fig, 1, the ddt chain, - fas

14
.7 .; . ‘- “’@~~-79-3106 mm PRIMER ON SDT, DDT, XDT , PICKUP, AND SYMPATHETIC DETONATION AUTHOR(S): LCMlis C . Smith Bobby G. Crkdg SUBMl17ED TO: l(3thJANNAF Combustion Meeting September 10-14, 1979 Naval Postgraduate School, Monterey, CA BY aastenm of this rticle, M wblishe~ -x@s- that the U.S. Goverrwnent rettins nonesrclusive, royaltwfme license to publish or reprodum the publislmd form of this contribu- tion, or to allow others to do so, for U.S. Gowrnrnent pur- @ses. The Los Alamos Scientific Labomtory requmls that the pub- hsher identify this rticl M work performed under the u8- p,cmof meus. cmiertment of Enewv Mii!!lR LOS ALAMOS SCIENTIFIC LABORATORY PostOffIceBox1663 LosAlamos,NewMexico87545 An AMnnaWe Action/Equaf OppurhmWEn@ww Form No. S3S R3 St. No. 3S29 Itim UNITED STATES OE?ARTMENT OF ENS?RG~ CONTWACT w-74n8-EN= ‘a

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.7—.; .

‘- “’@~~-79-3106

mm PRIMER ON SDT, DDT, XDT , PICKUP, AND SYMPATHETICDETONATION

AUTHOR(S): LCMlis C . SmithBobby G. Crkdg

SUBMl17ED TO: l(3thJANNAF Combustion MeetingSeptember 10-14, 1979Naval Postgraduate School, Monterey, CA

BY aastenm of this ●rticle, M wblishe~ -x@s- that the

U.S. Goverrwnent rettins ● nonesrclusive, royaltwfme license

to publish or reprodum the publislmd form of this contribu-

tion, or to allow others to do so, for U.S. Gowrnrnent pur-

@ses.

The Los Alamos Scientific Labomtory requmls that the pub-

hsher identify this ●rticl M work performed under the ●u8-

p,cmof meus. cmiertmentof Enewv

Mii!!lRLOS ALAMOS SCIENTIFIC LABORATORYPostOffIceBox1663 LosAlamos,New Mexico87545An AMnnaWe Action/EquafOppurhmWEn@ww

Form No. S3S R3

St. No. 3S29

Itim

UNITED STATES

OE?ARTMENT OF ENS?RG~CONTWACT w-74n8-EN= ‘a

About This Report
This official electronic version was created by scanning the best available paper or microfiche copy of the original report at a 300 dpi resolution. Original color illustrations appear as black and white images. For additional information or comments, contact: Library Without Walls Project Los Alamos National Laboratory Research Library Los Alamos, NM 87544 Phone: (505)667-4448 E-mail: [email protected]

PRIMER ON SDT, DDT, XDT, PICKUP, AND SYMPATHETIC DETONATION*

Louis C. Smith and Bobby G. CraigUniversity of California, ItosAlamos Scientific Laboratory,

Los Alamos, New Mexico 87545

When Bob Craig asked me co give this talk, what I agreedto was to present an elementary discussion of DDT and SDT.When I received the printed program I was surprised to discoverthat my assignment had broad&ed considerably:time will come to my rescue. There is only soin thirty minutes, especially about a topic weabout anyway. Besides, I only have to get thevarious aspects of the subject will be coveredother papers to follow.

Fortunately,much one can saydon’t know much-ball rolling;in detail in

The C-4 movie shown by LeRoy Throckmorton presents aspectacular example of a chain of events that underlies essen-tially all accidental detonations. The chain, in a reasonablycomplete form? is shown in Fig. 1. We can erter the chain --that is, an accident can start -- at any cne of the boxes.

ICHARGE

BREAKUP

SHOCK

c

SHOCK-DETO-

> FORMATION NATION TRAN-

SITION (SDT)

IGNITION ~ DEFLAGRATION-DETONATION+—> TRANSITION (DDT)

FIG, 1, THE DDT CHAIN,

I will first describe the chain qualitatively, proceeding fromleft to right because that’s the way things happen in reallife. I will then try to summarize what we know about the in-dividual links in the chain. For that I will take them inrevers~ order because our knowl~:-ijedecreases rapidiy as we gofrom right to left.

We start with two events, charge breakup and ignition,that may occur simultaneously or in either order. What is re-cruiredis that we obtain rapid ignition of a sufficientiJ*largesurface to support the rest of the process.---------------------------

*Sponsored by the U.S Deprtment of Energy, Contract W-7405-ENG. 36.Approved for public release; distribution unlimited.

4

The word in the next box, deflagration, means differentthings to different people. To me, in this context, it impliesa rapid and rapidly accelerating combustion process. The de-flagration must result in the formation of a shock wave some-where in the system. If the shock is sufficiently intense andconditions are otherwise favorable, a shock-to-detonation tran-sition (SDT) will occur and the entire charge will be consumedin a matter of microseconds. The last three boxes togetherform a deflagration-to-detonation transition (DDT).

Let us now retrace our steps and discuss the various ele-ments in the chain in greater detail. Much of what I will sayis controversial or speculative, so if the person next to yousnickers at my way of explaining something, it’s probably be-cause he thinks he could do it better - and maybe he could.

This talk is supposed to be a primer, so before I discussSDT I will say just a few words about detonations in condensedexplosives. A detonation wave is an intense, reactive shockwave which travels through the explosive at a velocity typical-ly in the range of 5000 to 9000 m/s - some two to three timesthe longitudinal sound velocity in the unreacted material. Thefront of the shock compresses the cold explosive, heating it toa temperature such that it decomposes in a microsecond orless. In decomposing, the explosive releases some 1000 to 1.500cal/g of energy and a large volume of gas, about a liter pergram, which serves as the working fluid when the products dowork t~il their surroundings. At the completion of reaction, atwhat is called the Chapmzn-Jouguet or C-J point, the tempera-ture is about 3000 K and the pressure several hundred kilo-bars. The detonation velocity usually increases linearly wit’]density with a slope of around 3200 m/s for each g/cm3 in-crease in density. The detonation pressure increases approx’.-mately as the square of the charge density, which is why higndensit~ is important in some applications of explosives.

Obviously, not all shock waves that travel through an ex-plosive charge are detonation waves. More generally, the non-reactive shock waves in any m~terial define what is called tileHugoniot of the material. Hugoniots frequently take the form

us = co + sup

w;~ereUs is shock veloci~y, CQ is the bulk sound velocity,s is a coefficient, and Up is the particle velocity associ-ated with the shock (the particles acquire kinetic energy whena i;hockwave passes through). However, Huganiots are notal~ays linear in the Us-U plane. They may curve gently,or ~hey may exhibit abrup? changes in slope. The latter usual-ly signifies that a phase change has Gccurred.

Hugoniots are determined experimentally; Jerry Dick willdescribe one way of doing so in his paper on the wedge test to

be given tomorrow aftexnoon~ Used with relations derived fromthe conservation of mass, momentum, and enerqv, the Hugoniotprovides a description of the hydrodynamic and thermodynamicstate of the explosive behind a shock wave (an equation ofstate is also needed for a complete description) .

Some shock waves may cause incomplete reaction of the ex-plosive. Except in rare cases, this represents an unstablesituation. If the shock is intense enough, it will accelerate(build up) and become a detonation. otherwise it will decayand fade away. A very useful approximation that works in2manysituations is called the single-curve buildup hypothesis.It relates pressure and distance of run, as shown in Fig. 2.The hypothesis states that the buildup process will follow thiscurve, from left to right, no matter where on the curve theprocess starts.

An actual example is shown in Fig. 3. This is a plot ofdata from four experiments on FKM. The origin of the time axisis the time at which detonation occurs. The solid symbol ineach case gives Us and t for the entering shock for that ex-periment; the remaining symbols of each type then describe the-.buildup of that shock.- There is evidence in this example of a

P

OR

11~

P.

P(-J

.—XORT X*

Fig. 2. Buildup curve..-

*In the absence of experimental data, the Hugoniot of an or-ganic explosive can be estimated from its molecular structureand density by means cf a generalized Hugoniot. See, forexample, Ref. 1.

7

6

5

4

3

2

.,

-21 , I , , I 1 t , I I * I , 1

-6 -5-

FIG, 3, TEST OF

-4 ‘ -3

T (US)

SINGLE-CURVE BUILDUP HYPOTHESIS

-i o

FKM ,

slight departure from the single-curve hypothesis; the squareslie slightly above the circles, the triangles above thesquares~ etc. The agreement is usually better, but I used thisexample because it was readily available in the form I needed.

Another useful relationship connects x*, the buildup orrun-up distancer with Po~ the pressure in the entering shockwave. This relationship is commpnly called the Pop Plot afterAl Popolato~ one of its discoverers.3 It takes the form

X* = b#o

so that Pop Plots are straight lines on log-leg paper. Fromthe Pop Plot and the single-curve buildup hypothesis it is pos-sible to back out the decomposition rate as a function of thelocal thermodynamic state of the explosive. One procedure fordoing thi~ is known as Forest Fire after Charles Forest, itsinventor.

The Pop Plot, which is also determined e~perimentally, iscentral in the SDT process. To see why this is so in a verysimple case, let us refer to Fig. 4. A projectile strikes acylinder of explosive of radius r at the left, sending a shockwave of pressure P. into the explosive.* Initially the wholecross section of the cylinder is at pressure Po, but as soonas the wave starts down the stick, a rarefaction wave travelsradially inward with the local velocity of sound, relieving thepressure. Thus the area compressed diminishes steadily as thewave proceeds into the charge, as shown by the dotted line, andthe wave essentially vanishes at a distance approximately equalto rUs/C.detonation ~ffl’~ro~~~!~;essure ‘s ‘reater ‘ban ‘us/c’Pop Plots for several explo-sives and propellants are shown in Fig. 5. The one for FKM,for example, tells us that a plane, flat-topped, 40-kbar shockin FKM will build up to detonation in about 10 mm of run.

What’s going on in the explosive while buildup is occur-ring? That is, where does the energy come from that causesSDT? The temperature behind a 40-kbar shock will be about1700C, far too low for ordinary thermal decomposition to besignificant. The most likely source of chemical reaction----------------------

*Not~ that the pressure of the shock wave in the explosive de-pends on the velocity of the projectile and the Hugoniots ofthe pro-jectileand target - which is one reason it is iniportantto know the Hugoniots.

**For shocks near the “critical” pressure detonation also willnot occur if the diameter of the shock becomes less than thefailure diameter of the explosive.

‘\PROJECTILE

\ \

/+=

~ ‘s <’:> EXPLOSIVE

/ti

Fig. 4. Shock initiation in cylinders.

(energy) appears to be a hGt-spot/combustion process. Voidsand density discontinuities perturb the shock and produce mi-croscopic regions of very high temperature and pressure inwhich decomposition is almost instantaneous. These small re-gions then burn outward. As the pressure increases the burn-ing rate increases, and initially the burning area also, sothat the process is an accelerating Gne. Eventually the tem-perature may become high enough for thermal decomposition toocc~lralso. If conditions are riqht, the wave ultimately be-comes a detonation wave.

The question is, Is this model plausible? In Table I Ihave listed a set of conditions that would suffice ior a 20-kbar shock .inPBX 9404 (94/3/3 - HMX/NC/CEF). ‘l’hedecomposi-tion rate, A , is obtained from the Forest Fire rate law. Theburning rate, r, is obtained by extrapolating data obtained onHMX at lower pressures. The burning area follows from A andr. I have taken 7 ~m for the hot spot radius for reasons Iwill mention shortly; too large or too small a value leads tounreasonable results. I can then calculate the number of hotspots/cm3 required to give the necessary combustion rate. IfI assume that the HMX particles are uniform 60-um spheres, Ihave 2.6 hot spots per HMX crystal; somewhere around 1 or 2would seem about right, so that’s not too bad. If they weredistributed uniformly on a cubic lattice the hot spots would be35 vm apart, center to center. The hot spots occupy 3.3% ofthe volume of the explosi~~e. From data by Ramsay and cal-cu~ations by Mader~ Z es!.imate3% ~ecomposition behind a20-kbar shock in PBX 9404. It was for that reason that I chose7 iimfor the hot-spot radius (the hot-spot volume isproportional to the assumed radius).

The last line of the table is an estimate of flamethickness derived from information provided by Chan Price ofNWC. Most people ignore this factor in discussing the com-

2(

lC

>,4

3

2

110

FKM

9404(1.84)

PETN(1,72)

I I I

20 30 40

P (KBAR )

60 80 100

FIG, 5, 3“F’u~ PLOTS (DENSITIES IN G/CM GIVEN IN

PARENTHESES),

.

TABLE 1. A Hot-Spot Model for PBX 9404.

i= o.02/wr (20 kbar, 100oc) =

4.4 x 10-4 cm/~s

Burning area = 140 cmHot-spot radius (assumed) = 7 UrnNo. of hot spots/cm3 = 2.3 X 107No. of hot spots/60-Vm HMX crystal = 2.6Hot-spot separation, center to center (ave) =3511mHot-spot volume/cm3 = 0.033 cm3Hot-spot energy = 85 cal/cm3Flame thickness (est) = 0.5 ~m

bustion model, but it seems evident to me that, for a flame toexist in a hot spot, the flame thickness must be less than thehot-spot radius. There seems to be no problem with this ex-ample. However, it is tempting to speculate that the reasoncertain explosives, such as NQ and TATB, are so insensitive toshocks is because their flame thickness is always too large, sothat this model cannot provide the necessary growth. Shockinitiation will then depend on thermal decomposition, and thisin turn will require much higher shock pressures.

One cariquibble with the manner in which I have construc-ted Table T, but my own conclusion is that for most explosivesthe hot-spot/combustion model will protide the observed decom-position rates with credible values vf the various physicalquantities. Note that this model applies only to nonhomogene-ous explosives; liquids and single crystals conform to a quitedifferent model.5

1 have now discussed the last box in Fig. 1, having de-scribed both the qualitative features of SDT and a model thatseems to work. Proceeding to the left, we come to the onelabeled shock formation. Our problem here is to explain in aphysically plausible way how a combustion can lead to the for-mation of a shock of some tens of kilobars. Obviously, com-bustion under heavy confinement can lead to very high pres-sures? but uniform high pressure is not a shock wave. What isrequired is a sufficiently high rate of rise in the pressure.

In discussing this, nearly everyone sooner or later getsaround to drawing something like Fig. 6. At the left we startout with a ramp wave, with a steep pressure gradient. Soundvelocity increases with pressure, so that the higher pressureparts of the wave travel faster than the lower pressure par+~.The result is that after some distance (or time) the wavesteepens and becomes a shock, as shown at the right. The shockmust form before a signal can get back from a free surface orbefore the wave reaches a free surface. Otherwise, the pres-

P

x

FIG, 6, SHOCK FORMATIONFROMA RAMP WAVE,

sure is relieved and a shock never forms. We can thus see in aqualitative way that:

a) The steeper the gradient, the more rapidly theshock will form.

b) The time available for shock formation increaseswith the size of “thesystem.

Not so obvious, perhaps, is that to reach the pressures re-quired we usually have to depend on the inertia of the systemto provide the necessary confinement.

It is beyond the scope of thi~ paper to discuss analyti-cally how steep the pressure gradient must be. Qualitativelyit would seem as though kilobars in microseconds must be theorder of magnitude required.

As was already noted, to attain the pressures and pres-sure gradients required for SDT requires a rapid and rapidlyacceleratir,qcombustion process - called Deflagration inFig. 1. The necessary rapidity can be obtained by having ahigh enough burning rate and a large enough burning surface ina sufficiently small volume. ‘he acceleration can be obtainedin several ways~ but the increase with pressure pcovided by theusual burning law, cP*, is usually adequate.

Many DDT problems in one and two dimensions can be calcu-lated numerically qiven the properties of the explosive, thegeometry of the system, and the combustion area as a functionof time. An example calculated by Forest is shown in Fig. 7.This is a one-dimensional problem in cylindrical geometry,chosen because it illustrates some of the more interesting fea--tures of the DDT process. Initially we have a porous bed of

D15T9tiCE

DX5TWiCE

‘1

DIST9NCE

FIG, 7, DDT IN A SOLID CYLINDER,

l-D. (S/V). IN POROUS BED = 75/cM,

tlISTWiCE

R (CM/#S) = 0,00773 PO’94*(MBAR) ‘

propellant in the form of an annulus 2.0 cm thick at 90% ofTMD. Outside the annulus is an aluminum case, inside is asolid grain. The surface-to-volumeratio in the porous bed is75/cm; the bed is assumed to consist of uniform sphericalgran-ules. It is further assumed that at t = O the entire surfaceof the porous bed is ignited simultaneously and that the pres-

‘n the bed is 760 atm. The burning law used is 0.007?3~~~845 cm/us with P in megabars. A Forest Fire rate law isused for the solid grain. The top half of each frame gives themass fraction of propellant remaining. The lower gives thepressure as a function of position: the scale varies as shownin the lower right-hand corner. The time in micros~conds isgiven in the lower left-hand corner.

In the first frame, at 10 us, a ramp wave is moving intothe solid grain. AC 40 vs the maximum pressure is about 14kbar, and we’re beginning to see some decomposition i ] thesolid grain. At 50 pa the maximum pressure is over 50 kbar andthe wave has steepened into a shock. Note that decmnpositionin the grain is now occurring mostly at the shock front. At51..7pa detonation occurs at a radius of a~out 9.5 cm. Decom-position in the porous bed is still only 20% complete.

In cylindrical geometry convergence of the wave may bevety important in the buildup process. In fact, in 1-D calcu-lations such as this detonation will always occur in a solidgrain. Real motous, of course, have center bores, so the cal-culations are more meaningful for such casns.

A much more difficult problem is that of calculating therate at which the flame penetr~tes a porous bed; we sidesteppedthat in the example above. I expect we will hear somethingabout this this afternoon in the paper by Hopkins et al. Theseare certainly noble efforts, but I sometimes wonder if ic willever be possible to include all the physics - such as the ef-fect of turbulence in the hot gas, for example.

We are left with the two boxes at the extreme left ofFig. 1. As we have seen, breakup of the charge is needed inorder to obtain a high enough surface-to-volume ratio for thenext step-in the chain. Breakup of the degree requi-ed usuallyoccurs by impact or shear. Materials scientists are trying totreat these processes ~nalytically, but they have a very toughrow to hoe! As to ignition, it may already be present, as inLeRoy’s examples, or it may be provided by any one of a numberof processes that produce a local concentration of heat.Although superficially the concepts seem simple enough, igni-tion and flame-spreading again pose some difficult analyticalproblems. In the case of ignition of a solid by a hot gas forexamplel surface roughness may be of paramount importance.6We’ll hear more about these matters tomorrow morning.

*

As I suspected, my time is almost up and I still haven’tgotten to XDT, pickup, and sympathetic detonation. I have toldyou much of what you will need to know to understand the quali-tative features of these processes, however, and all will becovered in talks to be fiivenlater on today. I will make a fewcomments r~garding how these processes are related to my Fig. 1.

In the simplmt case of sympathetic detonation, not in-volving fragments, we enter the chain at the penultimate box.The air shock and the motion of the detonation products fromthe donor charge establish a ramp wave in the acceptor charge.‘!?heramp quickly becomes a shock, and SDT follows. Problems ofthis sort are susceptible to numerical analysis, as Al Bowmanwill tell us ‘.]isafternoon.

Sympathetic detonation by fragments is another matter en-tirely except for certain special cases that can be treated asone- or two-dimensional SDT problems. The more usual cases re-quire two- or three-dimensional treatments of the entire chain,starting with charge breakup and ignition by fKiction or vis-cous flow. Needless to say, the empirical approach predomin-ates here.

XK)Tand pickup are newly coined terms. So far as I know,XDT doesn’t have a generally accepted definition. It is under-stood to represent a process similar to SDT, but which occurson a longer time scale - after first passage of the initialshock wave. It might also be a very rapid DDT. Pickup usuallyrefers to experiments in which one piece of ,propellant,firedfrom a gun, strikes a second piece located a short distancefrcm a target plate. The second piece is,damaged by the in-pact, and both pieces then strike the tz~get plate. The pur-pose is to determine whether DDT occurs more readily in freshlydamaged propellant. These two phenomena presumably enter thechain at Charge Breakup and then proceed through Ignition on tolleflagration. I believe we will hear about bcth later on thismorning.

REFERENCES

1. A. N. Afanasenkov, V. M. Boqomolov, and I. M. vc)sk~bc)inikcjv,“Critical Initiation Pressures of Explosives;” in “Control ofNoxious Gases in Blasting Work, and New Methods of TestingIndustrial Explosives,” B. D. Rossi, Ed. Translation avail-able from U.S. Department of Commerce, National TechnicalInformation Service, Springfield, VA 22151.

2. C. L. Mader, “rhe Two-Dimensional Hydrodynan.i.cHot Spot, VolII,” Appendix I). Los Alamos Scientific Laboratory reportLA-3235 (1964).

3. J. B. Ramsay and A. Popolato, “Analysis of Shock Wave andInitiation Data for Solid Explosives;” in “Proceedings of theFourth Symposium (International) on Detonation.”

4. C. L. Mader and C. A. ~orest, ‘;Two-DimensionalHomogeneousand Heterogenecws Detonation Wave Propagation.” Los AlamosScientific Laboratory report LA-6259 (1976).

5. A. W. Campbell, W. C. Davis, and J. R. Travis, “Shock Initia-tion of Detonation in Liquid Explosives.” Phys Fluids ~, 498(1961) .

6. E. E. Kiselev, A. D. Margolin, and P. F. Pokhil, “Shoc~ Igni-tion of Po.,ders.”Fiz Goreniy~ i Vzryva 1(4), 83 (1965).— -—