes, definitely.  As with any propellant combination, once it's lit it
will generally stay lit, modulo combustion-stability issues.  People have
built rocket engines using peroxide as oxidizer with no catalyst at all,
just a conventional ignition system.
Signature

MOST launched 30 June; first light, 29 July; 5arcsec    | Henry Spencer
pointing, 10 Sept; first science, early Oct; all well.  | henry@spsystems.net

Julian Bordas - 13 Dec 2003 11:04 GMT
>>>I have real doubts about that part of the idea.  Catalystic decomposition
>>>will not be slow with high-concentration peroxide and an effective liquid
[quoted text clipped - 7 lines]
> built rocket engines using peroxide as oxidizer with no catalyst at all,
> just a conventional ignition system.

Thanks Henry.  I'm one step closer :-)

Julian
Allen Meece - 16 Dec 2003 03:11 GMT
<<Catalystic decomposition
> will not be slow with high-concentration peroxide and an effective liquid
> catalyst mixed well together. >>
 I've only heard of solid catalyst beds. What's a [non-exotic] liquid catalyst
for HTP, [High Test Peroxide over 85% pure]?
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John Carmack - 05 Dec 2003 22:51 GMT
> Some methods I've seen mentioned for peroxide biprop ignition are:
>
[quoted text clipped - 13 lines]
>  No hazardous materials.
>  Restartable and reusable.

It could probably work, but I think you overstate the case for it.

Various platinum based catalysts will work fine with 98% peroxide, it
is only the classic silver ones that have issues.  The commercial
catalysts we are using for our mixed-monoprop engines would work fine
with 98%, for instance.

High concentration and highly stabilized is really only a condition
that happens at the amateur experimental stage where people are
concentrating cheap peroxide on bench level equipment in small
batches.  Anything resembling a commercial rocket is almost certainly
going to be using unstabilized peroxide.

Adding a third consumable and the associated plumbing is a non-trivial
increase in system complexity.

We have only done a few tests with liquid catalysts, but we have had
much better success with solid catalyst packs.  Compared to almost any
other biprop, cat-pack decomposition auto-ignition biprops are really
easy to make work at good efficiencies.

John Carmack
www.armadilloaerospace.com
Derek Lyons - 06 Dec 2003 01:01 GMT
>High concentration and highly stabilized is really only a condition
>that happens at the amateur experimental stage where people are
>concentrating cheap peroxide on bench level equipment in small
>batches.  Anything resembling a commercial rocket is almost certainly
>going to be using unstabilized peroxide.

Why is this so may I ask?

D.
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Henry Spencer - 06 Dec 2003 03:47 GMT
>>High concentration and highly stabilized is really only a condition
>>that happens at the amateur experimental stage where people are
[quoted text clipped - 3 lines]
>
>Why is this so may I ask?

A commercial rocket is going to be using peroxide in sufficient quantity
to get reasonable cooperation from peroxide suppliers (from new ones
created to serve it, if not from existing ones).  So it will have access
to high-concentration peroxide that is either unstabilized or, at worst,
lightly stabilized.

Whereas amateurs have to work with existing peroxide suppliers, who are
unhelpful (to put it mildly).  So they are likely to have to do their own
concentrating, and most of the easy bench-scale processes concentrate
stabilizers as well as peroxide.

Back when Beal was a going concern, buying high-concentration unstabilized
peroxide in quantity and gearing up to buy it in QUANTITY, for a little
while amateurs could piggyback on that new peroxide infrastructure and buy
small amounts of rocket-grade peroxide without much difficulty.  Not any
more, as John can tell you at some length.
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MOST launched 30 June; first light, 29 July; 5arcsec    | Henry Spencer
pointing, 10 Sept; first science, early Oct; all well.  | henry@spsystems.net

Oren Tirosh - 06 Dec 2003 11:20 GMT
Thanks Henry, John.

All else being equal, would you not prefer your 98% peroxide
stabilized? After all, stabilizers are not added by manufacturers to
make life harder for rocket builders. They are supposed to make
peroxide safer. You've explained why all else is not exactly equal but
the bottom line is a tradeoff between complexity perceived safety.
Such perceptions are not an exact science and are liable to change
quickly on certain circumstances.

Oren
Henry Spencer - 06 Dec 2003 22:39 GMT
>All else being equal, would you not prefer your 98% peroxide
>stabilized? After all, stabilizers are not added by manufacturers to
>make life harder for rocket builders. They are supposed to make
>peroxide safer.

It's actually more a matter of making it less prone to deteriorate due to
contamination, and giving it a longer shelf life.  I can't speak for John,
but if I were doing peroxide rocketry, I'd be willing to accept
constraints like a short shelf life and a need to be fussy about
cleanliness, in return for less hassle with catalyst poisoning etc.

All else being equal, yes, I'd be happier with *lightly* stabilized
peroxide using stabilizers compatible with my catalysts.  (There is some
choice about just which stabilizers are used, and if you're buying in
bulk,  you should have some voice in that decision.)  The less fussy I have
to be about procedural details like cleaning and shelf life, the more time
and effort I can spend on design and development problems.

But there are a lot of assumptions in that (e.g, *are* there such
stabilizers?) and just getting it unstabilized might well be less hassle
all around.
Signature

MOST launched 30 June; first light, 29 July; 5arcsec    | Henry Spencer
pointing, 10 Sept; first science, early Oct; all well.  | henry@spsystems.net

 
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