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Danger with Deteriorating Powder
Much of the .30-06 ammo loaded in WWII (about 70 years ago) with stick powder is still quite reliable, IF it has been stored in reasonable environmental conditions. Also, some of the powder from the pull-down ammo is still usable. However, some powder is also showing signs of significant deterioration and should not be used. I have had a couple experiences with deteriorating powder.
The first one described was with once-fired, relatively new, commercial Remington and Winchester brass in 7 X 57 Mauser. The problem was definitely the deteriorated stick powder, not some extremely old, brittle brass.
On July 4, 2003 I fired some 7 x 57 cartridges that I had loaded with BL-32 military surplus stick powder (roughly equivalent to 4895) in 1984 (yes, 19 years before shooting them). I had noticed some time before the loading (or perhaps a few years later) a few "rust" specks in the bulk powder. In 1984 the powder did not have the odor of original solvents or acid, as I recall. Note the picture below and the descriptions of what happened when I fired the ammo.
Case #1 Second round of 5-shot group with Remington brass, first reload, 44 gr. BL-32, 120 gr. Sierra bullet, grouped 0.52" at 50 yards. Case neck "cut" halfway through near shoulder/neck junction. (Looks about like someone had taken a hacksaw to it.) Other four cases look OK. Average velocity was 2826 ft/sec but with 114 ft/sec extreme spread.
Case #2 First round fired with case that showed a very short vertical neck split before firing. After firing the vertical split is much longer and a horizontal split is starting at the shoulder/neck junction (This also happened to be where the base of the bullet was.) Winchester brass, first reload, 42 gr. BL-32, 130 gr. Speer PSP.
Case #3 Second round fired with same load. Case "lost" its neck. Apparently up the bore WITH the bullet. (Yes, I checked the chamber and bore.)
Case #4 Third round fired with same load. Case neck separated and stuck in forward end (note taper) of chamber. The case neck was easily retrieved with a bronze bristle brush.
Please note, before I fired this ammo in 2003 all loaded cartridges appeared quite normal on the outside. Although scientifically interested in what was going on, I quit shooting out of concern for my own safety, and the condition of my rifle. When I got home I pulled the bullets from the remaining loaded rounds. Interestingly, when the bullets were pulled there was sometimes a "pop," either from very negative or positive air pressure in the case. Also, on the inside of the case between the bullet base and the powder there was considerable green, sticky crud. The bullet bases also showed considerable corrosion. The powder clumped pretty badly. If I remember correctly, some of the loaded rounds had been stored in plastic boxes with the bullets up and these (Remington brass) did not deteriorate QUITE as badly as those stored horizontally in typical 20-round cardboard boxes. Regardless, loading stick powder that has started to deteriorate is asking for trouble. Apparently, the acidic fumes and/or other chemical reactions served to corrode and/or make the brass very brittle.
Deteriorating powder can cause serious separations and splits in the cases. It is possible that excessive pressures could result. However, my chronograph data did NOT indicate unusually high velocities.
DO NOT LOAD STICK POWDER THAT IS STARTING TO DETERIORATE!!
# # # # # # # # #
Following are 3 pictures that show the effects of deteriorated powder on some .30-40 Krag ammo. I examined the ammo and took the pictures in 2007. I did not try to shoot any of it, and I did not record with the pictures the date it was originally loaded with the BL-32 stick powder. As you can see from the first picture all 10 rounds were not affected equally, but ALL were UNSAFE to fire, even the best-looking ones that could have had the outside of the case “cleaned up” of the tarnish. I was not going to fire any of this batch in my Krag rifle, and I sure as h*** would not try to pass them on to another Krag rifle shooter!!
Numbering from left to right, note that the #2 and #5 cases were so badly corroded that the bullets broke off with the case necks around them when they were pulled!! Case #6 was also badly corroded in the neck-shoulder area. The bullet had not yet been pulled. The other 7 cases showed some tarnish (#8 & #9 a fair amount of dark tarnish). However, cases #1, 3, 4, 7, & 10 showed very little tarnish, probably not enough to raise a red flag to the casual observer had they been in a separate group of loaded ammo.
This is a closeup of rounds #5 and #6 (as numbered from left to right in the first picture of all 10 rounds). You obviously could not shoot round #5, and anybody with common sense would not likely try to shoot #6. Please note the small spot of corrosion at just about the position of the top of the “solid web” of case #5. You can see it really well on case #6. And, yes, this corrosion (as well as the obvious corrosion at the base of the necks on cases #2 and #5) started from the inside of the cases. Firing a round with such corrosion that low on the case could be extremely dangerous.
This is a closeup of one of the best-looking rounds. I am not sure which one of the 10, but a casual observer of the loaded round would probably not have suspected what it looked like inside and the possible danger in firing it. Note the tarnish/corrosion on the outside of the case near the neck-shoulder junction. Note the green crud sticking to the inside of the case where the base of the bullet had been. Note also the powder grains “sticking” to the inside of the case just below where the base of the bullet had been.
Thank you for the write up. I had always been told to be really concerned if the cases showed "pink" corrosion but everything else if it was not caked on could be cleaned off and used.
I agree with you on the old .30/40 loads with the corrosion. However, your problem with the 7x57mm loads may not have been powder related. You may have had a bad batch of brass.
The link to the slideshow will show some .223 loads I made up using mixed once fired military brass, WSR primers, fresh AA2520 powder and WW 55 gr. FMJ bullets. Firing them in an AR15, I experienced a failure to go into battery and found the case neck of the previous cartridge had lodged in the chamber. It came out on the bullet of the round that wouldn't go into battery. This happened two more times so I stopped shooting. There were no signs of excessive pressure. These loads were less than 1 year old.
Some of the necks of the loaded rounds would snap off under thumb pressure. I pulled the remaining rounds to double check my loading. All were as intended with, IIRC, 26.0 grs. AA2520. I posted all this on the CMP forum back in 2008 and no one could determine the problem other than poorly annealed brass.
Years ago I encountered brittle, splitting necks on the first firing with a batch of new 7x57mm RP brass. These loads used the starting charge of fresh IMR 4064, WLR primers and RP 150 gr. bullets. The whole box of 100 new brass were brittle. When testing the new, unloaded brass with a pair of pliers the necks would crack and split instead of just flattening. I have never bought RP brass since.
If anyone has any comments or insight on the failure of the OP's or my brass please chime in.
I was not trying to hijack this thread but my above experience was identical, or at least similar, to the OP's.
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Last edited by sigman2; 01-30-2015 at 10:45 PM.
I have no idea what BL-32's composition is/was. I didn't find an MSDS for it in a brief search. So I went with something I am familiar with - IMR-4895.
'4895 is a single base powder, composed mostly of nitrocellulose (NC), with some diphenylamine (DPA), dinitrotoluene (DNT), and potassium sulfate.
DNT is your burn-rate modifier. It's something that varies greatly in at least the IMR stick powders (from 4-15% or so total weight). Potassium sulfate is a salt - it inhibits muzzle flash. Too much, if memory serves, though, will cause a burn-rate modifier effect. Memory is fuzzy on that one these days, but the sulfate is stable and the DNT is relatively stable as well. "Relatively."
DPA and NC are what we care about. NC is made by adding nitro (-NO2) groups (ester bonds) to cellulose. To do this, the cellulose is mixed and cooked in a bath of water, sufuric acid and nitric acid, creating the ester bonds, then neutralized, and sent on for further use. Despite neutralization, very miniscule amounts of oxides of nitrogen (nitrates) can still remain in the NC, and in the final powder product. When the nitrates mix with air or water, nitric acid can form. In addition, heat (energy input) causes the ester bonds of NC to break down, releasing more nitrates into the mix.
DPA is our hero here. DPA scavenges free nitrates in the closed world of our cartridge or powder container. With no free nitrates to roam about and mix with water vapor, nitric acid formation is prevented - but not forever. Eventually all the DPA is used up, forming other nitrogen compounds. The NC continues to break down over time, forming more and more unbound nitrates in a world full of oxygen and water!
The common nitrogen compounds at this point become nitrogen dioxide (stinky brown gas) and nitric acid (nitrates and water vapor). Nitric acid in a world of zinc and copper (brass) is bad. The acid reacts with the brass alloy, forming copper nitrate and zinc nitrate. Copper nitrate is the pretty blue stuff you found in and on the brass and copper jackets. Zinc nitrate is a whitish crystaline 'fuzz', which is why you often see both the blue color and the whitish fluff in cases like this. The extent and appearance of both will depend on the alloy itself, and the surrounding time and conditions for the ongoing reaction.
Made short and sweet, your primary propellant constituent (NC) is breaking down naturally, faster when there is heat energy involved. The components mix with air and water to form gas and acid. The acid in turn attacks the copper and zinc in the brass, and everything goes to pot.
Sigman2, you make a good case that the failures you described were due to brittle, once-fired military 5.56 brass and brittle new Remington 7 x 57 Mauser brass. (I am assuming in the experiences you described that you did not encounter the signs of deteriorated powder itself or the related corrosion of the brass and bullet bases. Such deteriorated powder evidence was not seen in the pictures you posted.) You may recall my experience with both Remington and Winchester 7 x 57 Mauser cases was that they had been previously loaded and fired with no problems. Only after I reloaded the cases with the BL-32 surplus powder (from the same container and let them set for 19 years) did they show the brittleness of the brass, the corrosion of the brass and bullet bases, and the deteriorated powder itself.
Edwardm, thank you very much for posting the chemical and technical information on such single-base “stick” powders as 4895, particularly when it deteriorates.
Would this information be worthy of CMP forum preservation as a “sticky?” Or, is such information readily available elsewhere? If so, where?
The life time for gunpowder has been called "interminable", which is another way of saying, unpredictable. Gunpowder has a life time, if you ever took thermodynamics you will understand it when I say gunpowder is a high energy compound that is breaking down to a low energy compound, and you will understand why, and why this is perfectly natural. Just exactly when it deteriorates to a useless state is impossible to predict with any certainty, from the outset, but the lifetime of gunpowder is in terms of decades, not centuries. Something else to remember about this, it gets worse and more dangerous with age.
Whether powder is good is not easily answered unless the powder has gross indications of going bad.
The gross indications are the bitter smell due to NOx, red powder granules, fuming gas emissions, others have said “red gas”. By the time you see this the powder went bad a long time before.
Half of all the surplus IMR 4895 I purchased went bad. The first 16 lbs, I used up eight pounds quickly. For whatever reason, I pulled the bullets on some of that stuff and found green corrosion on the bases of the bullets. Similar to these pull down bullets from old US ammunition. Not the horrible one, but the small green spots.
I don't remember what US ammunition these came from I pulled them decades ago.
It took a while till I found reason to use the rest of that surplus IMR 4895. When I opened the bottle top, it smelled bitter, red dust flew above the opening. I decided to get rid of it, but not have it wasted. I gave the jug to a machine gunner guy and he put it in his laundry room. Passing by the laundry room he tossed soiled shorts at the hamper, but missed. The shorts ended up on top of the powder bottle and stayed there overnight. Next day my friend found that escaping acid gas from the bottle had eaten holes in his shorts!! :what: This so unnerved my friend, he poured the powder out over his lawn.
Actually this was the best thing to do, and had I know of the hazards of old deteriorated gunpowder, I would have poured it out on the lawn and not given to him to shoot.
Since then I have had more surplus 4895 powder from a different vendor go bad in the case. Visual inspection of the ammunition revealed green corrosion on the bottom of the bullets and cracked case necks.
This powder never smelt bitter at all. I shot this powder in highpower matches and it shot exceptionally well, but case necks cracked after firing. I also received “funny” retorts and the occasional sticky extraction. The longer the ammunition was unused the more cases necks would split when fired. In time virtually all of the remaining 700 loaded cases experienced cracked case necks without being fired.
This powder is from a FA 11-1898 30-40 Krag cartridge. Obviously it is bad.
I sent an IM expert the pictures of my corroded bullets and pulled Krag red powder, and this is what he wrote back:
The red color indicates that the stabilizer is depleted and the redox reaction is degrading the nitrate ester. (I assume this is a single base gun propellant, and the nitrate ester is NC.) Please dispose of this powder and ammo supply before it starts to get warm or self-heat (via autocatalytic exothermic reaction). This stuff can be a runaway reaction and spotaneously explode in storage.
The cracked case necks are proof that the outgassing of NOx is occurring. The pressure build-up is evidently enough to fatigue the metal at a high stress location in the cartridge case (@ the neck bend). You should also see a bulge in the cartridge base (where the firing pin would strike b/c there is a circular joint crimp there between the two metals). This ammo would explosively vent at the crack if you tried to fire it in a gun. Just like the Garand example you sent. Please discard this ammo.
The corroded ammo is the same as above (redox reaction gassing NOx) except this stuff actually got wet too. Water provides a medium for corrosive acid reactions to result. Please discard this ammo.
Lessons learned -
(1) Ammo has a finite shelf life
(2) Ammo can be dangerous
From what I had read on the internet, which is a repeat of what is said in gun magazines, powder has an “indefinite” shelf life. I think we all remember reading statements to the effect that powder lost energy as it got old, making it essentially benign. This information is not only wrong, it will get people hurt.
Years later I ran into a Naval Insensitive Munitions expert. This IM expert explained that powder is deteriorating the day it leaves the factory. Nitrocellulose decomposes through the reduction-oxidation process, he called it Redox. The expert said “The molecular stability of the functional groups on the organic chain determine the life time of the nitrocellulose molecule.” This guy actually writes and talks like this, he is extremely bright with a PhD in Chemical Engineering.
The bottom line is that nitrocellulose is a high energy molecule that is breaking down to become a low energy molecule. Anyone who has taken thermodynamics will realize that this is obvious, everything is breaking down to a lower energy state, but somehow, shooters have been lulled into thinking that the second law of thermodynamics does not apply to our sport.
Heat accelerates the deterioration/decomposition of powder and the rate is directly proportional to the Arrhenius equation, which is an exponential function. Maybe this is a simpler way to say it: the lifetime of ammunition decreases exponentially as temperature rises. This table is instructive on how quickly heat deteriorates smokeless propellants:
UN manual on ammunition inspection. See section 7.3.
Surveillance and in-service proof - the United Nations[/B
If you read Insensitive munitions literature, you will see that they use high temperature to accelerate aging of smokeless propellants. Keep this in mind as some of the data I am going to show is from accelerated aging tests.
As gunpowder gets older it does not get safer to shoot. Old gunpowder will, and has, blown up firearms. The basic reason is something called “burn rate instability”. For all your cartridges you want a nice and smooth pressure curve. If the burn rate is irregular, because the nitrocellulose powder grain breaks down irregularly, there will be peaks and valleys instead of a smooth pressure curve. These irregularities can interact in such a way that pressures spike. Double based powders are a combination of nitroglycerine (NG) and nitrocellulose, the NG is there for an energy boost, but unfortunately NG causes a new set of problems. NG is apparently not bound to the powder grain but is a liquid and it migrates. NG is wicked to the surface of the powder grain over time, one causal reason, water condensing and evaporating on the powder grain surface. Apparently the evaporating water molecules pull on the NG. I was told that created a NG rich surface. So, even though the total energy of the grain has decreased due to breakdown, the surface is NG rich and that will spike the initial burn rate. Another thing NG does is accelerate the breakdown of the base nitrocellulose molecule by attacking the double bonds holding the NO molecules. Unfortunately all ionic compounds attack those double bonds, water is a main offender because it is always in air, is a polar covalent ion (acts like an ionic compound) and thus you know the reason you were told to store gunpowder in a cold and dry environment. Quality ammunition is manufactured in humidity controlled environments, between 40% and 20% humidity, but they don't go lower due to electro static discharge concerns. Incidentally rust is bad and that rust that came out of those old tin cans accelerated the aging of gunpowder, and I think, is why they went to plastic containers.
There is almost no data on the internet because all that was ever needed to be known about gunpowder aging was determined well before WW2. However ball powders did come out at the end of WW2 and I was able to find this data showing that gunpowder at the end of its lifetime will pressure spike. I asked you remember that heat is used to accelerate the age of gunpowder, so what you are seeing is in fact because of “age”, not heat, but it took heat to age the powder quickly. The IMR is a single based and the WC is a double based ball powder.
INVESTIGATION OF THE BALLISTIC AND CHEMICAL STABILITY OF 7.62MM AMMUNITION LOADED WITH BALL AND IMR PROPELLANT
Frankfort Arsenal 1962
3. Effects of Accelerated Storage Propellant and Primer Performance
To determine the effect of accelerated isothermal storage upon propellant and primer performance, sixty cartridges from each of lots E (WC 846) and G (R 1475) were removed from 150F storage after 26 and 42 weeks, respectively. The bullets were then removed from half the cartridges of each lot and from an equal number of each lot previously stored at 70F. The propellants were then interchanged, the bullets re-inserted, and the cases recrimped. Thus, four variations of stored components were obtained with each lot.
Chamber pressures yielded by ammunition incorporating these four variations were as follows. These values represent averages of 20 firings.
When I discussed pressure problems and old ammunition with a machine gunner buddy, he said that explained the two top cover explosions he had with old Yugoslavian 8 MM ammo. Machine gunners shoot pallets of ammunition and so they are more likely to encounter the occasional overpressure round. The pictures of this Garand blowup with WW2 ammunition has created posts of angry denial from hoaders. http://www.socnet.com/showthread.php?p=1344088 I collected a number of threads with blowups with old surplus ammunition, and it is surprising just how many firearms have blown up with old ammunition, and yet, the shooting community has not figured out the cause. There are a number of posts of pressure problems with the old Greek ammunition on this forum, yet the posters just assume the ammunition was overpressure when it was issued. Something I highly doubt, but what has happened is that as the powder grain has deteriorated, combustion pressures climb. The phenomena is burn rate" instability. A gunpowder grain is assumed to burn evenly, but if the grain has deteriorated unevenly, when it burns you get interacting and conflicting pressure waves. Uneven burn rate is bad, moves the pressure curve slope, and the end result is high pressures. If the powder grain physically breaks down, there will be powder dust in the case and the surface area of that dust is huge compared to the original grain, and that will spike the pressure. Google coal dust explosions and find out the explosive problems that occur with coal dust, or cotton dust as another example. Burn rate instability is a problem for all devices loaded with smokeless propellants, big and small, and a primary reason old solid propellant rockets are taken out of inventory, because too many of them blow up if fired.
So to summarize, powder does not get better with age, heat ages powder fast, old gunpowder will blow up your firearm. Anyone with a $100,000 dollar irreplaceable machine gun should seriously consider the practice of shooting cheap surplus military ammunition. Machine gunners shoot orders of magnitude more ammunition than most people, so as they are burning through a pallet of surplus ammunition, they are more likely to find that statistically improbable bad round. If that cheap surplus ammunition wrecks the registered part of the machine gun, the machine gun is a total loss. The BATF is not your friend in this matter as the policy of the Federal Government is to reduce the number of machine guns in the hands of the public. You blow yours up, guess what, that is considered a good thing, and you have to find another to replace the one you destroyed. Since the total number will always go down, the next one will cost more.
There are more nasty things that happen with gunpowder and I am going to try to approach this section so you understand observed phenomena:
I can’t say it any better than the Dec 2003 Propellant Management Guide:
Stabilizers are chemical ingredients added to propellant at time of manufacture to
decrease the rate of propellant degradation and reduce the probability of auto ignition during its expected useful life.
As nitrocellulose-based propellants decompose, they release nitrogen oxides. If the nitrogen oxides are left free to react in the propellant, they can react with the nitrate ester, causing further decomposition and additional release of nitrogen oxides. The reaction between the nitrate ester and the nitrogen oxides is exothermic (i.e., the reaction produces heat). Heat increases the rate of propellant decomposition. More importantly, the exothermic nature of the reaction creates a problem if sufficient heat is generated to initiate combustion. Chemical additives, referred to as stabilizers, are added to propellant formulations to react with free nitrogen oxides to prevent their attack on the nitrate esters in the propellant. The stabilizers are scavengers that act rather like sponges, and once they become “saturated” they are no longer able to remove nitrogen oxides from the propellant. Self-heating of the propellant can occur unabated at the “saturation” point without the ameliorating effect of the stabilizer. Once begun, the self-heating may become sufficient to cause auto ignition.
Actually there are only a few compounds used as stabilizers, and as the Propellant Management Guide tells us, stabilizers are consumed with age.
This is a good reference on stabilizers,
ROLE OF DIPHENYLAMINE AS A STABILIZER IN PROPELLANTS;ANALYTICAL CHEMISTRY OF IPHENYLAMINE IN PROPELLANTS
They are using heat to age the powder and as the powder ages, the stabilizer content decreases.
The bitter smell and red color (probably nitric acid gas) we see and smell in very old gunpowder is a consequence of not enough stabilizer left to sop up all of the NOx. As NOx escapes it reacts with water to produce nitric acid gas. That nitric acid gas corrodes brass, bullets, weakens brass, is evidenced by cracked case necks, eats up the ammunition containers; nitric acid gas is nasty stuff. I am certain that a cloud of red fuming nitric acid gas is as toxic as any of the chemicals used in WW1 for chemical warfare.
Our Armed Services have stockpile surveillance programs (but each Service does theirs a little differently) and one of the easiest things to show that gunpowder is at the end of its service life is that red fuming nitric acid gas. Of course there are a lot of tests, if you want to see all the different tests the military uses look at Mils Std 286 Propellants, Solid: Sampling, Examination and Testing to be found at https://assist.daps.dla.mil/quicksearch/.
One common test for gunpowder age is placing the suspect powder in an oven at 65 C (150 F) until it fumes. If the sample fumes within 30 days the lot in the field is either chemically tested for the percentage of stabilizer or it is simply scrapped.
This is from a 1969 Symposium:
This is from a 1970 Symposium:
Each service has its own peculiarities, the Navy expert told me they keep master samples in test tubes. In the test tube is a methyl violet paper, if the paper changes color, they track down the powder lot and test to see how much stabilizer is left. If the amount is less than or equal to 20%, the lot is scrapped. I think this is called the Methly Violet test, or Talliani test in Mil Std 286. Page 5-11 of the 2003 Army Logistics Propellant Management Guide provides the protocols for their Stockpile Propellant Program. The trigger for investigation is: "When Master Sample Stability Failure Occurs". The Navy and Army are consistent in that they scrap powders and propellants when the stabilizer decreases from 100% to 20%.
So, what do you do if you don’t have a chemistry lab to check the percent of stabilizer? Well all you have left is the gross indications of seeing fuming nitric acid and smelling a horrible bitter smell. The smell will knock your socks off. If you see or smell fuming nitric acid the powder went bad long ago. The stuff is absolutely unsafe to shoot and unsafe to store. More on the second point later.
This bottle of Vihtavouri N150 is outgassing nitric acid gas and should be poured out at once before it autocombusts!
My Navy expert provided 'rules of thumb' concerning the safe lifetime of double based and single based propellants. The rules of thumb are: Double based powders and ammunition are scrapped at 20 years, single based 45 years. In his words “These 'rules of thumb' are particularly useful when the protocol fails. The protocol can easily fail when workmanship or good housekeeping measures are not followed during manufacture of propellant and/or rocket motor or during storage of the weapon system components, respectively.”
I want to say, given hot storage conditions, sloppy manufacture, the lifetime of your gunpowder can vary considerably. Rules of thumb are best guesses and best guesses are guesses. Sometimes best guesses work out the way you predicted, when they do people will call you a prophet and you will pat yourself on the back for being a genius. When best guesses go wrong, you will wear the dunce cap and wonder what that word “hubris” means.
Take these numbers with a grain of salt, early in the last century the storage lifetime of smokeless powders was considered to be 20 years or less:
Here, Hercules is bragging about Bullseye powder still being good at 25 years.
Army Ordnance Magazine, June 1931, page 445 says:
“Smokeless powder constitutes one of the greatest hazards from a storage standpoint, due to the fact that it is subject to deterioration and at the best cannot be expected to have a life greater than about twenty years…….Master samples of all lots of smokeless powder are under constant observation in the laboratories at Picatinny Arsenal. Should any of these samples indicate rapid deterioration, notification is given at once, and steps are taken to use this deteriorating material within a very short period, if possible, or else withdraw it from service.”
Federal says their ammunition has a ten year shelf life:
Federal Ammunition :
The military does not talk about this, but bunkers and ammunition storage areas have gone Kaboom due to old powder. That nitric acid builds up, creates heat, and the stuff blows up. It blows up inside the case or the shell. All you have to do is Google "Ammunition Depot Explosions" and you will find that, on average, one ammunition dump explodes per month somewhere in the world. This video of one blowing up is quite impressive:
This section is from the Dec 2003 Propellant Management Guide:
c. During the period 1984 through 1997, seven propellant auto ignition events occurred at U. S. Army Material Command (AMC) Installations.
1984: Lake City AAP
IMR powder that was only 5 years old auto ignited and the above round magazine and its contents were destroyed. More than 100,000 lbs of powder deflagrated.
1984: Lake City AAP
The same lot of IMR powder, a fragment quantity isolated and saved for critical production testing, auto ignited two months after the previous fire. Only a small quantity of powder was lost, but another magazine was destroyed.
1985: Blue Grass Army Depot
The local-stocks storage magazine use for demilitarization activities contained high explosives material as well as unmonitored M10 propellant powder. Auto ignition of the powder and its resulting deflagration gradually ignited the other energetic materials present. The earth covered magazine and its contents were destroyed.
1987: Lone Star AAP
Benite was stored in a heated magazine so that it could be temperature conditioned prior to loading into production items. The building became overheated which accelerated the rate of decomposition of the benite to a point that auto ignition occurred. The structure and contents were lost.
1989: Hawthorne Army Depot
8-inch, 55-caliber propelling charges loaded with single-base propellant auto ignited in an earth-covered magazine more than one year after the Navy ordered the lot destroyed due to low stability. The magazine contents of 30,715 lbs of various propellant were destroyed and the magazine was heavily damaged.
1996: Red River Army Depot
Explusion charge assemblies for large caliber artillery rounds, each charge filled with only one ounce of M10 propellant and stored 250 to a box, auto ignited. The earth covered magazine and its contents were totally destroyed.
1997: Hawthorne Army Depot
M9 flake propellant bags that had been removed from 81 mm mortar round were bulk-packed and placed into long-term storage. A container of unstable propellant auto ignited, and all 20,000 lbs of propellant inside the earth covered magazine were destroyed. The magazine was severely damaged. Value of content lost was more than $3,000,000, which the cost to repair the magazine was $164,000.
Military Surplus Powder autocombusting
1. 10-02-2009, 11:02 AM#6
Last edited by Slamfire; 03-04-2015 at 01:25 PM. Reason: Added, deleted, moved material around, and probably made it more confusing.
Yes, very well done Slamfire. And, thanks to CMP for making this thread a "sticky thread."
Having the thread "sticky" is especially relevant considering all the old and newer military surplus powder and ammo so many of us have and will use. And, of course, much of this information is also applicable to a lot of commercial products.
Thanks for the nice words. The shooting community is basically ignorant of the thermo chemistry and problems with deteriorating gunpowder. We all get our information from Gun magazines and books written by the same authors. Well it turns out, these guys don’t have a technical background in anything, knowledge is not as important as spinning a good yarn. The industry as a whole has a financial reason not to teach you to not to buy old product, so, even after decades of reading the popular press and reloading, it was a total surprise to run into an Insensitive Munitions expert and find that my expectations that gunpowder lasts forever were totally wrong.
Knowledge is power, the power to understand, plan, and protect yourself. Old gunpowder has its risks, once you understand what to look for, you can spend your money wisely.
Last edited by Slamfire; 03-04-2015 at 03:37 PM.