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The_Davster
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[*] posted on 21-5-2006 at 14:32
Liquification of oxygen




Oxygen was generated in the 100mL 3 neck flask by addition of diluted 35% peroxide(to around 10-15%) to MnO2. The oxygen was ran through a wash bottle full of CaCl2, I did not feel like packing a tube. The oxygen was then ran through a dewar condensor filled with LN2. I collected around 5mL of liquid oxygen.

However, the water in the oxygen generator began to boil, and the 24/40 stopper blew out, so I removed the water in there, closed it up and let fresh peroxide drip in. While switching it the liquid oxygen I had collected evaporated. I stepped up the peroxide addition to make up my losses, and was getting an almost steady flow of liquid oxygen out of the condensor, but I was not paying attention to the liquid level in the 100mL flask. It filled and liquid went up the side tube of the addition funnel, dripped into the fresh peroxide, and blew off every stopper there. oops. By the time I fixed it the liquid oxygen had evaporated.

In conclusion: I need a bigger gas generating flask, but seeing as I had a difficult time cleaning the glass after the MnO2 in there, I will just get a cylinder of oxygen soon and try this again. Collecting the liquid oxygen in a small dewar would also be a good idea. I will see if I could borrow one from someone I know.

EDIT: Yes I know my lab is a mess...

[Edited on 21-5-2006 by rogue chemist]




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[*] posted on 21-5-2006 at 14:53


Now that is cool.

My lab's a mess too.
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[*] posted on 22-5-2006 at 07:31


Cool! I liquified O2 once as well. I filled a dewar with liquid N2, coiled up a piece of metal tubing, submerged the tubing in the liquid N2, and ran O2 from a cutting torch tank through it. I collected the pale blue liquid O2 in a beaker.

One of my friends was messing around with some burning paraffin wax in a coffee can, and we got the bright idea to pour some O2 onto it. We taped a styrofoam cup onto the end of a 20 foot long stick, put ~50-100 ml O2 (liq.) into it, then carefully poured it over the burning paraffin wax. We were expecting a big fireball, but what we got was an intense, loud, explosion! It sounded like a bomb went off!:o Of course we ran inside and turned off all of the lights after making sure nothing was going to burn down.

And of course, that was a long time ago; I'm much more mature these days! Well....
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[*] posted on 22-5-2006 at 07:45


Why not just use dried air? Argon, CO2, and O2 should condense. The cold N2 could be used to precool the dried air.
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[*] posted on 22-5-2006 at 14:35


You don't need to build any apparatus if you want LOX.

Get some tinfoil (normal household Al foil) and fold it into a conical shape, with a closed tip on the bottom.
Suspend it from a stative with strings.
Test for leaks: fill it with water. No water must drip out anywhere.

Dry it, and fill the thing with liquid nitrogen.
LOX will condense on the outside from the air and drip down at an amazing rate, way faster than if a metal container is used, due to the extremely efficient heat transfer through the thin Al foil.
Collect the LOX in a test tube cooled from the outside with LN2.
You will see its blue color, and if you drip some on burning wood or paper, huge eruptions of flames will be produced.
A cigarette soaked in LOX will burn fiercely and be consumed in a matter of seconds.

Frost will collect on the outside of the thing after short time and act as an insulator, slowing down LOX condensation.
Just empty the thing, and dry the outside with a heat gun.

The LOX produced this way is of course not very pure, it should better be called "oxygen enriched liquid air".
However, the oxygen content is high enough to allow the blue color to be seen (liquid air is nearly colorless).
The oxygen content can be increased by allowing a portion of the liquid to evaporate by removing the LN2 cooling on the outside of the test tube.




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[*] posted on 2-6-2006 at 06:19


Where did you get liquid nitrogen?
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[*] posted on 2-6-2006 at 10:38


You can get it at any major gas supplier (i.e. praxair, air liquide, linde, matheson trigas etc.). Prices around here are about 60-70 cents a liter, and sometimes the guys will fill up a 35L dewar for free.
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[*] posted on 2-6-2006 at 14:13


After reading this last response I called up my local gas supplier. I told him I had a 1-liter dewar. He said he could fill this with LN2 at any time. I had no idea it was this easy.

This seems like it would be a colder, cleaner, and cheaper method of obtaining a cryogenic bath than using an acetone/dry ice mix. Is this true?




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[*] posted on 2-6-2006 at 14:54


I was once in need of a cold bath for condensing an amine gas. I usually used dry ice/acetone but was out of dry ice, so I used liquid N2 instead. It worked well, but perhaps a little too well; the amine froze and plugged up the tube entering the condensation flask. Then the increased pressure on the generation system caused stoppers to pop out and other unpleasantness!

It's certainly colder. Maybe cleaner, but I don't really think of dry ice/acetone as all that messy. I don't know if it's cheaper or not, I never payed attention to cost.
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[*] posted on 2-6-2006 at 15:09


LN2 is much easier and especially cheaper for me to obtain (although it still costs 2,60€ per Liter) than dry ice, the supplier is only ten minutes away. They even let you borrow a 10L dewar for free.

However, the disadvantage is that you can't liquefy ammonia as nicely as you can with dry ice. It's way too cold for some applications.
It might be an idea to stir LN2 into acetone to cool it down to the required temperature, so that the ammonia doesn't freeze like it will do with plain LN2. You could even make "icecubes" out of solid acetone, and put these into liquid, precooled acetone to increase the cooling capacity of the cold bath.




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[*] posted on 29-5-2007 at 16:55


this is fricken awsome!!!!!!!!!!!!!!
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[*] posted on 29-5-2007 at 19:32


Quote:
Originally posted by garage chemist
A cigarette soaked in LOX will burn fiercely and be consumed in a matter of seconds.


... or it might explode outright ....
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[*] posted on 29-5-2007 at 22:18


What I have always wondered is how hard it would be to build a DIY refrigeration system to generate LOX. Something like this.


[Edited on 29-5-2007 by alancj]

Temp High and Low p39.jpg - 57kB
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[*] posted on 31-5-2007 at 15:23


Ok, i am over my previous excesive excitment as with my last post.

I called all the gas suppliers in the phone book. All except for one said no way. The one person who said it would be possible for an individual to purchase said I would need a dewar flask. The cheepest one: 595 USD!!!!!I asked him about thermos bottles and he was steadfast that they would not work. It seems to be the only gas supplier around. Any ideas?

Thanks
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[*] posted on 31-5-2007 at 15:35


you can find cheaper one on eBay or labX, or check that website for new smaller one: http://www.cryodewars.com/index.php?cPath=1_2



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[*] posted on 1-6-2007 at 02:09


<<< The cheepest one: 595 USD!!!! >>>

That's b/c you need a pretty big one.

use of a thermos bottle will not git yer L2 home B4 it evaporates............




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[*] posted on 1-6-2007 at 06:23


Its not true, a thermos bottle will hold LN2 quite well. Of course not as long as a dewar, but at least 24 hours for a two liter thermos.
A thermos would be useable for carrying LN2 home and using it immediately.
Remember to drill a small hole into the stopper.

Dont buy new dewar flasks, they all cost a fortune as you have seen.
Look on ebay for used ones.




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[*] posted on 1-6-2007 at 06:27


Would it be worth it to make a dewar vessle yourself? It would require glass bottles which could be silvered using tollens reagent and glucose, styrofoam could provide a lot of additional insulation, the hardest part would probalby be find bottles that fit into eachother. Perhaps using tall beakers might work of you make a stopper of really thick (silvered?) styrofoam. Polyurethane foam might be evan more usefull in this case you could just spray it between the two bottles.



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[*] posted on 1-6-2007 at 12:09


The trouble with making a dewar oneself are twofold:

Insulation quality:

LN2 has a fairly low specific heat capacity. The insulation does not have to be that far off perfect to sustain quite rapid boil-off.

Materials:

LN2 has a boiling point below that of oxygen. Thus if a porous foam is used as insulation, LOX condenses and bad things happen. Quite a few materials are shock sensitive when soaked in LOX.

Yet another problem is that common polymers tend to be quite fragile at low temps.

Saying that though. It certainly is possible to store LN2 for short periods of time in a vessel insulated with a suitable closed cell foam. You might even be able to purchase these relativly cheaply, as these things quite often turn up in undergrad. physics labs to store LN2 for a few hours.
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[*] posted on 1-6-2007 at 14:35


I recall seeing perlite is suitable for a suprising insulation capacity. Vermiculite may also be good.

Tim




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[*] posted on 1-6-2007 at 15:02


Using foam as the primary insulation has one other potential problem. Consider what is making the voids in the foam - what gas is filling the cells? Simply cooling the foam down a lot is going to reduce the pressure in the cells, if they get cold enough the gas will condense to a liquid. Foaming agents that I know of are low boiling alkanes, fluorocarbons, and CO2.

An outer wrapper of foam can help cut down boil-off a bit, and provides mechanical protection.
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[*] posted on 3-12-2007 at 21:17


I think it would be nice, if you were too poor to buy your own DEWAR, to design a fake one so your supplier wouldn't know it wasn't actually a DEWAR. Surely it wouldn't be too hard to make something LOOK like a DEWAR.

I wouldn't recommend it. Just speculation.




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