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careysub
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Quote: Originally posted by XeonTheMGPony  | it is all math work, here is the pdf. Rule of thumb the further you are or the more stuff to absorb the energy the better.
when pressing caps I use dry towels wrapped around the press to absorb the shock wave and to dampen any shrapnel produced, cotton is a good acoustic
absorber. |
Comment about this file - the lowest blast injury level given is
"0.35 kg/cm2. Minimal distance of possible rupture of tympanic membranes."
It is important to realize that membrane rupture is the maximally severe form of hearing injury - hearing loss injury starts at much lower pressure
levels.
Plugging 0.001 kg (one gram) and one meter into the Sadowsky formula gives an overpressure of 0.118 kg/cm2, far more than enough to break a window
(0.05 kg/cm3 given as the level for this), and certainly hazardous to hearing.
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James Ikanov
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Somewhat differing from the main topic, where would something like nitrogen-tri-iodide fall in this equation?
It's obviously never going to get to much more than a few grams (I'm bad at estimating things) but how brisant might a novelty like that be compared
to, say, flash or blackpowder? I'm under the impression the usual demonstration amounts are too small to do much and that it's a rather wimpy
explosive anyway, but I figured I'd ask since I can't find too much on its VOD or such.
“To do good work one must eat well, be well housed, have one's fling from time to time, smoke one's pipe, and drink one's coffee in peace” -
Vincent Van Gogh
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careysub
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| Quote: Originally posted by James Ikanov | Somewhat differing from the main topic, where would something like nitrogen-tri-iodide fall in this equation?
It's obviously never going to get to much more than a few grams (I'm bad at estimating things) but how brisant might a novelty like that be compared
to, say, flash or blackpowder? I'm under the impression the usual demonstration amounts are too small to do much and that it's a rather wimpy
explosive anyway, but I figured I'd ask since I can't find too much on its VOD or such. |
A few grams is excessive for a first attempt. Try 0.5 grams.
The Royal Society of Chemistry has a safe demonstration procedure:
http://www.rsc.org/Education/EiC/issues/2010May/ExhibitionCh...
A key point with this substance - after it is prepared, it is not sensitive as long as it is still wet. It must be laid out for demonstration
detonation, and decontamination at once, and never disturbed again until exploded and decontaminated.
Rewetting it to render it insensitive again is an unreliable procedure.
If we use Wikipedia's decomposition energy for complete decomposition:
2 NI3 (s) → N2 (g) + 3 I2 (g) (−290 kJ/mol)
it is about 1/6 as energetic as TNT, and one of the weakest explosives known.
[Edited on 9-9-2016 by careysub]
[Edited on 9-9-2016 by careysub]
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Bert
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Threads Merged
9-9-2016 at 13:26 |
Tricka90
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Thank you everybody for all the replys.
The formulas and documents you posted are very useful, the problem is they don't seem applicable to small quantities of primary explosives:
| Quote: |
From this it would give the safe distance of 3 meters for one gram |
I'm not expert but we all can agree for such distance to be extremely conservative (unless the explosive is confined in a material which can unleash
dangerous fragments when exploding).
| Quote: |
if you are handling EM materials for all practical purposes there is no safe distance. You are working entirely in the danger zone. Safety lies in
making sure the stuff you handle NEVER explodes. |
Well, I agree with you, but I think in some cases one can withstand a detonation without getting hurt if there's a proper gap between the explosive
and his hand. In such cases a safe minimum distance does exist and is also very important. For example when handling less than 100mg SADS in order to
manufacture a blasting cap no permanent damage to the hands would occur if a gap of a few tens of centimeters exists. Otherwise the damage could be
serious, so I say it would be reasonable to evaluate and respect a safe minimum distance in those cases. At least that's what I feel fair to say
considering my very short practical experience on the subject, so it's possible I'm wrong.
Also I can't completely rely on the fact that doing all things properly means no detonation will ever occur. I think I can't be 100% sure so I'm
always prepared for an explosion.
As for the hearing protection I think it would be very stupid to lose the hearing because of unespected detonation, considering that having ear plugs
always on is easy, cheap and doesn't hinder one's ability to handle the substance (as it does maintaining a safe distance, which is often unfeasible).
[Edited on 10-9-2016 by Tricka90]
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stoichiometric_steve
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Is there a quick way to distinguish acetic anhydride from acetic acid or from a mixture of both the anhydride and acid?
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PHILOU Zrealone
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Metallic zinc will set H2 gas free with acetic acid owing to available proton.Acetic anhydride should remain inert towards the naked metal.
For the mix maybe density or boiling point may be of some use.
PH Z (PHILOU Zrealone)
"Physic is all what never works; Chemistry is all what stinks and explodes!"-"Life that deadly disease, sexually transmitted."(W.Allen)
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Metacelsus
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Acetic acid is miscible with water. Acetic anhydride is not (but does react with it). You could add a drop of the unknown to a small amount of cold
water, and see if it's homogeneous. The zinc idea is also good, and you could probably use other metals too.
[Edited on 9-10-2016 by Metacelsus]
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Gemlingur
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RDX plasticiser
I made a small batch of RDX by the E process. Now I've been reading about the additional stuff you put in it to make it plastic, and tbh I'm not
really in the mood to get hold of all that stuff. So I was wondering, would it be possible to use something as simple as xanthan gum or dextring or
something alike?
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Bert
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Threads Merged
13-9-2016 at 04:31 |
Fulmen
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Oil or wax does the trick. Try making a dummy compound with sugar, salt or whatever inert you have that matches the particle size and see what you
think. A few (perhaps 5) percent of wax should phlegmatize the RDX, it won't be plastic but well suited for pressed charges. 10% heavy oil should
produce a putty-like plastic. Not as nice as PIB-based compounds but it will work just fine.
We're not banging rocks together here. We know how to put a man back together.
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James Ikanov
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What exactly is this "heavy oil" you refer to?
Serious question, google just gives me some real generic stuff. Is it a motor oil, some sort of specific brand or something?
“To do good work one must eat well, be well housed, have one's fling from time to time, smoke one's pipe, and drink one's coffee in peace” -
Vincent Van Gogh
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Fulmen
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Any thick oil. Motor oil works, but my favorite is chain saw lubrication. You could also try grease.
We're not banging rocks together here. We know how to put a man back together.
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Tricka90
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ETN or Picric Acid as my first secondary synthesis?
After gaining some experience with the manufacture of primaries I'm going to try and make my first secondary. I finally decided to either make ETN or
Picric Acid since I have all the ingredients available. What of them would you suggest to a beginner? ETN seems easier to make, but it's also an
extremely sensitive secondary. On the other hand Picric Acid synthesis is a bit harder and it's also toxic but his sensitivity is very low.
So what do you think is the right choice to start experimenting with secondaries?
[Edited on 13-9-2016 by Tricka90]
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NeonPulse
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Picric acid is definitely harder and will make dangerous fumes. It is also a hot nitration and gas several steps. Not really a beginners synthesis. I
would do ETN or even Nitrocellulose first to get a feel do how a nitration goes. My two cents.
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careysub
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| Quote: Originally posted by NeonPulse | | Picric acid is definitely harder and will make dangerous fumes. It is also a hot nitration and gas several steps. Not really a beginners synthesis. I
would do ETN or even Nitrocellulose first to get a feel do how a nitration goes. My two cents. |
I found the Bodine procedure for picric acid straightforward and reliable - did it outside and was careful about the fumes. (I just wanted a little
for an amine isolation reagent.)
[Edited on 14-9-2016 by careysub]
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Zephyr
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| Quote: Originally posted by careysub | | Quote: Originally posted by NeonPulse | | Picric acid is definitely harder and will make dangerous fumes. It is also a hot nitration and gas several steps. Not really a beginners synthesis. I
would do ETN or even Nitrocellulose first to get a feel do how a nitration goes. My two cents. |
I found the Bodine procedure for picric acid straightforward and reliable - did it outside and was careful about the fumes. (I just wanted a little
for an amine isolation reagent.)
[Edited on 14-9-2016 by careysub] |
Nice! I did it recently also. So far I've been storing it dry in a glass jar with a plastic cap, how do you all store your's? Is the water necessary?
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Gemlingur
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| Quote: Originally posted by Gemlingur | | I made a small batch of RDX by the E process. Now I've been reading about the additional stuff you put in it to make it plastic, and tbh I'm not
really in the mood to get hold of all that stuff. So I was wondering, would it be possible to use something as simple as xanthan gum or dextring or
something alike? |
Tested it out with salt instead of RDX, about a seventh of total volume was xanthan, it started out as a very moldable kind of a thick, fibrous ice
cream, but when left to dry it started depositing either xanthan or salt at the edges, and wouldn't join itself when folded. Next test will be with
varying amounts of xanthan, and then some petroleum jelly to see how that changes things. Making xanthan gum first and then trying to knead the salt
in proved unsuccessful.
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Laboratory of Liptakov
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When you're will be in the mood, go to the electro store and buy self-vulcanizing tape. All those things are 3: gasoline, oil and tape.
https://www.youtube.com/watch?v=CBK-NR4suEE
This tape = end of worry with plastification anything.
http://www.ebay.com.au/itm/SCAPA-2501-Quality-Self-Amalgamat...
Dr...
Development of primarily - secondary substances CHP (2015) Lithex (2022) Brightelite (2023) Nitrocelite and KC primer (2024)
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Maker
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Is there any way of quantifying the 'strength' of a solvent? And if so, what are some of the strongest?
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Bert
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| Quote: Originally posted by Maker | | Is there any way of quantifying the 'strength' of a solvent? And if so, what are some of the strongest? |
You would need to be more specific as to your material of interest. What do you want to dissolve? And why?
Rapopart’s Rules for critical commentary:
1. Attempt to re-express your target’s position so clearly, vividly and fairly that your target says: “Thanks, I wish I’d thought of putting it
that way.”
2. List any points of agreement (especially if they are not matters of general or widespread agreement).
3. Mention anything you have learned from your target.
4. Only then are you permitted to say so much as a word of rebuttal or criticism.
Anatol Rapoport was a Russian-born American mathematical psychologist (1911-2007).
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Maker
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| Quote: Originally posted by Bert | | Quote: Originally posted by Maker | | Is there any way of quantifying the 'strength' of a solvent? And if so, what are some of the strongest? |
You would need to be more specific as to your material of interest. What do you want to dissolve? And why? |
I didn't have a specific material in mind, just a general wondering.
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kratomiter
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| Quote: Originally posted by Tricka90 | After gaining some experience with the manufacture of primaries I'm going to try and make my first secondary. I finally decided to either make ETN or
Picric Acid since I have all the ingredients available. What of them would you suggest to a beginner? ETN seems easier to make, but it's also an
extremely sensitive secondary. On the other hand Picric Acid synthesis is a bit harder and it's also toxic but his sensitivity is very low.
So what do you think is the right choice to start experimenting with secondaries?
[Edited on 13-9-2016 by Tricka90] |
I don't find the synthesis of Picric Acid from ASA that difficult, but if you don't wanna deal with high temperatures and still want to make a
nitrophenol, try with trinitrophloroglucinol if phloroglucinol is available for you. Synthesis is perfomed at 0ºC and yields are good (look at
Studies on 2,4,6-trinitrophloroglucinol (TNPG)⎯A novel flash sensitizer).
[Edited on 15-9-2016 by kratomiter]
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NeonPulse
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I would say also the synthesis of TNP is not really that hard, but for experienced people. It's not really a beginners one and although Rosco bodine's
picric acid procedure is detailed enough so even a layman can get it, if you have zero experience with synthesis of energetics I wouldn't do this as
the first one. ETN is easier to make and more powerful it is also less dangerous with only nitric vapour to worry about rather than copious amounts
of potentially deadly fumes and hot acid.
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Bert
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ETN first, IMHO. I did personally make trinitrophenol before ETN, as Axt on the old E&W forum had not yet directed the amateur chemistry
community towards the newly available erythritol feed stock & original patent information when I first got the interest to perform such
operatuons- also nitroglycerin and nitrocellulose as a highschool kid, long before the advent of "windows" and the general public venturing out onto
the WWW.
Rapopart’s Rules for critical commentary:
1. Attempt to re-express your target’s position so clearly, vividly and fairly that your target says: “Thanks, I wish I’d thought of putting it
that way.”
2. List any points of agreement (especially if they are not matters of general or widespread agreement).
3. Mention anything you have learned from your target.
4. Only then are you permitted to say so much as a word of rebuttal or criticism.
Anatol Rapoport was a Russian-born American mathematical psychologist (1911-2007).
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Bert
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Somewhere in the energetic materials forum, there is attached to a post a blasting cap diagram (patent drawing?) that details a cap with a small,
pyrotechnicaly driven flyer with electric ignition which strikes a secondary explosive, rather than using a HV discharge or a standard primary. As far
as I can recall, the propellant for the flyer was nitrocellulose-
I had downloaded this to my old iphone, but do not seem to have saved it to my desktop- and that phone is now dead.
Ring a bell with anyone?
Related question- What is the highest "flyer" velocity that you know of anyone achieving with a deflagreting solid propellant system, rather than
driven by a detonation. Ideally without needing something, (expensive, non disposable!) like a taper bore, or other complex, heavy metal fabrication?
[Edited on 21-9-2016 by Bert]
Rapopart’s Rules for critical commentary:
1. Attempt to re-express your target’s position so clearly, vividly and fairly that your target says: “Thanks, I wish I’d thought of putting it
that way.”
2. List any points of agreement (especially if they are not matters of general or widespread agreement).
3. Mention anything you have learned from your target.
4. Only then are you permitted to say so much as a word of rebuttal or criticism.
Anatol Rapoport was a Russian-born American mathematical psychologist (1911-2007).
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James Ikanov
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This sounds a bit like a poor man's slapper detonator?
I haven't seen that specific setup....
When you say "non-detonating propellant" do you mean just the igniter or the entire assembly?? I assume the first....
If I was up for making speculation I have a relatively unused (and untested) mixture that might be very good for launching a flyer pretty
effectively...... but I don't know of anything tested.
Honestly I see no reason why you couldn't just start with a slightly scaled up blasting cap assembly and a metal plug? Eg, a small amount of loose
secondary at the bottom (possibly with a sensitizer), a ball bearing (of as close as possible to internal diameter of the tube), some NC or flash,
then your initiator (fuse or wires) then crimp it? But that's rather vague....
Apologies if I seem rather useless.
“To do good work one must eat well, be well housed, have one's fling from time to time, smoke one's pipe, and drink one's coffee in peace” -
Vincent Van Gogh
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