chloric1
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A word on Chlorine dioxide
Ok I have read numerous post on chlorates, perchlorates and the free acids. I was especially intrigued by use of ClO2 with hot water for HClO4 . I
believe this could be done effectively and safely considering a few safety measures. First the MSDS for Chlorine Dioxide stated you do NOT want to
use more than 100mmHg partial pressure. What this means that you should use an inert carrier such as filtered air or CO2. Secondly you do not want
ClO2 to contact organics. ![:o](./images/smilies/shocked.gif)
I have taken an interest in this gas lately as I do have 2 Kg of KClO3 to mess with. I have only messed with test tube quantities because I have
neigbors quite close to me. But the methods I have used so far are safe reliable
and productive. First take potassium chlorate powder and mix this with approximate equal oxalic acid and add sufficient battery acid(H2SO4) to cover
becuase this will generate your chloric acid in solution. next prepare a hot water bath of at least 75 C. then immerse your concotion(in glass tube)
into water bath and the gas will be given off along with CO2. you could buble this into water to make acids or into ice cold BaOH H2O2 mix to make
Barium chlorite. Since KClO3 is of limited solubility only the chlorate reacting will dissolve until the decomp of the oxalic aicd is complete. The
gas is MUCH heavier than air and tend to remain in the flask?tube so you should bubble CO2 gently in to force this gas into the second reaction
vessel. The idea of the water bath is gentle controllable heat. Good luck and be careful and remoive any flammable liquids and easily oxidizables
before you proceed!
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KABOOOM(pyrojustforfun)
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<blockquote>quote:<hr>I was especially intrigued by use of ClO2 with hot water for HClO4<hr></blockquote>u mean making HClO4
using ClO2? sounds odd, ClO2 hasn't got enough O to be even anhydride of chloric acid. plz give more info on it.<br>ever thoght of mixing
sols of dihydrazinium sulfate and barium chlorite? if ClO2<sup>-</sup> doesn't <i>react</i> with hydrazine N2H5ClO2 will
form. a incredibly unstable and sensitive and damn powerful explosive with perfect
OB!<br>N<sub>2</sub>H<sub>5</sub>ClO<sub>2</sub> <s> ></s>
N<sub>2</sub> + 2H<sub>2</sub>O + HCl
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chloric1
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KABOOM. Yes I suppose, in theory, you could react hydrazine sulfate with barium chlorite to make hydrazine chlorite but I have never heard fo its
existence and I think any attempt at its developement would result in detonation. As for your question about perchloric acid from ClO2 it is a
complex process. Firstly ClO2 reacts with water to form chloric AND chlorous acid much like NO2 makes nitric AND nitrous acids in dilute solutions.
This is because the ClO2 oxidizes itself! How is that for oxidizing power!?? Second chloric acid solution when concentrated by boiling decomposes to
HClO4 an chlorine gas. The chlorine is a result of the reduced portion of the chloric acid. So, as you may guess, the yield is poor but if you
have large quanties of potassium or sodium chlorate, battery acid, and oxalic acid; you could make a considerable quanitity of perchloric acid.
Personally I still have about 1500ml of 70% perchloric acid but I amy perform this experiment just for academic curiosity.![:P](./images/smilies/tongue.gif)
[Edited on 10/11/2003 by chloric1]
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KABOOOM(pyrojustforfun)
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yyeeeeaah
I can finally have some perchloric acid I don't care for low yield. it's awhile i've been seeking for this baby.
is it what happens?
14ClO<sub>2</sub> + 4H<sub>2</sub>O <s> ></s> 8HClO<sub>4</sub> +
3Cl<sub>2</sub>
[Edited on 12-10-2003 by KABOOOM(pyrojustforfun)]
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blip
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This is what's really going on, if I'm not mistaken:
2ClO<sub>2</sub> + H<sub>2</sub>O <s> ></s> HClO<sub>2</sub> +
HClO<sub>3</sub>
HClO<sub>3</sub> + HClO<sub>2</sub> <s> ></s> HClO<sub>4</sub> + HOCl
4HOCl <s> ></s> HClO<sub>4</sub> + 3HCl
I don't see where chlorine gas would evolve, though.
Btw PJFF, last time I tried doing a strike through a greater-than symbol, it went through and looked quite bad. Apparently something has changed.
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chloric1
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Quote: |
I don't see where chlorine gas would evolve, though.
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Realise that in ClO2 the chlorine has an oxidation number of 4 and when this forms chlorous and chloric acids, part of the chlorines are oxiidized to
+5 while the others are reduced to +3.
Likewise, a simular thing happens when you heat chloric acid to decomposition. remember that if you melt KClO3 it autoxidizes into KClO4 and KCl now
the same is true of the free acids. Hence the evolution of chlorine gas. But, and I mean but, you will have chlorine in various concentrations in
this aqueis concoction. So it could be that the chlorine is oxized as it is evolved but I doubt it.
Fellow molecular manipulator
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blip
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Oh, like one of the oxidizing acids oxidizes HCl into Cl<sub>2</sub>? I didn't think of that, sorry.
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KABOOOM(pyrojustforfun)
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blip let's disscuss HTML tags using U2Us or make a topic on forum matters. it doesn't have any thing to do with chlorine dioxide(as far as I
know![;)](./images/smilies/wink.gif) ). I
also misunderstood u by <i>greater-than symbol</i>![;)](./images/smilies/wink.gif)
chloric1 please tell us your source(s) of info.
I think when boiling a chlorate salt adding a dilute solution of oxalic acid with very slow rate (drop by drop) you get chloride and perchlorate at
the end. if this works it'll be quite safer and easier than getting chlorats to melt.
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Marvin
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Ive heard of the oxalic method before, but I havnt heard of using dilute sulphuric acid to help push it along, interesting. Should result in a
mixture of 2 volumes CO2 to 1 volume ClO2. A lot safer and on the right side of the 300 torr pop/bang threshold.
Needs to be mentioned that this is dilute sulphuric acid, as concentrated sulphuric acid and chlorates is a very bad thing.
Hydrazine chlorite will almost certainly just evolve nitrogen gas on formation as the solutions mix.
I have a big problem with the perchloric acid idea. To start with just assuming that a solution of the gas in water will be a solution of both acids
isnt right. Like ammonia which in solution is mostly NH3 and is only a tiny part NH4OH, most of the chlorine dioxide will just be as chlorine
dioxide. Given the method of preparation I wouldnt expect the solubility in water to exceed a few grams a litre, and when you heat it, Id expect it
to leave if it can. Given you start with a solution thats only about 0.3% and you enter into a process you think will be low yeilding, I wouldnt hope
much for a result. Chloric acid itself seems to like to decompose by producing oxygen, not the disproportionation we were expecting and furthur
wrecking the yeild.
I would think that carefully fusing the pure salt could work. Or a bit safer, oxidising it to perchlorate with silver(I) catalysed persulphate in aq
solution.
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chloric1
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I think when boiling a chlorate salt adding a dilute solution of oxalic acid with very slow rate (drop by drop) you get chloride and perchlorate at
the end.
Ok I am sorry, I must have been unclear in my original message. The information is based on my experiments. As I have said I have only used test
quantities. But what I did was I took solid KClO3 and solid Oxalic acid then I added sufficient battery acid to cover witha little extra. I heated
this in a water bath to drive off chlorine dioxide. What i was suggesting was dissolving this gas into ICE cold water and then heating this slowy to
generate HClO4. But if I had not said so before I have only generated the gas and have not performed the autooxidation.
Fellow molecular manipulator
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KABOOOM(pyrojustforfun)
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Marvin did you mean ClO<sub>2</sub> is in equilibrium with the acids?
chloric1 I still don't know whether you theorised the formation of HClO4 via ClO2 or you got the info from a scientific source?
Edit: I hadn't read the <i>perchloric acid preparation</i> topic. it's been disscused there.
[Edited on 19-10-2003 by KABOOOM(pyrojustforfun)]
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chloric1
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Chlorine dioxide
Ok THe HClO4 from ClO2 and hot water is from more than 1 scientific source but it has been many years so which one I do not recall. My experiments
are merely pointed out that ClO2 from KClO3 and oxalic/sulfuric acid solution proceeded smoothly because KClO3 has limited solubility. I was just
suggesting some output uses for the gas. It is rather interesting in itself and I like the smell .
But if you Whiff it do it indirectly because it can pack a wallop and put you in the hospital!!![:o](./images/smilies/shocked.gif)
Fellow molecular manipulator
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