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markx
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Quote: Originally posted by PHILOU Zrealone  |
Sand will dry faster in a kind of tumble drier or into a fluidized bed (warm air from under through the sand that is lifted up (fluidized) a little
and fall back down). |
As I found out, much to my surprise, a heating cabinet and spreading out a thin layer of the stuff also does wonders 
And yes....IT WERKS!!!
So I prepared a set of samples:
![WP_20170201_001[1].jpg - 1.1MB](https://www.sciencemadness.org/whisper/files.php?pid=473362&aid=56616)
2* 50mg 100% SADS for baseline
1* 50mg 15% KClO3
1* 50mg 20% KClO3
1* 50mg 30% KCO3
2* 100mg 100% SADS for comparison
The cell was loaded with 40g of evaluation sand 250/100um fraction for all tests and then sieve analysis was performed with RETSCH AS200 apparatus on
100um sieve to get the fraction that passes the 100um limit as the assessment for brisance.
The first results were as follows:
Baseline <100um for 50mg SADS 100% : 3,89g
Baseline <100um for 100mg SADS 100% : 5,82g
15% KClO3 <100mg fo 50mg : 4,42g
20% KClO3 <100mg fo 50mg : 4,09g ?? (probably an error in assessment)
30% KClO3 <100mg fo 50mg : 4,45g
This proves, although inconclusively, my previous assessment of the brisanse of these mixes based on the "match shattering" method. Seems that
addition of KClO3 increases the power by quite a considerable amount compared to pure double salt.
As we can see from the baseline measurements ,the double charge of pure SADS caused about 49.6% increase in amount of <100um fraction. Where as the
addition of 15% KClO3 caused about 13,6% increase in amount of <100um fraction. Derived from that, one could quite loosely estimate that the 15%
KClO3 mix is about 27% more brisant than pure double salt. This applies only to this test under these particular circumstances and postulating that
brisance increases linearily in relation to the amount of sand crushed. Which of course is not correct, but let's just assume for the sake of
simplicity and just to make an example. All in all I'm very pleased with the performance of the cell and the first results. For further steps I will
work with 100mg samples for better resolution and make more repetitions on all datapoints to get a more conclusive result and catch the most potent
sweet point for the mix.
Oh yeah...I tried to set off the SADS KClO3 mix with friction and impact...no go, luckily it seems to be not too much more sensitive compared to pure
double salt, but extreme caution is a must.
Nice side effect which can be seen in the last picture is that the top of the sample holder is covered in a shiny well adhered layer of metallic
silver. It was deposited by the 100mg pure SADS baseline measurements. The 15% mix actually deposited a golden layer which looked even more pretty
As far as downsides of this perticular setup are concerned, then the fuse for initiation is best replaced by an electrical triggering system. The
pyrotechnical route is messy, leaves ash and stinky byproducts if a BP fuse is used and must be set off outside....but it is simple and reliable.
[Edited on 1-2-2017 by markx]
Exact science is a figment of imagination.......
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NitratedKittens
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Teeheehee, welding asses
Basket of kittens for you ........BOOM
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nitro-genes
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Great job and good lathe skills as wel! This would be a great tool to test
small amounts of pirmary explosives for their brisance with the added benfit that it includes reasonably reinforced conditions, so also usable for
less "hot" primaries so to say. As you said, one of the things that would be interesting to do is take several repetitions of exactly the same setup
to get an idea of the variation inherent to the test. Assuming you want to be able to discern a specific effect size you can calculate how many
repetitions would be needed to reach statistical significance, by the looks of it 4-5 may be enough for 10% difference.
Also, how does the packing densitty of the sand affect the test? Can imagine this depends on kernel shape and batch wise, maybe include a negative
control (just unblasted sand) as well.
Did you design the setup after a commonly used one btw? If it does, would be interesting to compare your own data with those from literature. Very
cool!
[Edited on 1-2-2017 by nitro-genes]
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MineMan
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Your results matched mine. I have found the addition of 20% Kclo3 to be best for both ignitability and brisance. This is important, as not only are
we increasing the power, we are diluting it with a cheaper chemical. Above 20% it has trouble detonating in the open when exposed quickly to a flame.
I have found also that it does not increase the sensitivity. SADS is really the most insensitive primary I think...
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markx
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| Quote: Originally posted by nitro-genes | Great job and good lathe skills as wel! This would be a great tool to test
small amounts of pirmary explosives for their brisance with the added benfit that it includes reasonably reinforced conditions, so also usable for
less "hot" primaries so to say. As you said, one of the things that would be interesting to do is take several repetitions of exactly the same setup
to get an idea of the variation inherent to the test. Assuming you want to be able to discern a specific effect size you can calculate how many
repetitions would be needed to reach statistical significance, by the looks of it 4-5 may be enough for 10% difference.
Also, how does the packing densitty of the sand affect the test? Can imagine this depends on kernel shape and batch wise, maybe include a negative
control (just unblasted sand) as well.
Did you design the setup after a commonly used one btw? If it does, would be interesting to compare your own data with those from literature. Very
cool!
[Edited on 1-2-2017 by nitro-genes] |
This testing device has not been benchmarked, at least not intentionally, against any particular device design of same function that is already out
there and being used. So comparing results number by number is probably not going to be a trivial task, but that was not my intention to begin with.
Rather I would depoly it in service of establishing a better understanding of the tendencies and relationships of the parameter known as "brisance"
with regard to composition of energetic mix or substance. These tendencies have reasonably little regard towards the particularities of the testing
device (which only sets the background system so to speak), so as long as a comparative set is tested within the same device, a comparable tendency
should reveal itself.
The parameters of sand will most definately have a major effect on the outcome of the result, as the hardness, geometry, size, granulometry and
packing density all affect the way in which energy is absorbed by the medium. I used soft limestone type to better capture the relatively small
variations in brisance and prepared the sand fraction beforehand by carefully sieving and washing out everything above 250 microns and below 100
microns grain size. The unblasted sand shows close to 100% retention on 100 micron sieve....so anything passing through after test is the effect of
the released energy. The sand surrounding the sample was not intentionally compacted (which would certainly increase the effect of crushing), but
rather just poured over it and left as is. Either way will work and reveal the same tendencies as long as one keeps it consistent through the
individual tests. So operator's adherence to preparative procedure and unbiased action is required...but that goes for all experiments
Exact science is a figment of imagination.......
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markx
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| Quote: Originally posted by MineMan | Your results matched mine. I have found the addition of 20% Kclo3 to be best for both ignitability and brisance. This is important, as not only are
we increasing the power, we are diluting it with a cheaper chemical. Above 20% it has trouble detonating in the open when exposed quickly to a flame.
I have found also that it does not increase the sensitivity. SADS is really the most insensitive primary I think... |
I did not find a decreased sensitivity towards flame initiation even up to 50% dilution in my tests....the mixes seemed to remain ever so sensitive to
the slightest touch of a flame, but brisance decreased noticeably at higher dilution ratios.
Mechanical sensitivity wise I will remain very inconclusive so far, as I have not performed any quantitative tests for the mixes. It seems to be
unaffected in direction of increased sensitivity, but for now it is best to assume the worst just in case.
Exact science is a figment of imagination.......
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nitro-genes
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Nice.. could think of some comparitative test for some diazophenols. Would
still be interesting to extrapolate results from taking some measurements from known primaries of course. Just hypothetically speaking (not really
sure what this extra data would tell you), measuring the weight of several size fractions might also be interesting, starting with the smallest
particle sizes and up, then looking at the distribution, maybe some correlations between total energy release and brisance would be apparent.
Regarding sand loading and packing by pouring, wouldn't round grains be optimal regarding density and consistency? Sharply edged sand grains take
quite some tapping to get optimal packing probably. Maybe the total weight of the sand poured in can provide an idea of the most consistent loading
procedure.
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markx
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| Quote: Originally posted by nitro-genes | Nice.. could think of some comparitative test for some diazophenols. Would
still be interesting to extrapolate results from taking some measurements from known primaries of course. Just hypothetically speaking (not really
sure what this extra data would tell you), measuring the weight of several size fractions might also be interesting, starting with the smallest
particle sizes and up, then looking at the distribution, maybe some correlations between total energy release and brisance would be apparent.
Regarding sand loading and packing by pouring, wouldn't round grains be optimal regarding density and consistency? Sharply edged sand grains take
quite some tapping to get optimal packing probably. Maybe the total weight of the sand poured in can provide an idea of the most consistent loading
procedure. |
Well yes...probably a synthetic media with closely controlled grain geometry, size and hardness would yield the most unbiased results, but I have to
work with the tools that I have at hand right now
Performing fractional sieve analysis of the crushed portion of sand is no problem from technical point of view, but I'm not really sure how to model
and interpret this data. I guess one could find out some things about the energetic as well as about the sand medium itself from these sieve curves.
This seems like a really vast field of research on its own and a rather complicated one too....
Exact science is a figment of imagination.......
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PHILOU Zrealone
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Very nice and exciting!
Your device seems to work fine (with the non negligible help of the professional "sieve analysis RETSCH AS200 apparatus").
No real need to compare vs other devices as long as you keep your results and methodology coherent with itself and use one ore more
standards...Pb(N3)3, AgN3, Hg(ONC)2, AgONC, Pb(picrate)2, DDNP...
Then any amateur building such a device can correlate with its own results...by using same standards...and finding its own specific geometric factor.
Ws(g) = G*Ei*WEi(g)*f
where
Ws(g) = weight of sand crushed
G = geometic factor
Ei = explosive factor (specific to each explosive; here explosive i)
WEi = weight of the given explosive i
f = function of weight (linear, quadratic or exponential)
You can also make:
-weight power curves (must be quadratic or exponential (or maybe linear) depending onto the substance) by plotting weight of primary vs sand crushed
to a finer fraction.
-volumic power curves (take into account the density variation between primaries)
-find the minimum amount of primary to effect detonation of a 50mg secondary charge (TNT, picric, RDX) ... characterized by a jump into the quantity
of sand crushed.
--> And really compare primaries or explosive power between each other or with itself in various quantities.
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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markx
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Yes, there are endless options for research here and all of them are exciting to pursue, but I guess for starters I will probe the topic of SADS/KClO3
mixes in more depth Find out the effective limits for this particular mix from
one end of dilution ratios to the other and seek out the most potent combination.
For next step I will investigate the properties of pure double salt with regard to synthesis temperature ranging from lets say 20C up to 90C with 10C
steps and see what kind of plot reveals itself. From previous experience I can say with relative confidence that the sweet spot is near 65C, but it
would be really great to see this result develop through the experimental data from brisance assessment. Perhaps there are several good spots in the
temperature range or some other details reveal themselves....
I would also like to construct a compact impact sensitivity tester to be able to check for how near the the abyss I am playing. I do have a drop
hammer device and it works like a charm, but it is bulky, noisy and uncomfortable to transport. Something spring operated with a relative scale of
potential energy should do the trick...much like a gunlock in principle. Again this would be a DIY device without a benchmark and thus lacking the
option for direct comparison of literature data. Even better if I could also come up with a compact design for friction sensitivity testing device.
The combined results from these could really lay a solid foundation for any claims on the topic. But let's see...time will tell
Exact science is a figment of imagination.......
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Laboratory of Liptakov
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SADS
SADS belongs nowadays between a best primary. Not poisoned, with relatively available precursors. Therefore is this research pretty interesting,
because price silver is high always. Adding 20% KClO3 is price of course lower and power this mixture is even higher. Next questions is sensitivity
this mixture and stability after for example half of year. I Estimate, that some EM can be initiated directly with this mixture, without secondary
EM. Or secondary EM will require lower amount this mixture for full drive. Which is advantage again. Very interesting the research.
........LL.......
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markx
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| Quote: Originally posted by Laboratory of Liptakov | SADS belongs nowadays between a best primary. Not poisoned, with relatively available precursors. Therefore is this research pretty interesting,
because price silver is high always. Adding 20% KClO3 is price of course lower and power this mixture is even higher. Next questions is sensitivity
this mixture and stability after for example half of year. I Estimate, that some EM can be initiated directly with this mixture, without secondary
EM. Or secondary EM will require lower amount this mixture for full drive. Which is advantage again. Very interesting the research.
........LL....... |
I do concur to the opinion that SADS can be considered as one of the most reasonable choices of primaries in the amateur practice realm. When prepared
under optimal conditions (elevated synthesis temperature and strongly acidic environment), it displays inherently passive behavoiur against
impact...at least on par with heterocyclic nitramine secondaries. My drop test device was unable to initiate it at the maximum height of about 70 plus
cenitmeters with a 2kg impact weight. In comparison an early sample that was prepared at room temperature in acidic environment was highly impact
sensitive and could be set off with a slight tap of an hammer. The devil lives in details and so far friction and electrostatic branches are
unexplored from my side...a serious shortcoming that I have to rectify.
As for the cost of materials viewed from the amateur practice side are quite negligible, so the dilution with chlorates mostly just serves to satisfy
the scientific couriosity
Nevertheless an in depth investigation might unveil some details that might make it sustainable for industry practice in some "niche" applications,
but given the high content of a precious metal and the cost involved makes the chances quite slim.
Exact science is a figment of imagination.......
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markx
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A slight update on generic developments regarding evaluation mediums seen below:
![WP_20170203_001[1].jpg - 1.3MB](https://www.sciencemadness.org/whisper/files.php?pid=473564&aid=56652)
The left one is quartz sand fraction and the right side one is limestone sand. Both have reasonably same granulometry and have been washed, sieved and
dried meticulosly to rid it of any <100um fines. Totally different animals though....and not just because of the coloration
As I suspected before, the quartz sand is too hard for testing of SADS and shows close to zero crushing effect after 50mg and 100mg samples being
fired. So it can not be used to test this substance for brisance.....which is actually great, because it opens up a way of cancelling out the effect
of the primary initiator stage when testing for secondaries and hence yields a very precise and unbiased result that is purely due to the secondary
stage firing up. A very exciting discovery
On a more sad note I have run out of limestone sand fraction and can not continue to test for the series today. I managed to get enough sand for two
test shots of 30% KClO3 dilution mix and surprisingly the results are quite exactly on par with the 20% dilution results. Both hover about 25-27%
above baseline brisance. Quite neat if one third of the costly ingredient can be replaced with a virtually free component and still get a massive gain
in output
I will have to hog a massive sample from next shipment of limestone filler and prepare a sizeable stock of testing media. Then a full run of
repetitions can be made in one go and the results lined up on a nice graph.....can't wait to get working on it
[Edited on 3-2-2017 by markx]
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Laboratory of Liptakov
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SADS
Once again, I would sum up the principles for the preparation yield 450 mg SADS:
1) Solution, maximum pure all reagents: 8,7g H2O + 1,82g HNO3 65% + 700 mg AgNO3 in high cylinder glass is dissolved. Temperature go to on 65 - 70C
- hold.
2) Generator acetylene : 40g pure H2O + 1,5g pure CaC2, start temperature 20 C.
3) tube (plast) for bubble with cigaret filter (or 2 filter series ?)
4) Start generator, waiting 30 second before insert pipe to solution 65 C.
5) cylinder glass cover against light
6) Bubble 4 minute, pipe out.
7) Separation on inert Buchners vacuum aparatus (cover light)
7.1) Separation on wet pure filter paper, from distilled washing (cover light )
8) Drying on this filter paper, thin layer 1 mm, dry air 25 C, (cover light)
9) waiting 12 hours on total dry EM, closing in plast container, cover light.
If is someplace error, please repair instantly from your experiences. Thanks..............LL
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Laboratory of Liptakov
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SADS
Still more question: Should be possible counting, how much pure Ag is added to 65 % HNO3 for preparation solution, which will directly used for
prepare SADS. Without process separation, drying a weighing silver nitrate and after again dissolving in 28% solution HNO3. Thus so, that solution
will content 28% concentration of HNO3 + silver nitrate before start of bubble gas C2H2. For example, in 10g HNO3 65% dissolved 500 mg Ag. And bubbe.
Because any preparation and manipulation with silver nitrate Introduces impurities into the process. When we have only acid and Ag powder. Which is
usual.........LL
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markx
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| Quote: Originally posted by Laboratory of Liptakov | | Still more question: Should be possible counting, how much pure Ag is added to 65 % HNO3 for preparation solution, which will directly used for
prepare SADS. Without process separation, drying a weighing silver nitrate and after again dissolving in 28% solution HNO3. Thus so, that solution
will content 28% concentration of HNO3 + silver nitrate before start of bubble gas C2H2. For example, in 10g HNO3 65% dissolved 500 mg Ag. And bubbe.
Because any preparation and manipulation with silver nitrate Introduces impurities into the process. When we have only acid and Ag powder. Which is
usual.........LL |
I use 4g metallic silver in 20ml 65% HNO3 which is diluted with 20ml of distilled H2O to speed up the reaction (silver does not dissolve in
concentrated nitric acid too eagerly). After that another 20ml of water is added and temperature brought up and stabilised at 65C. Then bubble C2H2
for 10minutes under vigorous magnetic stirring and filter....wash filtrate with distilled water several times...rinse...store damp on the very same
filter paper in a plastic trip baggy or let it dry in warm dark place. Very easy ratios to remember : 4/20/20/20/10
Might not be the most optimized numbers, but simple and fully functional.
Exact science is a figment of imagination.......
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Laboratory of Liptakov
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SADS
Well..! This is flash and quality answer...Thanks, all main was say. The die is cast. . .............LL
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markx
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Perhaps an illustrated synthesis run starting from metallic silver is also of value:
So let's weigh out a sample of Ag
And prepare the reactor with 20ml of water as the heel and apply PID heating on magnetic stirring
Warming up to setpoint....
Let's measure out 20ml of 65% HNO3
Dissolve the silver and filter the solution into a syringe to remove any persistent colloidal leftovers (with the help of a cigarette filter )
As one can see the solution has a characteristic blue coloration hinting to a copper contaminant in the metallic raw material....but no worries, as it
turns out, most of this impurity shall remain in solution after the reaction and can be removed with washing and filltering of final product.
Let's inject all of the silver nitrate solution into the reactor and let it equilibritate to 65C according to the inner mercury termometer. This
requires to overdrive the pid setpoint slightly.
The solution is ever so slightly murky....most likely the water contains some impurities that cause the silver to percipitate in various forms of
insoluble salts...a minor inconvenience.
Let's get some calcium carbide ready to feed into the gas generator.....a horrible low tech garde....dirty as sin in the dark night of Instanbul
Let's fill some into the gas generator that has an ice cold ice/water filling and start the 10 minute bubbling of acetylene into the reactor under
vigorous magnetic stirring....omit all filtering of acetylene gas!
Immediately a beautiful snow white double salt precipitate will begin to form...
After the ten minutes are up, the administration of gas is stopped and mixing is shut off, the product layer is thick and voluminous, filling
practically all of the liquid phase. As can be noticed, the solution above the solid still retains the characteristic blue hint of a copper impurity.
Seems that it mostly stays in solution and poses no hazard to contaminating the final product.
Spit, stir, filter, wash, squeeze, set a portion to dry.....and commence testing
[Edited on 7-2-2017 by markx]
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Laboratory of Liptakov
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SADS
Huhaha..!......white as the snow.. And in solution is absolute minimal blue. I mean, that nothing problem with copper. Nice preparation. I see pretty
sofistick aparatus for heating during a stirring. Ice water for generator ? It is better for purity C2H2 ? Or only start of gas is slowly. Because
during generate has water self heating. ..LL..
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Laboratory of Liptakov
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Look everybody on the shit on wikipedia.......
[Edited on 6-2-2017 by Laboratory of Liptakov]
[Edited on 6-2-2017 by Laboratory of Liptakov]
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markx
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Synthesis temperature, at least in my experience is of the utmost importance in this reaction....hence the PID temp control and secondary mercury
thermometer in the reactor to be double dead sure about the reaction medium's actual correspondence to setpoint.
Gas generator's icy guts only serve to control the rate of reaction and to extend a more stable output of acetylene over a prolonged period of
time.....it works pretty good.
Aa for the purity of acetylene gas and the copper contamination....it seems not to have a profound effect upon the end result.
Exact science is a figment of imagination.......
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MineMan
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Markx is dead on from my experience. I award you with the SADS certificate of the year!!
Great job. This explosive really has a future, even in industry, I think. This is one of those areas where amateurs can make great contributions.
Perhaps coating it with nanosilver would decrease static sensitivity (faraday's cage, if all silver particles are touching and coat all of the
particles)
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PHILOU Zrealone
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Maybe that the tiny copper amount helps to get a super white product...this is observed when making mercury fulminate...usually gray because of
metallic Hg...but white like snow when into the proces some Cu(2+) is present...
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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markx
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| Quote: Originally posted by PHILOU Zrealone | | Maybe that the tiny copper amount helps to get a super white product...this is observed when making mercury fulminate...usually gray because of
metallic Hg...but white like snow when into the proces some Cu(2+) is present... |
I was contemplating along the same lines....but currently have no other source of silver available to compare the results. Although when running the
synthesis at close to room temperature I have obtained a dark grey, highly sensitive product from the same silver source....still can't rule out the
involvement of copper in the process.
Exact science is a figment of imagination.......
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markx
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Whilst I am waiting for my limestone sand sample to arrive with the next shipment, I went forth and begun with the creation of a primordial secondary
test cell....the "STAMMZELLE"
Round, face off and clean the main cell chamber.....
  
Fabricate the cell bottom and sample holder....
  
And the cell support stand is completed in another session of machining....fits like a glove.
    
Top of the cell is machined, complected, welded and the seams cleaned up on the lathe....
     
The top is centered on the main chamber and welded, supporting from the top end on the lathe with a live center, the seams are cleaned and the cell is
polished up.
The details are assembled and the "STAMMZELLE" is complete.....ready for the generation of hard experimental data
[Edited on 8-2-2017 by markx]
Exact science is a figment of imagination.......
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